Translational Pharmaceutics® for first in human studies

Reach a pivotal clinical milestone with our phase-specific approaches to test the safety and tolerability of your drug.
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Minimize upfront costs

related to chemistry, manufacturing, and controls (CMC)

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Increase precision

in the formulations that are developed and tested, keeping you in control of your molecule's development

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Reduce time

to first-in-human studies, so you can achieve the data you need and stay on-course to proof-of-concept

How is Translational Pharmaceutics® applied to drug development?

How to use Translational Pharmaceutics® to advance your next early development program

Beyond optimizing drug products, see how else Translational Pharmaceutics® can be applied to drug programs in these applications.

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How does Translational Pharmaceutics work?
  • Translational Pharmaceutics® for accelerating first-in-human, Phase I testing 

    Reach a pivotal milestone with our phase-specific drug product to test the safety and tolerability of your drug.
  • AI-enhanced formulation development within Translational Pharmaceutics®

Discover our new proprietary AI solution, combining Quotient Sciences intelligence with the power of AI, to achieve formulation decisions up to 50% faster.

 

  • Translational Pharmaceutics® for drug product optimization in Phase Ib/IIa studies

    Simplify reformulation after Phase I and beyond to manage product lifecycle, ensure continued innovation, and meet trial success. 
  • Translational Pharmaceutics® for more efficient, integrated human ADME studies

    Whether for New Drug Applications (NDA) or in parallel with Phase II / proof-of-concept studies, we integrate services to ensure better ADME study outcomes.
Now available: AI-enhanced formulation development within Translational Pharmaceutics®
Discover our new proprietary AI solution, combining Quotient Sciences intelligence with the power of AI, to achieve formulation decisions up to 50% faster.