Quotient Sciences Conducts Integrated Translational Pharmaceutics® Program in U.S. With Druggability Technologies

Translational Pharmaceutics Seminar Series - October 2018

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Title: Translational Pharmaceutics and the Benefits of Real-Time Adaptive Manufacturing

Many pharma companies are seeking new ways of making drug development more efficient and cost-effective. This has led to an increase in the outsourcing of development activities to contract research partners who focus solely on disciplines such as clinical testing, formulation development and manufacturing. This in turn has created a siloed approach to drug development where there is a distinct lack of communication between the multiple vendors working on a particular drug molecule. 

This seminar series explains the benefits of Translational Pharmaceutics, a unique approach which integrates formulation development, real-time adaptive manufacturing and clinical research. The seminar will illustrate how, by breaking down the siloes and integrating horizontally, we can operate with more flexibility in the early phases of drug development, shortening timelines and reducing costs.

In addition, it will describe a different approach to drug product manufacturing, called “real-time adaptive manufacturing” and how it can help adapt to clinical trial requirements quickly and manufacture on-demand the precise drug product required. The seminar will describe ways of maximizing flexibility around batch size, scale and product stability, whilst being truly responsive or “on demand” to the clinical trial requirements and the timing of product supply to any selected site, in response to emerging clinical data, or patient recruitment.

Key learning objectives

  • Discover how an integrated approach enables a quick transition of molecules from first-in-human to POC;
  • Understand how drug product formulations and doses can be adjusted and manufactured "real-time", often in response to emerging human data;
  • Learn how to save valuable API, through significant reductions in the amount of drug product manufactured;
  • Discover how to adapt to clinical trial requirements quickly and manufacture only the product your patients need;
  • Hear how this integrated approach can accelerate your drug development timeline.


San Diego, CA - Wednesday, October 17th, 2018     Learn more 

San Francisco, CA - Thursday, October 18th, 2018   Learn more 

Cambridge, MA - Wednesday, October 24th, 2018   Learn more

Drug product development

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