We are grateful for the generous support from our industry partners.
The list of sponsors is in alphabetical order within the sponsorship level.
Please click on the company logo to find more information about our industry partners.
Gold Sponsor
Booth: 49/50
Instem is a global provider of leading software solutions and scientific insight services that is helping clients to bring their life enhancing products to market faster, transforming the future for the benefit of everyone. We enable organizations in the life sciences to collect, report and submit high quality regulatory data more efficiently, while offering them the unique ability to generate new knowledge through the extraction and harmonization of actionable scientific information. Our intelligent solutions empower collaboration and life enhancing science.
Silver Sponsors
Booth: 11
For over 70 years, Charles River has served the world’s industries by
- supporting 86% of novel FDA approved drugs in 2021
- helping 1000+ industrial chemicals reach the market
- assisting in the approval of 34+ agrochemical actives.
Our scientific experts leverage an expansive safety assessment portfolio, a range of laboratory support services, and global state-of-the-art facilities to produce the quality data you need to optimize your product development program - every step of the way.
Booth: 30
CN Bio’s aim is to transform the way human-relevant pre-clinical data is generated to improve drug discovery efficiency. Our PhysioMimix™ OOC range of microphysiological systems & services enable researchers to predict human liver responses to acute & chronic drug exposure in the presence or absence of disease using single- or multi-organ liver-on-a-chip models. By recreating human physiology in vitro, PhysioMimix OOC provides high-content, predictive data that translates between lab and clinic.
Booth: 47
Clear and confident healthcare decisions begin with questions. At Labcorp, we’re constantly pursuing answers. With unparalleled diagnostics and drug development capabilities, we accelerate innovation and provide insight to improve health and improve lives. Whether you’re a patient, provider, researcher or in the pharmaceutical industry, we’re here for you. Learn more at www.Labcorp.com or follow us on LinkedIn and Twitter @Labcorp.
Booth: 3
LGC provides a comprehensive portfolio of biologically relevant models, including patient-derived cancer organoids, reporter-labeled cells, and an unparalleled collection of cancer cell lines from the world's largest biorepository, ATCC. LGC manufactures TRC's uniquely large range of research chemicals, including bioactive molecules, SILs, modulators of angiogenesis and apoptosis, as well as biological targets such as protein kinase and cytokine receptors.
Booth: 33
Welcome to MultiCASE, Inc. - Computational Toxicology Specialists -
For 25 years, MultiCASE has developed state of the art cheminformatics tools and computational toxicology software platforms for evaluating biological activity and toxicity potential for chemicals. Our software applications are used by regulatory agencies, pharmaceutical, chemical, and cosmetic companies worldwide. Consulting and licensing services are provided to fulfill REACH requirements or ICH M7 Step 2 compatible in silico evaluation for drug candidates, impurities, and reagents.
Whether you’re engaged in exploratory research or decision-making within the regulatory landscape, our goal is to create software tools to complement your decision making expertise throughout a risk assessment.
Booth: 23
As a global company with operations across Asia, Europe, and North America, WuXi AppTec provides a broad portfolio of R&D and manufacturing services that enable the pharmaceutical and healthcare industry around the world to advance discoveries and deliver groundbreaking treatments to patients. Through its unique business models, WuXi AppTec’s integrated, end-to-end services include chemistry drug CRDMO (Contract Research, Development and Manufacturing Organization), biology discovery, preclinical testing and clinical research services, and cell and gene therapies CTDMO (Contract Testing, Development and Manufacturing Organization), helping customers improve the productivity of advancing healthcare products through cost-effective and efficient solutions. WuXi AppTec's open-access platform is enabling more than 5,950 customers from over 30 countries to improve the health of those in need – and to realize the vision that "every drug can be made and every disease can be treated."
Bronze Sponsors
Booth: 42
GenoSafe is an analytical CRO providing testing services for the evaluation of quality, safety and efficacy of Gene and Cell therapies. GenoSafe brings its 20-year experience in the development, qualification and validation of analytical methods to perform preclinical biodistribution, shedding and immunogenicity studies according to Good Laboratory Practices – GLP.
GenoSafe will also provide its continuous support for clinical bioanalysis of patient samples (i.e immunogenicity, biodissemination and gene expression studies) as well as QC testing of your drug candidates.
Booth: 54
Inotiv, Inc. is a leading contract research organization specializing in nonclinical and analytical drug discovery and development services. The Company focuses on developing innovative services supporting its clients’ discovery and development objectives for improved decision-making and accelerated goal attainment. The Company’s products focus on increasing efficiency, improving data, and reducing the cost of taking new drugs to market. Visit inotivco.com for more information.
Booth: 26
Lhasa Limited is a not for profit organisation. At Lhasa, we are driven by our purpose; To enable informed decision making on chemical safety. In line with this purpose, we create cutting-edge software solutions, which have been solving real-world chemical safety assessment problems for almost 40 years. Our technology is designed by scientists, for scientists, in collaboration with industry stakeholders and regulators. We are committed to enabling scientists to make better predictions on the safety of drugs, chemicals and cosmetics by using existing data better and developing computer-aided reasoning and information systems for the advancement of science.
#visitljubljana
Booth: 29
About VIMTA:
Founded in 1984 with headquarters in Hyderabad, India. Vimta Labs is a leading contract research and testing organization with 19 satellite labs across India with a wide and global span of services to support Pharmaceuticals, Food, Electronics, Health Care, and other industries. VIMTA has been supporting many national and overseas businesses for close to four decades for their third-party testing, research, and outsourcing needs.
Our service portfolio includes analytical, clinical, and preclinical services to life sciences industries; providing an integrated scientific, technical, and regulatory expertise to support all stages of drug development and manufacturing process for small & large molecules.
We have a track record of strict compliance to regulatory requirements (cGMP, GLP, GCP) & Standards (ISO 17025, ISO 15189, ISO 9001), and have undergone numerous audits successfully from regulatory agencies across the globe.
Sponsors
Booth: 46
acCELLerate is a specialist for large-scale preparation of Assay Ready Cell Banks for small molecule drug discovery (HTS), ADME-Tox, and potency testing of biotherapeutics. Assay Ready Cells are used instantly after thawing without prior cultivation – basically like a reagent. This approach increases the flexibility and improves the precision of a cell-based bioassay.
Elsevier is a global leader in information and analytics that helps researchers and healthcare professionals advance science and improve health outcomes for the benefit of society.
We publish several of the leading books and journals in the field of toxicology, including our open access journals Toxicology Reports, Current Research in Toxicology and Toxicon. We are proud to support Eurotox.
Booth: A9
European Publishing is an Open Access Publisher of 6 peer-reviewed journals (including the journal Public Health and Toxicology, a media partner of the EUROTOX 2023 conference).
Based in the Science and Technology Park of Crete, one of the main units of the Foundation of Research and Technology, European Publishing adheres to ICMJE and COPE guidelines, supports the THINK-CHECK-SUBMIT initiative and has been responsible for its official translation into two European languages. It is supported by the European Union Regional Development Fund, and it is also a proud member of OASPA, ALPSP and ELEVATE GREECE.
The Glyphosate Renewal Group (GRG) is a collection of companies that seek the renewal of the EU authorisation of the active substance glyphosate in 2023 by joining resources and efforts to prepare a single dossier with all the scientific studies and information on the safety of glyphosate.
SUN bioscience is enabling personalized medicine through its SUN’s proprietary high-throughput 3D microwell platform.
Our flagship technology Gri3D® is solving the challenges of organoid culture: automation, robustness, scalability, and easy imaging. This will introduce a new era in drug development.
TEAM mastery is a leading service provider in the area of chemical regulatory affairs, covering all aspects of REACH, Biocide Product Regulation, medical devices, plant protection products (PPP) and other regulations related to safety assessment of chemicals. Our team is composed by highly motivated people with specific expertise in chemistry, toxicology, environmental toxicology and risk assessment. We are committed to assisting customers, helping with the cost-efficient implementation of European and global regulations on chemicals. Our approach is focused on advanced solutions, that combine a scientific approach with regulatory needs to gain the highest benefit for industry and the downstream users.
Mediline is a Slovenian company that specializes in supplying high-quality laboratory equipment,consumables and diagnostic reagents.
Republic of Slovenia
Ministry of Agriculture, Forestry and Food
Republic of Slovenia
Ministry of Health
Exhibitors
The list of exhibitors is in alphabetical order.
Please click on the company name to find more information about our industry partners.
Booth: 43
ACCELERA is a Contract Research Organization currently collaborating with more than 300 Sponsors worldwide with a strong focus on safety studies for multiple emerging modalities.
ACCELERA supports all stages of drug discovery and development offering tailored services spanning across different disciplines, including General and Developmental and Reproductive Toxicity studies, safety pharmacology, early formulation development, preclinical metabolic profiling, bioanalysis and pharmacokinetics (PK).
ACCELERA has a unique platform of integrated scientific, technological and regulatory expertise, built on decades as part of the international pharmaceutical industry.
Booth: 45
acCELLerate is a specialist for large-scale preparation of Assay Ready Cell Banks for small molecule drug discovery (HTS), ADME-Tox, and potency testing of biotherapeutics. Assay Ready Cells are used instantly after thawing without prior cultivation – basically like a reagent. This approach increases the flexibility and improves the precision of a cell-based bioassay.
Booth: A4
Altasciences is an integrated drug development solution company offering pharmaceutical and biotechnology companies a proven, flexible approach to preclinical and clinical pharmacology studies, including formulation, manufacturing, and analytical services. For over 25 years, Altasciences has been partnering with sponsors to help support educated, faster, and more complete early drug development decisions. Altasciences’ integrated, full-service solutions include preclinical safety testing, clinical pharmacology and proof of concept, bioanalysis, program management, medical writing, biostatistics, clinical monitoring, and data management, all customizable to specific sponsor requirements. Altasciences helps sponsors get better drugs to the people who need them, faster.
Booth: 40
AlveoliX provides advanced in-vitro models, called Organs-on-Chip. These models are used to better predict human responses in preclinical drug development and to gain more insight into human biology. We offer equipment and consumables to run organ-on-chip experiments in your laboratory. We also provide services for drug safety and efficacy testing on advanced in-vitro systems for discovery and preclinical phases. In addition, our team of experts in engineering and in-vitro modeling supports you with study design, biomodel development and any technical questions.
AlveoliX’s mission is to make organs-on-chips the new standard for preclinical decision-making and the leading alternative to animal experiments. With our technology we reproduce the microenvironment of human organs in an unprecedented way to gain more insight into human biology.
Booth: 65
ASPIS cluster is a joint collaboration of the H2020 funded projects ONTOX, PrecisionTox, RISK-HUNT3R and represents Europe’s €60M effort towards the sustainable, animal-free and reliable chemical risk assessment of tomorrow.
Booth: 31
Avantor®, a Fortune 500 company, is a leading global provider of mission-critical products and services to customers in the biopharma, healthcare, education, government, and advanced technologies and applied materials industries.
For the preclinical and clinical trial community, Avantor Services offers an experienced team of skilled associates that has a proven track record of excellence. We ensure that you have the products, processes and pain-point solutions you need – from discovery through delivery – to focus your valuable time on your research and patient outcomes.
Our services include custom kitting, clinical trial equipment and ancillary supply solutions and biorepository and archiving.
Avantor – we set science in motion to create a better world.
Booth: 4
Beijing Huironghe company founded in 2010, is a high-tech company specializing in the research and development, production, sales and technical services of toxicological experimental instruments, providing comprehensive toxicological experimental solutions and professional technical support to customers.
Booth: 62
Biobide is a Contract Research Organization with more than 18 years of experience offering Zebrafish alternative model in Toxicity and Efficacy screening assays as well as disease modelling to Pharmaceutical, Biotech, Chemical, Tobacco and Cosmetic companies.
All the know-how acquired during these years allows us to predict toxicities in a cost-time effective manner, such as acute toxicity, developmental toxicity, cardiotoxicity, hepatotoxicity, ototoxicity, neurotoxicity, immunotoxicity or ecotoxicity in discovery process.
We are experts developing fine tune studies based on our clients’ requirements: validation of diverse targets, models generation and toxicity/efficacy studies in different therapeutic areas (CNS, immune system, cancer, orphan diseases, etc.).
Booth: 60
BioClavis Ltd is a Glasgow-based personalised diagnostics spin-out of US-based BioSpyder Technologies. Leveraging the proprietary TempO-Seq® transcriptomic/genomic platform technology (developed by BioSpyder), BioClavis is capable of efficiently analysing large cohorts with customisable biomarker panels of tens to thousands of genes, quickly and inexpensively. TempO-Seq has critical usability features and controls, and does not require specialised instrumentation, making it ideal for expansion into the clinic. These strengths, in concert with centralised patient samples, clinical research partners, and economic decision making, allow accelerated content discovery, product development and adoption of a new generation of cost-disruptive precision medicine testing worldwide.
Booth: 14
BioIVT enables smarter science and accelerates medical breakthroughs by delivering high-quality personalized biospecimen solutions and research services to life science and diagnostic industries. Recognized as an industry leader, we specialize in control and disease state samples including human and animal tissues or preparations, cell and gene therapy products, blood, and other biofluids, as well as ADME contract research services from standalone bioanalytical support through tiered in vitro studies with submission-ready reports to customized consulting.
By combining our technical expertise, exceptional customer service, and unmatched access to biological specimens, BioIVT serves the research community as a trusted partner in ELEVATING SCIENCE®.
Booth: 21
Bioneeds is an OECD GLP-certified and USFDA audited pre-clinical CRO providing regulatory testing services for Agrochemicals, Industrial chemicals, Specialty chemicals, Pharmaceutical, Biopharma, Herbal / Nutraceutical, Medical Devices and other industries.
Booth: 67
BSL BIOSERVICE Scientific Laboratories Munich GmbH is an internationally active Contract Research Organization (CRO) and preferred partner of Eurofins, a world leader in analytical testing. Our laboratories are part of a global scientific network offering services from discovery and preclinical testing to market approval.
BSL BIOSERVICE offers a broad range of biological safety and activity testing services for BioPharmaceuticals, Chemicals, Medical Devices, Agrochemicals, and Food.
A high degree of customer orientation, high quality and flexibility are core values of our corporate philosophy. A highly experienced team of scientists guarantees acceptance by national and international authorities and supports customers from early research until finalization of pre-clinical studies.
BSL BIOSERVICE is accredited with DIN EN ISO 17025 for biocompatibility testing of medical devices and certified in accordance with Good Laboratory Practice (GLP).
In February 2014 BSL BIOSERVICE furthermore earned full accreditation from the Association for the Assessment and Accreditation of Laboratory Animal Care (AAALAC) International.
BSL BIOSERVICE was established in 1995 as spin-off of a small biotech company founded in 1984. In 2015 all in vitro Services of BSL BIOSERVICE have been integrated in Eurofins BioPharma Product Testing Munich GmbH. The in vivo safety testing services for small and large molecules, chemical substances and medical devices have remained with BSL BIOSERVICE Scientific Laboratories Munich GmbH.
Booth: 11
For over 70 years, Charles River has served the world’s industries by
- supporting 86% of novel FDA approved drugs in 2021
- helping 1000+ industrial chemicals reach the market
- assisting in the approval of 34+ agrochemical actives.
Our scientific experts leverage an expansive safety assessment portfolio, a range of laboratory support services, and global state-of-the-art facilities to produce the quality data you need to optimize your product development program – every step of the way.
Toxicology expertise includes general toxicology, immunotoxicology, genetic, ocular, neuro, developmental and reproductive toxicology (DART), and more.
Booth: 30
CN Bio’s aim is to transform the way human-relevant pre-clinical data is generated to improve drug discovery efficiency. Our PhysioMimix™ OOC range of microphysiological systems & services enable researchers to predict human liver responses to acute & chronic drug exposure in the presence or absence of disease using single- or multi-organ liver-on-a-chip models. By recreating human physiology in vitro, PhysioMimix OOC provides high-content, predictive data that translates between lab and clinic.
Booth: 64
We are experts in model development with a strong focus on assays for neurotoxicological hazard assessment. DNTOX is a German bioanalytical testing laboratory for animal-free screening of chemicals regarding their potential to disturb human brain development and cause developmental neurotoxicity (DNT). Our in vitro testing battery uses human cell models and enables artificial intelligence-based chemical screening with in-house developed software. We work according to the 3R principles and want to promote our new approach methodologies (NAMs) to reduce animal testing.
Booth: 37
Ellegaard Göttingen Minipigs is the breeder of Göttingen Minipigs founded on the idea of offering a well-defined non-rodent model with a high translational value. Göttingen Minipigs are bred in our AAALAC accredited barrier facility in Denmark focusing on our core values; Animal welfare, respect, collaboration and quality. We deliver animals to most of the world with dedicated partners supplying the markets in North America, Japan, Taiwan and South Korea. Furthermore, we provide animals with e.g. permanent catheters, VAP ports, or telemetry devices plus surgically or diet induced disease models; all in addition to the collaborative development of transgenic Göttingen Minipigs.
Booth: A6
EPISKIN, world leader in tissue engineering, offers Human Reconstructed Tissues to the global scientific community to support research and development activities in Safety and Efficacy.
We provide our worldwide clients RELIABLE AND RELEVANT IN VITRO TOOLS FOR SAFETY AND EFFICACY EVALUATION.
Based, we partner with cosmetical, pharmaceutical and chemical industries to develop relevant and reliable safety and efficacy tests. Our models are critical tools to speed up Research and Development phases and to shorten the time to market. Some screening tests are already referenced and validated as alternatives to animal use, and others are in the process of validation.
Booth: 71
European Research Biological Center (ERBC) articulates the technical, scientific and regulatory expertise, know-how and track record required for non-clinical studies of any type of drug candidate, from preclinical proof-of-concept to market.
Offering a comprehensive range of experimental capabilities, preclinical models, regulatory pre-IND package and consultancy services, ERBC allows drug discovery and chemical industry professionals to de-risk innovation and enhance R&D productivity.
With highly qualified teams in France and Italy, ERBC is offering a customer-centric approach while committed in improving all aspects of non-clinical study design and conduct, combining the 3Rs and considering animal well-being as a priority.
Booth: A3
esqLABS provides consulting and services for the development and utilization of PBP(T)K and QST modeling & simulation platforms utilizing OPEN-SOURCE software as value-generating, holistic modeling & simulation solutions to support our customers decision making process along the entire life cycle of pharmaceutical, chemical, or crop protection products.
Booth: 44
Eurofins BioPharma Product Testing (BPT) laboratories in the D-A-CH region can look back on up to 90 years of experience. We are part of the world’s largest network of GMP certified laboratories, which offers comprehensive laboratory services for (bio-)pharmaceutical and medical device companies.
In Germany, Austria and Switzerland, we are at your disposal at seven locations, in Birkenfeld, Hamburg, Homburg, Constance, Munich, Linz (AT), and Schoenenwerd (CH).
Our services help you bring safe human and veterinary medicines to market. In addition to the pharmaceutical industry, we work for customers from the medical device, chemical and cosmetics industries.
Booth: 70
We are the European Chemicals Agency, an agency of the EU. We implement the EU’s chemicals legislation to protect your health and the environment. Our work also contributes to a well-functioning internal market, innovation and the competitiveness of Europe’s chemicals industry.
Chemicals make modern life possible – everything is made from them. Better knowledge and regulation of harmful chemicals protects workers, consumers and the environment, makes recycling easier, and encourages industry to develop safer alternatives.
Booth: A9
European Publishing is an Open Access Publisher of 6 peer-reviewed journals (including the journal Public Health and Toxicology, a media partner of the EUROTOX 2023 conference).
Based in the Science and Technology Park of Crete, one of the main units of the Foundation of Research and Technology, European Publishing adheres to ICMJE and COPE guidelines, supports the THINK-CHECK-SUBMIT initiative and has been responsible for its official translation into two European languages. It is supported by the European Union Regional Development Fund, and it is also a proud member of OASPA, ALPSP and ELEVATE GREECE.
Booth: A10
The Danish Society for Toxicology and Pharmacology is honoured to organize EUROTOX 2024 in Copenhagen, the capital of Denmark.
The congress will take place from 8 to 11 September 2024. The congress theme “Combined efforts in quest of safer chemicals and medicines” reflects the congress programme including a variety of topics dealing with safety of drugs and environmental chemicals, new and emerging technologies, personalized medicine, human
health effects caused by exposure to chemicals as well as safety issues arising from climate changes.
On behalf of the Danish Society for Toxicology and Pharmacology, it is a great pleasure to welcome all participants to Copenhagen for EUROTOX 2024.
Booth: 1
FUJIFILM Cellular Dynamics, Inc. (FCDI) is a leading developer and supplier of human induced pluripotent stem cells (iPSCs) utilized in drug discovery and cell therapies. Leveraging its expertise in iPSC technologies to create iPSCs and differentiated tissue-specific cells, FCDI is committed to enhance the beauty of modern cell biology, drive innovations in discovery, and advance medicine. FCDI’s life science iCell® Products are highly pure, highly reproducible, and available in industrial quantities required for drug and cell therapy development. For more information, please visit: FujifilmCDI.com
Booth: 61
Galileo Research is a preclinical Contract Research Organization (CRO) that provides experience, knowledge, and skill required to take drugs, medical devices, food supplements and cosmetics on the market. We support discovery and development with a complete range of non-clinical studies. Our expertise in regulatory submissions and our knowledgeable strategic skills in planning non-clinical testing programmes are also provided to our Clients, to reduce attrition rate and speed up the process.
Booth: 42
GenoSafe is an analytical CRO providing testing services for the evaluation of quality, safety and efficacy of Gene and Cell therapies. GenoSafe brings its 20-year experience in the development, qualification and validation of analytical methods to perform preclinical biodistribution, shedding and immunogenicity studies according to Good Laboratory Practices – GLP.
GenoSafe will also provide its continuous support for clinical bioanalysis of patient samples (i.e immunogenicity, biodissemination and gene expression studies) as well as QC testing of your drug candidates.
Booth: 24
Genoskin is a TechBio company with research facilities in Toulouse, France, and Salem, MA, USA. Genoskin leverages immunology to de-risk the development of drugs, biologics and vaccines by providing early access to animal-free, first-in-human data prior to clinical trials.
Genoskin’s ex vivo study platforms contain natural, bio-stabilized and immunocompetent human skin from representative donor cohorts. They allow evaluating drug efficacy and toxicity for different routes of administration and include the world’s first platform to assess preclinical human response to subcutaneous or intradermal administration.
Our experts combine the vast data sets generated by its platforms with advanced analytical technologies, including next-generation transcriptomics, multiplexed proteomics and AI, to provide actionable study results and reduce the length, costs and risks of drug development.
Booth: A8
Gentronix is a predictive toxicology CRO delivering innovative services to the global pharmaceutical and chemical sectors. Our in vitro and in vivo GLP capabilities cover skin and ocular corrosion/irritation and skin sensitisation endpoints through to a full genetic toxicology range of GLP services.
Since 2021 Gentronix has been the sole global provider of the transgenic rodent Big Blue® model to support in vivo mutagenicity assessments under the OECD 488 guideline, with GLP OECD 488 contract services now available.
Booth: 54
ICCR-Rossdorf offers experimental toxicological expertise since more than 3 decades.
Our key area is investigations of the genotoxicity potency of pharmaceuticals, agrochemicals, cosmetics and chemicals. However, several additional disciplines of toxicology, mainly in vitro methods, are in our portfolio (e.g. skin/eye irritation and corrosion, cytotoxicity, sensitisation testing). For customers from the medical device industry we offer modified protocols using extracts in accordance to ISO 10993-1 (EN 17025 certified since 2011). Almost all toxicological studies are performed under GLP in accordance to OECD Guidelines.
In addition, batch release testing of pharmaceuticals under GMP has been performed for more than 10 years.
Booth: 18
At IDEXX BioAnalytics we’re dedicated to supporting your research needs by providing fast, accurate and reliable results— along with expert consultation you can access directly, for even greater insight. IDEXX BioAnalytics delivers comprehensive animal health monitoring, biological materials testing and preclinical services so you can test with confidence.
Booth: 25
ILSI Europe fosters collaboration among the best scientists from industry, academia and the public sector to provide evidence-based scientific solutions and to pave the way forward in nutrition, food safety, consumer trust and sustainability. To deliver science of the highest quality and integrity, scientists collaborate and share their unique expertise in expert groups, workshops, symposia and resulting publications. Whereas ILSI Europe’s activities are mainly funded by its member companies, academic experts involved in our activities contribute through their voluntary work. In addition, ILSI Europe receives funding from the European Union-funded projects they partner with and from projects initiated by Member States’ national authorities.
Booth: 13
ImmuONE is a biotechnology company that offers immune-competent models of the lung for use as an inhalation-based contract research organization. We provide outsourced projects for industries such as consumer products and pharma. Our unique and innovative approach aims to revolutionise the drug discovery process by reducing the cost and time associated with traditional in vivo and in vitro testing. Our goal is to provide high-quality, reliable, and cost-effective services to our clients while contributing to the advancement of science and medicine.
Booth: A1
Infinite Biotech is a spin-out of the Slovenian largest research institute, developing unique IN FINITE (in vitro – in silico) animal-free toxicity assessment technologies for prediction of several chronic diseases (alternatives to OECD TGs 412, 413 and 452), to identify hazardous triggers such as particulate-matter potentially inducing slowly evolving diseases such as chronic inflammation in lungs, aseptic bone-implant loosening and neurodegenerative diseases. We aim to help the industry to pre-screen novel advanced materials from early R&D stages for their long-term safety and replace possibly problematic materials with their safer alternatives, possibly far before they enter a mandatory animal-based study required by REACH. In addition, the same technology can be employed to cost- and time-efficiently identify any hazardous working place along any dusty production process.
Booth: 7
As an innovative and dynamic contract research organization (CRO) InnoSer supports the preclinical pipeline from its facilities in Belgium and the Netherlands. Founded in 2012, our in-depth expertise allows us to provide customized and streamlined early drug development options with well-characterized and near-patient research models. Our services are designed with personalized tailoring in mind, supported by innovative technical capabilities and are executed in close collaboration with our partners. Our current operations focus is within the later stages of drug-discovery and early preclinical research.
Booth: 54
Inotiv, Inc. is a leading contract research organization specializing in nonclinical and analytical drug discovery and development services. The Company focuses on developing innovative services supporting its clients’ discovery and development objectives for improved decision-making and accelerated goal attainment. The Company’s products focus on increasing efficiency, improving data, and reducing the cost of taking new drugs to market. Visit inotivco.com for more information.
Booth: 8
InSphero is the only 3D in vitro model company with the platform and expertise to modernize drug safety and drug efficacy testing in a way that empowers researchers to reach their full potential. Our innovative spheroid-based models allow for more effective, safe therapies to reach the clinic through truly superior robustness, reliability, reproducibility, and scalability. InSphero’s goal is to inspire the next generation of breakthrough therapies through customer devotion, commitment to innovation, and the model of excellence.
Booth: 49/50
Instem is a global provider of leading software solutions and scientific insight services that is helping clients to bring their life enhancing products to market faster, transforming the future for the benefit of everyone. We enable organizations in the life sciences to collect, report and submit high quality regulatory data more efficiently, while offering them the unique ability to generate new knowledge through the extraction and harmonization of actionable scientific information. Our intelligent solutions empower collaboration and life enhancing science.
Booth: 9
IIVS is a GLP-compliant Contract Research Organization focused on non-animal alternatives to toxicology and product safety testing. We assist companies and other institutions in the implementation of in vitro testing strategies that limit animal use. In addition, IIVS assists in the validation of New Approach Methodologies (NAMs) to traditional assays. Our services include assessments of: dermal and ocular irritation and corrosion, dermal sensitization, photosafety, genetic and respiratory toxicology. As a non-profit entity, our laboratory activities and contributions fund our Education and Outreach programs, providing extensive training and active involvement in the advocacy and promotion of non-animal methods worldwide.
Booth: 6
Intox is an OECD GLP certified preclinical safety assessment service provider with 25+ years expertise in conducting safety assessment studies for small and large molecules. The state-of-the-art facility is spread across 45,000 sq ft in Pune, India. Our scientific team of experts include board-certified toxicologists (DABTs), pathologists (ACVP and DIBTP), study directors, study personnel, veterinarians, analysts and QAU.
Over the years, we have conducted more than 15,000 GLP studies for a wide range of industries including pharmaceutical, bio-pharmaceutical, medical device, agrochemical, industrial chemical, neutraceutical /dietary supplements, cosmetics and others.
Booth: 22
Invitrolize offers innovative 3D alveolar in vitro models allowing to predict the hazard of respiratory sensitization and irritation. The company was created by researchers and scientists, and this is the reason why we maintain the same high quality standards in everything we do. Our products deliver the most reliable results because we only focus on one thing, data.
Booth: 41
JRF Global is a Non-Clinical Contract Research Organization, with our toxicity facilities at our headquarters near Vapi, Gujarat.
The principal services of JRF are dedicated to establishing efficacy and safety of your products using highly credible research capabilities in Product, Analytical & Residue Chemistry, Environmental fate & Metabolism, Mammalian Toxicology, Mutagenicity and Bio-analytical Chemistry under endorsement of our compliance with Good Laboratory Practices by the GLP Compliance Monitoring Authority of Government of India. Our animal facility is accredited by AAALAC, USA.
The professional experience exceeding 42 years and the expertise give JRF a competitive edge, establishing its highly valued international brand. The client list exceeds 800 companies.
The accreditation bestowed upon JRF are
- AAALAC
- GLP Monitoring Authority of Govt. of India and The Netherlands
Booth: 17
KaLy-Cell has been developing its expertise in liver-related ADME-toxicology, ex-vivo and particulary in-vitro with hepatocytes, for almost 20 years, helping in optimizing the discovery, development and approval of drugs, food additives, agrochemicals and nutraceuticals.
KaLy-Cell delivers unique information, mainly with hepatocytes, from animal and human origin, qualified in short- and long-term culture to best support evaluation of drug efficacy, xenobiotic safety, and to explain mode of actions and adverse reactions.
www.kaly-cell.com/why-kalycell/
Booth: 12
KREATiS is a unique organisation offering you in silico ecotoxicology, mammalian toxicology and physical chemistry predictions to screen the hazards of your substance or to complete your regulatory dossiers or boost your R&D in the most time and cost efficient way possible using:
- Our home-grown, high accuracy QSAR models in the form of iSafeRat® Platform
- A comprehensive choice of third-party software to fill the remaining datagaps that iSafeRat® does not cover
The combination of these will help you to fill your datagaps with the best in silico study predictions available, meeting the 5 OECD principles for the validation of QSARs and regulatory format requirements for a host of dossier submissions and updates notably for REACH and CPSR, ICH M7, Medical devices, but increasingly for aspects of Plant Protection Products and Biocides.
Booth: 47
Clear and confident healthcare decisions begin with questions. At Labcorp, we’re constantly pursuing answers. With unparalleled diagnostics and drug development capabilities, we accelerate innovation and provide insight to improve health and improve lives. Whether you’re a patient, provider, researcher or in the pharmaceutical industry, we’re here for you. Learn more at www.Labcorp.com or follow us on LinkedIn and Twitter @Labcorp.
Booth: 3
LGC provides a comprehensive portfolio of biologically relevant models, including patient-derived cancer organoids, reporter-labeled cells, and an unparalleled collection of cancer cell lines from the world’s largest biorepository, ATCC. LGC manufactures TRC’s uniquely large range of research chemicals, including bioactive molecules, SILs, modulators of angiogenesis and apoptosis, as well as biological targets such as protein kinase and cytokine receptors.
Booth: 26
Lhasa Limited is a not for profit organisation. At Lhasa, we are driven by our purpose; To enable informed decision making on chemical safety. In line with this purpose, we create cutting-edge software solutions, which have been solving real-world chemical safety assessment problems for almost 40 years. Our technology is designed by scientists, for scientists, in collaboration with industry stakeholders and regulators. We are committed to enabling scientists to make better predictions on the safety of drugs, chemicals and cosmetics by using existing data better and developing computer-aided reasoning and information systems for the advancement of science.
Booth: 28
LifeNet Health LifeSciences is a leader in all-human research solutions that accelerate discovery. Our commitment to honoring donors leads to unsurpassed quality and human-relevance, including the largest selection of comprehensively characterized liver cells and tissue. Our pioneering hepatic in vitro systems provide reliable options for alternative methods to animal testing. We also offer prospective biospecimen recovery, a range of toxicology services, and unparalleled scientific support.
Booth: A7
Locsense develops and supplies impedance spectrometers / TEER detectors for in-vitro cell cultures.
Booth: 38
Łukasiewicz – IPO is a leading research and development centre with more than 75 years of tradition which performs a wide variety of toxicological and ecotoxicological studies. We conduct studies for companies worldwide, cooperates with both domestic and foreign research units as well as actively participates in research projects. Our studies states a guarantee of quality, which is confirmed by GLP certificates and full AAALAC International accreditation. The aim of the studies mentioned above is to evaluate possible harmful effects of various chemical substances on human health, animals and the natural environment.
pszczyna.ipo.lukasiewicz.gov.pl
Booth: 58
MatTek is at the forefront of tissue engineering and is a world leader in the production of in vitro 3D reconstructed human tissue models for regulatory toxicology. Our skin, ocular, mucosal, and respiratory tissue models address toxicology and efficacy concerns throughout the cosmetics, chemical, pharmaceutical, and household product industries.
MatTek´s human cell-derived 3D tissue models provided impressive results in a number of international multi-laboratory validation studies. Our EpiDerm and EpiOcular models are validated by OECD as an alternative to animal testing.
MatTek’s 3D tissue models are successfully used worldwide by leading testing laboratories, educational institutions, and industrial corporations.
Booth: 19
MIMETAS is a global leader in disease modeling using Organ-on-a-Chip technologies. Founded in 2013 in Leiden, the Netherlands, MIMETAS strives to contribute to ground-breaking therapies with unique human disease biology, revealed by robust, screenable assays in their proprietary platform, the OrganoPlate®. MIMETAS believes that phenotypic tissue-and disease modeling is at the heart of 21st-century therapy development.
Booth: 55
Molecular Networks Altamira (mn-am.com) offers innovative solutions in computational toxicology and chemical safety assessment. The ChemTunes·ToxGPS® platform provides a unique combination of highly curated toxicity and safety databases containing a full-featured chemical, regulatory and toxicity data search and retrieval system and a knowledgebase that offers MoA-based predictions for toxicity endpoints of regulatory importance, TTC analysis, profiling tools to assess structural, biological, and physicochemical similarity of compounds, and a flexible workflow to perform consistent, reproducible, and transparent read-across. The toxicity prediction and read-across workflows employ a rigorous decision theory approach to provide weight of evidence-based outcomes.
Booth: 33
Welcome to MultiCASE, Inc. – Computational Toxicology Specialists –
For 25 years, MultiCASE has developed state of the art cheminformatics tools and computational toxicology software platforms for evaluating biological activity and toxicity potential for chemicals. Our software applications are used by regulatory agencies, pharmaceutical, chemical, and cosmetic companies worldwide. Consulting and licensing services are provided to fulfill REACH requirements or ICH M7 Step 2 compatible in silico evaluation for drug candidates, impurities, and reagents.
Whether you’re engaged in exploratory research or decision-making within the regulatory landscape, our goal is to create software tools to complement your decision making expertise throughout a risk assessment.
Booth: A5
Nagi Bioscience provides cutting-edge laboratory equipment to unlock the full potential of micro-organisms for high-content screening of drugs, chemicals and other substances. Under the motto of “in vivo testing at the in vitro scale”, Nagi Bioscience works for the transformation of biological testing standards by creating faster, more scalable, reproducible, and efficient ethical methods to boost innovation and efficiency in the pharmaceutical, chemical, and consumer goods’ industries.
Booth: 5
NUVISAN offers a fully integrated toxicity testing platform at our GLP-certified test facility in Germany following all international standards (OECD, ICH, REACH, JMAFF, FDA [&] EMA guidelines). With the customized solution, we assess the safety of your lead compounds in a comprehensive [&] efficient way by the combination of various in vivo, in vitro, or analytical investigational methods.
We fully embrace the 3Rs principle for humane animal care and are in compliance with high animal welfare standards (e.g. AAALAC accreditation) [&] animal welfare development program.
Booth: 2
PELOBIOTECH is competent for cells and offers the broadest portfolio of animal & human cells (e.g. hepatocytes) and media. We bring your research from bench to bedside. You get the whole variety of solutions from tissue dissociation to cryopreservation for research and clinical applications (GMP). Tissue Dissociation Enzymes; Defined & Xeno-free Media; Human & Animal Primary & Stem Cells from healthy & diseased donors; Tagged Cells; IPS & IPS derived Cells, Media, Reprogramming & Small Molecules; 2D/3D Cell Culture Systems.
Booth: 63
Penman Consulting is “the applied sciences company” supporting diverse industries with their global regulatory requirements. We combine our relevant experience and expertise with our product stewardship platform Active Steward™ (developed in-house) to provide a unique service including human health & environmental testing and read-across strategies, study monitoring, mechanistic toxicology, exposure & risk assessments and regulatory affairs tailored to your needs.
Booth: 68
Pepper is a public-private platform working at the European level, financially supported by the French “Programme of Investments for the Future” as well as by Pepper’s members (private and public organisations). Pepper is a non-profit association created within the French National Strategy for Endocrine Disruptors.
Pepper carries out and contributes financially to:
- the identification and documentation of mature methods meeting a need in terms of identification of EDs;
- the assessment of the transferability, repeatability and reproducibility of the method through ring testing;
- the support to method developers in forwarding their methods and the required scientific reports to international validation authorities
Booth: 35
PhoenixBio is a global leader in the development and distribution of high-quality human liver models. Our PXB-Mouse® is a humanized liver animal model and has a liver repopulated with up to 98% human hepatocytes. PXB-cells® are human hepatocytes freshly isolated from the PXB-mouse and are frequently applied for in vitro research.
PhoenixBio models accelerate pharmaceutical and chemical compound development due to their unique ability to deliver preclinical insights that are more predictive of human outcomes. Our models are applied in several research areas, including viral hepatitis (HCV, HBV, HBV/HDV), NASH/NAFLD, Gene Therapy & Editing, DMPK/Toxicology, and more!
Booth: 16
Porsolt provides in vitro assays, pathophysiological, models in multiples species and cell lines, customized procedures, and tailored solutions. We offer to support your drug development using high throughput screening, high content analysis, and high content histology platforms, drug formulation analysis and bioanalytical services. Our vast expertise covers the following areas: psychiatric and neurological disorders, cardiac and vascular diseases, oncology, pain, inflammation, gastrointestinal disorders, liver diseases, metabolic and eating disorders, respiratory diseases, dermatology, medical devices, and predictive toxicity of compounds.
Booth: 57
PRIMACYT offers one of the world’s most comprehensive portfolios of liver related products obtained from human and animal species like birds, fresh and seawater fish, rodents, and farm animals. We offer primary human and animal cells, liver subcellular fractions, ex vivo skin explants, blood derived cells, and consumables for applications in environmental toxicology, preclinical testing and product development in human and animal health. Products are manufactured in accordance with OECD test guidelines.
We have a validated technology platform to assay drug transporter activities in stably transfected HEK293-cells and primary hepatocytes. We are GLP certified and serve as a reference laboratory for the EU.
Booth: 48
RIFCON GmbH is an independent scientific consulting company offering the entire service portfolio as CRO and Consultancy regarding the evaluation and registration of chemicals and biopesticides with more than 20 years of experience.
Toxicology is one of the key subjects in the registration process. The team of highly skilled toxicologists at RIFCON is qualified in the assessment of acute and short-term effects, genotoxicity, carcinogenicity, reproductive toxicity as well as endocrine disrupting properties.
We offer services such as monitoring and assessing toxicological studies, providing in silico analysis (QSAR, profiling and read across) for evaluating relevance of impurities and metabolites and many more.
Get in touch via info@rifcon.de
Booth: 66
SaferWorldbyDesign is a solution-oriented, safety assessment platform supporting the design and testing of intelligent, safer products using new approach methods in toxicology and next generation risk assessment.
Booth: 52
Scantox is the leading Nordic preclinical GLP accredited CRO – Contract Research Organization.Based on decades of experience we are a trusted partner for in-vivo preclinical research services for the pharmaceutical and medical device industries. The Scantox services enable clients to progress their drug or device development based on consistent, high-quality solid data to the highest technical and scientific standards. Scantox is based in Denmark, with subsidiaries in Sweden.
Booth: 20
Scymaris Ltd is headquartered in Brixham, Devon UK. We offer high quality and cost-effective ecotoxicology, environmental fate, and analytical chemistry services to the global agrochemical, pharmaceutical, industrial chemicals & biocides industries. Our extensive state of the art laboratory facilities are equipped with controlled temperature rooms, freshwater and seawater treatment and processing capabilities, controlled air-flow and conditioning, security and back-up systems to provide a comprehensive suite of capabilities.
Booth: 36
SenzaGen aims to be a leader in in vitro science and testing, driving the transition from animal testing to methods better suited to reflect human biology. The Company provides state-of-the-art non-animal tests and tailored consulting services.
In 2022, SenzaGen’s GARDskin assay was adopted by OECD as part of Test Guideline 442E for in vitro skin sensitization. The scientific data published in the TG confirms the method’s high performance and demonstrated applicability for “difficult-to-test” chemicals such as complex mixtures, indirectly acting haptens, lipophilic compounds and metals, bringing new opportunities to the field of in vitro skin sensitization testing.
Booth: 45
Medicilon is an integrated contract research organization (CRO), providing comprehensive one-step new drug R&D for pharmaceutical enterprises and scientific research institutions around the world. Medicilon has built an integrated technical platform covering key technologies in drug discovery, pharmaceutical research, and preclinical research.
Booth: A2
The Slovenian Society of Toxicology is a voluntary association of citizens professionally engaged in toxicology. The purpose of the society is to maintain and promote knowledge of toxicology and the exchange of information from toxicological and related fields.
For the first time ever, the Slovenian Society of Toxicology has the honour of hosting a EUROTOX Congress.
Booth: 27
StageBio is a provider of GLP-compliant research, preclinical & clinical histology, pathology & more.
Booth: 10
Syngene International Ltd. is an integrated contract research, development and manufacturing services company serving the global pharma, biotech, nutrition, animal health, consumer goods and specialty chemical sectors.
Our 5200 plus qualified scientists have both the skills and the capability to deliver great science, ensure robust data management, IP security and quality manufacturing, at speed, to improve time-to-market and lower the cost of innovation.
With 2 Mn sq ft of specialist discovery, development and manufacturing facilities, Syngene offers dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife. We also work with biotech companies pursuing leading edge science, and MNCs including GSK and Merck KGaA.
Booth: 53
Since 2010, TissUse has shown proficient expertise in the functional coupling of various human in vitro organ models on our commercially available HUMIMIC Multi-Organ Chips. We focus on multi-organ -chip solutions, connecting different organ models in a circulation to emulate systemic in vitro organ-organ interaction. The technology has been successfully deployed by a wide range of partners and clients (e.g. Roche, Bayer, AstraZeneca).
Booth: 69
ToxMinds is a product safety and regulatory affairs firm with offices in Brussels and Bangalore. Our passion is the use of good science in regulatory processes. Our team is composed of experienced toxicology, environmental and regulatory specialists supported by motivated research analysts. The industry sectors we work for include chemicals, biocides, cosmetic & consumer products, and pharmaceuticals. We closely follow the developments in regulatory toxicology, particularly in predictive toxicology, new approach methodologies and risk assessment concepts and endocrine disruption. Our motivation is to apply emerging methodologies in risk assessment and regulatory processes to reduce animal testing as far as possible.
Booth: 32
Toxys is a global leading expert that develops and offers a broad spectrum of unique animal-free laboratory tests for the safety assessment of novel medicines, chemicals, cosmetics and food. We are experts in the fields of genotoxicity, developmental toxicology and mechanistic toxicity testing. We develop assays with the focus on understanding the mode-of-action of toxic compounds. Our ToxTracker® assay accurately identifies genotoxic compounds, ReproTracker® detects developmental toxicity and the ToxProfiler™ assay provides a broad toxicity profile of compounds. Toxys is internationally recognised for its scientific expertise, high quality results and responsiveness.
Booth: 15
UPM Biomedicals is the world’s first to produce high quality wood-based nanofibrillar cellulose (NFC) for life science and clinical applications in accordance with ISO 13485 medical device quality management system.
GrowDex® is a ready-to-use hydrogel for 3D cell culture without temperature control, mimicking the extracellular matrix supporting cell growth and differentiation. NFC is used in multiple applications from HTS drug screening, 3D cell culture, personalized medicine and 3D bioprinting to tissue engineering.
We are part of UPM Corporation that provides renewable solutions for various end uses. We employ 17,200 people worldwide and our annual sales are approximately EUR 11.7 billion.
Booth: 29
About VIMTA:
Founded in 1984 with headquarters in Hyderabad, India. Vimta Labs is a leading contract research and testing organization with 19 satellite labs across India with a wide and global span of services to support Pharmaceuticals, Food, Electronics, Health Care, and other industries. VIMTA has been supporting many national and overseas businesses for close to four decades for their third-party testing, research, and outsourcing needs.
Our service portfolio includes analytical, clinical, and preclinical services to life sciences industries; providing an integrated scientific, technical, and regulatory expertise to support all stages of drug development and manufacturing process for small & large molecules.
We have a track record of strict compliance to regulatory requirements (cGMP, GLP, GCP) & Standards (ISO 17025, ISO 15189, ISO 9001), and have undergone numerous audits successfully from regulatory agencies across the globe.
Booth: 39
VITROCELL® is specialised in the development of advanced in vitro exposure systems. VITROCELL® realizes turnkey installations for in vitro inhalation toxicology where gases, environmental atmospheres, nanoparticles and complex mixtures are analyzed on lung cells at the air/liquid interface.
The company offers relevant exposure technologies for continuous flow exposure, liquid aerosols using Cloud single droplet sedimentation as well as for small quantities of dry powders.
VITROCELL® in vitro Exposure Stations are designed for fully automated exposure of environmental pollutants to cells of the respiratory tract.
VITROCELL® Skin modules are specially designed for the exposure of tissue.
A complete set of dosimetry tools is an essential part of the product program.
The customers of VITROCELL Systems GmbH are leading research institutes, contract research organisations, regulatory authorities as well as the pharmaceutical and other industries throughout the world.
Booth: 56
vivoPharm Global is a preclinical CRO with focus on toxicology and pharmacology services offering screening IC50 determination IHC Flow Cytometry cell-based assays in vivo studies and GLP- compliant IND packages. vivoPharm`s facilities are in Melbourne VIC and Adelaide SA and representation in Munich Germany to support European customers. A high demand toward our employees regarding quality of work flexibility communication and reliability enables us to guarantee performance of projects according to highest industrial standards.
Booth: 23
As a global company with operations across Asia, Europe, and North America, WuXi AppTec provides a broad portfolio of R&D and manufacturing services that enable the pharmaceutical and healthcare industry around the world to advance discoveries and deliver groundbreaking treatments to patients. Through its unique business models, WuXi AppTec’s integrated, end-to-end services include chemistry drug CRDMO (Contract Research, Development and Manufacturing Organization), biology discovery, preclinical testing and clinical research services, and cell and gene therapies CTDMO (Contract Testing, Development and Manufacturing Organization), helping customers improve the productivity of advancing healthcare products through cost-effective and efficient solutions. WuXi AppTec’s open-access platform is enabling more than 5,950 customers from over 30 countries to improve the health of those in need – and to realize the vision that “every drug can be made and every disease can be treated.”