Translational Pharmaceutics®

Take control and deliver against your molecule’s true potential with an integrated approach to drug development—an innovative platform proven to shorten development timelines by 12 months or more.

Accelerate molecules through development by integrating traditionally siloed services.


The Quotient Sciences Translational Pharmaceutics® platform is a disruptive approach to drug development that helps you forge your own path to success and optimize every step by redefining the complementary, interconnected relationship between drug product design, supply and clinical testing. 

Translational Pharmaceutics® integrates activities and adapts solutions to help you reach key milestones as quickly and efficiently as possible.

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How does Translational Pharmaceutics work?
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Redefining Drug Development

Over 17 years and 500+ programs, we’ve pioneered the integration of CRO and CDMO solutions. We merge operational efficiencies, scientific rigor, and clinical insights into a single program of work that is delivered under a single project manager and organization.

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Enabling Acceleration

We bypass drug-development silos. Our comprehensive approach to formulation development, on-demand GMP manufacturing, and clinical testing leverages actionable data to empower successful outcomes—manufacturing and releasing drug products in less than seven days and reducing overall development timelines by 9-12 months on average.

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Integrating Efficiency

Close integration between drug product manufacturing and clinical testing enables better decision-making while reducing time and waste. Our phase-appropriate expertise anticipates and overcomes challenges to create a personalized path for your molecule. 

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

Benefits of integrated drug development with Translational Pharmaceutics®

See how Quotient Sciences enables a faster, integrated approach to drug development.

Benefits of Translational Pharmaceutics
 

Streamlines & simplifies

vendor management & supply chain

Benefits of Translational Pharmaceutics
 

Provides flexibility

to adjust formulation composition within a study

Benefits of Translational Pharmaceutics
 

Better decisions

based on emerging human clinical data

Benefits of Translational Pharmaceutics
 

Cost savings

in R&D spend

 

Benefits of Translational Pharmaceutics
 

Timeline acceleration

by 12 months or more

Benefits of Translational Pharmaceutics
 

Conserves API

for high-value drug substance

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

Translational Pharmaceutics® helps you develop your drug—from first in human (FIH) studies to managing your ongoing product lifecycle. Learn more about the unique applications of the Quotient Sciences Translational Pharmaceutics® platform.

  • 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?
Learn how Quotient Sciences can integrate formulation optimization with on-demand clinical testing using RapidFACT®, an application of Translational Pharmaceutics®.

By the numbers

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Trusted for over 17 years

as a proven method to integrate drug development and streamline process steps.

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100+ customers

globally have used the Translational Pharmaceutics® platform.

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More than 500 programs

completed in therapy areas including oncology, neurology (CNS), and pediatrics.

What our customers say about Translational Pharmaceutics®

Meet Quotient Sciences Translational Pharmaceutics® Experts

With decades of industry and drug development knowledge, meet some of our team members who can help you navigate questions about the integration of drug product manufacturing with clinical testing and realize the benefits of the Translational Pharmaceutics® platform for your next drug program.

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

Vice President, Scientific Consulting

John McDermott is Vice President of Scientific Consulting at Quotient Sciences. John leads Quotient Sciences' global drug developm...

About John
Dr. Vanessa Zann

VP Scientific Consulting, TP-CP USA

Dr. Vanessa Zann is an VP Scientific Consulting, TP-CP USA at Quotient Sciences, with over twenty-five years industry experience p...

About Vanessa
Dr. Andrew Parker

Senior 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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