Pre-Clinical Phase | Thermo Fisher Scientific

Prepare your vision

Proceed with confidence in this critical step with API and formulation development, IND enabling support, pre-clinical PK/PD, and other analytical analyses to determine if a drug candidate is safe before a human trial.

Research: Help Reduce Risk and Stay on Track

Design and execute studies with confidence using integrated CRO support that helps improve data quality, reduce delays, and keep your program on track.

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Testing: Help Generate Reliable PK/PD and Safety Data

Get the analytical insights you need to determine if your drug candidate is ready for human trials.

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IND: How to Move Your Therapy Forward

Align development, testing, and regulatory planning to reduce delays and accelerate your path to first-in-human studies.

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Gain access to robust lab support, tailored study design, regulatory consulting, epidemiology research and more, including:

A wide variety of bioanalytical laboratory capabilities
Preclinical dosage, toxicology, PK/PD and safety testing
Pre-IND/IND support

FDA or EMA filing support and representation
Clinical trial development, design, and methodology
CMC consulting for all types of pharmaceutical products

Pre-clinical resources

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Proceed with conﬁdence as you test and optimize your lead candidate to prepare for the clinical trial phase. Whether you’re preparing study data for IND ﬁling or developing a CMC strategy, browse solutions-driven resources to simplify—and help accelerate—your work.