Translational Pharmaceutics®

Take control and unlock your molecule’s true potential with integrated drug development expertise.

Accelerate molecules through development by integrating traditionally siloed services.

What is Quotient Sciences Translational Pharmaceutics®?

The Quotient Sciences Translational Pharmaceutics® platform is an integrated approach to drug development that combines formulation development, drug product manufacturing, and clinical testing into a single, seamless program. 

Translational Pharmaceutics® defines the interconnected relationship between drug product design, supply and clinical testing, saving you up to 12 months on early development timelines and reaching key milestones more efficiently.

  • Redefines Drug Development

For nearly two decades and more than 500 drug programs, we’ve pioneered the integration of CRDMO services. We merge operational efficiencies, scientific rigor, and clinical insights into a single program of work, delivered under a single project manager and organization.

  • Uses Efficiency to Save Time

Close integration between drug product manufacturing and clinical testing enables better decision-making while reducing time and waste. Our approach lets us manufacture and release drug products in less than seven days, then test and optimize in our clinics.

  • Applies Science-Led Insight

We've developed, tested, and manufactured a range of drug product formulations, both simple and complex. Our expertise across different dosage forms and therapeutics lets us anticipate and overcome challenges to create a personalized path for your molecule.

In control, on course and always one step ahead—no matter your development phase.

Quotient Sciences is an integrated CRDMO partner that puts you in control of your drug program, with trusted insight you need to navigate the complexity of early development.

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How does Translational Pharmaceutics work?
What benefits does Translational Pharmaceutics® offer?

Measurable, Trusted Results

Benefits of Translational Pharmaceutics
 

Streamlines & simplifies

vendor management & supply chain

Benefits of Translational Pharmaceutics
 

Better decisions

based on emerging human clinical data

Benefits of Translational Pharmaceutics
 

Timeline acceleration

by 12 months or more

Benefits of Translational Pharmaceutics
 

Cost savings

in R&D spend

 

Benefits of Translational Pharmaceutics
 

Provides flexibility

to adjust formulation composition within a study

Benefits of Translational Pharmaceutics
 

Conserves API

for high-value drug substance

How does Translational Pharmaceutics® disrupt drug development?
John McDermott, VP of Scientific Consulting, explains how Translational Pharmaceutics® helps remove drug development silos.
How is Translational Pharmaceutics® used?

Translational Pharmaceutics® helps you develop your drug—from first-in-human studies to managing your ongoing product lifecycle

  • Translational Pharmaceutics® for accelerating first-in-human, Phase I clinical testing 

    Reach a pivotal milestone with our phase-specific drug product to test the safety and tolerability of your drug. When Translational Pharmaceutics® is applied for your first-in-human clinical trials, you can accelerate to the clinic and see critical data faster to help inform development decisions downstream.
  • Translational Pharmaceutics® for drug product optimization in Phase Ib/IIa clinical studies

    We enable rapid formulation and optimization with clinical testing—simplifying reformulation after Phase I and beyond to manage product lifecycle, ensure continued innovation, and meet trial success. This is our RapidFACT® approach, an application of Translational Pharmaceutics®.
  • Translational Pharmaceutics® for more efficient, integrated human ADME studies

    Whether conducting human ADME for New Drug Applications (NDA) or running in parallel with Phase II Proof of Concept (POC) studies, our Synthesis-to-Clinic® integrated ADME studies are enabled by applying Translational Pharmaceutics®.
How does Translational Pharmaceutics® enable drug product optimization?
A novel, more efficient approach to drug development: Quotient Sciences Translational Pharmaceutics® integrates formulation optimization with on-demand clinical testing.
What do companies say about using Translational Pharmaceutics®?

Insight from our customers about the advantages of Translational Pharmaceutics®

Meet Quotient Sciences Translational Pharmaceutics® Experts

Dr. Andrew Lewis

Chief Scientific Officer

Dr. Andrew (Andy) Lewis is the Chief Scientific Officer at Quotient Sciences. As the leader of Quotient Sciences' scientific teams...

About Andrew
John McDermott

VP, Scientific Consulting

John McDermott leads Quotient Sciences' global drug development consulting, research fellows, modeling & simulation, and clien...

About John
Dr. Vanessa Zann

VP, Scientific Consulting, Translational Pharmaceutics & Clinical Pharmacology - USA

Dr. Vanessa Zann has over twenty-five years industry experience providing expert biopharmaceutic support to drug discovery, early ...

About Vanessa
Dr. Andrew Parker

Executive Drug Development Consultant

Dr. Andrew Parker has over two decades of experience in the pharmaceutical industry, spanning from preclinical development, throug...

About Andrew
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