Altasciences is a forward-thinking CRO offering a flexible approach to preclinical and clinical pharmacology studies, including formulation, manufacturing, and analytical services. Altasciences’ integrated, full-service solutions include preclinical safety testing, clinical pharmacology, and proof of concept, bioanalysis, program management, medical writing, biostatistics, and data management. Altasciences helps sponsors get better drugs to the people who need them, faster.
ATCC knows that worthwhile science takes time, especially in the pre-clinical toxicology stages of drug development. It is critical that the standards and assay systems used in toxicological testing are reliable and authenticated. We can help streamline your research by providing the most authenticated, advanced, and functional models available. Let ATCC revolutionize and accelerate your toxicology studies in every phase of the research and testing process.
Battelle is the world's largest, independent research and development organization, providing a full array of GLP-compliant, nonclinical services and efficacy testing of drugs, vaccines and biologics to pharmaceutical, biotech, agrochemical companies and government agencies. We are a pioneer in the field of inhalation technology, safety pharmacology, and toxicology, and provide critical therapies and solutions to improve healthcare worldwide.
Your study matters. Get the attention you deserve.
Certara optimizes R&D productivity, commercial value and patient outcomes through its unique portfolio of model-informed drug development, regulatory science, and market access solutions. In fact, 90+% of all novel drugs approved by the US FDA in the past six years were supported by Certara software or services. Its clients include 1,600 global biopharmaceutical companies, leading academic institutions, and key regulatory agencies across 60 countries. For more information, visit www.certara.com.
Can your research continue in times of crisis? Simply, yes. With a global network, extensive capabilities, and strategic advisory services, Charles River is committed to advancing your therapies and chemicals to regulatory approval. From specialized studies to full program support, you’ll find unique solutions in our proven portfolio of discovery, safety, and analytical services. Trust us for the decision-driving data and insight you need to make uninterrupted progress toward your goals.
Discover more about Covance’s deep scientific expertise within toxicology and across drug development and chemical testing. Learn about solutions such as Early Phase Development Solutions, SEND, Biologics, Immunotoxicology, and ecotoxicology. Covance is the drug development business of Laboratory Corporation of America® Holdings (LabCorp®) (NYSE:LH), the world’s leading healthcare diagnostics company. To learn more about Covance, visit www.covance.com.
Place your programs with Experimur and experience the superiority of a team skilled with decades of experience, top quality and unmatched service. Experimur’s expertise spans the full spectrum of preclinical studies, including General Toxicology (sub-chronic, chronic, carcinogenicity), Specialized Toxicology (Juvenile Toxicity, Developmental/Reproductive Toxicology, including Segment I, II & III, Multi-generation studies, and Sperm Morphology/Vaginal Cytology), Neuro- (Motor Activity, Functional Observational Battery, Learning and Memory Paradigms, Startle Reflex), Cardiovascular and Respiratory-Safety Pharmacology, as well as expertise in Infant Nutritional studies. We look forward to partnering with you.
Instem is a global provider of leading software solutions and services that help clients bring their life enhancing products to market faster. We enable clients to more efficiently collect, analyze, report and submit high quality regulatory data while generating actionable insights.
Around the world, Instem solutions are meeting the rapidly expanding needs of life science and healthcare organizations for data-driven decision making, leading to safer, more effective products.
ITR Canada (Bozo & ITR Group)
Located in Canada and Japan, ITR Group’s GLP-compliant safety testing services can support your next product registration effort in any global market. We perform studies in general toxicology, infusion, inhalation, safety pharmacology, immunology, DART, genetic toxicology lab support services include analytical, bioanalytical, ligand binding (PK, PD and biomarkers) assays, and flow cytometry.
Work with us and discover how pleasant and productive a customer centric philosophy can be.
Lhasa Limited is a pioneer in developing high quality software that delivers scientifically robust and trusted results. With knowledge of toxicology, metabolism and degradation chemistry, Lhasa draws upon over 35 years of experience to create state-of-the-art in silico prediction and database systems for use in chemical risk assessment. All science is developed in-house by Lhasa’s scientists, providing users with the opportunity to discuss queries directly with Lhasa expert scientist.
Risk Assessment Recording: Building
Secondary Pharmacology Models
MilliporeSigma, the life science business of Merck KGaA, Darmstadt, Germany provides specialized BioReliance® assay services for all industries, focusing on broad Genetic Toxicology for both GLP regulatory and non-GLP predictive screening services.
For over 30 years, Miltenyi Biotec has played a leading role in the design, development, and manufacture of products that advance biomedical research. Discover how our innovative technologies enable toxicology researchers to characterize and understand cellular functions. Click on the links below to learn more about:
- Tissue dissociation
- Magnetic bead-based cell isolation
- Flow cytometric analysis and sorting
- Fluorescent and non-fluorescent antibodies
- Growth media and cytokines
Promega Corporation designs and manufactures: cell-based assays that deliver more biologically relevant data for basic research, drug discovery, and screening applications including mechanistic toxicity, ADME, biologics bioassays, reporter technologies for cell signaling to protein interactions; novel protein function and analysis systems; manual to automated nucleic acid purification for research, biobanking and clinical applications; with custom assay design services and GMP capability.
StageBio is a leading provider of preclinical necropsy, histology, pathology, and specimen archiving services for the biopharmaceutical, medical device and contract research industries. With seven state-of-the-art, GLP-compliant facilities and a team of board-certified veterinary pathologists and laboratory technicians, StageBio has a well-earned reputation for quality, scientific integrity, and client satisfaction.
WuXi AppTec is a leading global pharmaceutical and medical device open-access capability and technology platform company with global operations. As an innovation driven and customer focused company, WuXi AppTec provides a broad and integrated portfolio of services to help our worldwide customers and partners shorten the discovery and development time and lower the cost of drug and medical device R&D through cost effective and efficient solutions.