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Whether your question is associated with optimizing your formulation or manufacturing process, or planning your clinical pharmacology study, we are here to help. 

Our experts have insight into a variety of topics, including:

  • Using real-time clinical data to make better formulation decisions
  • Ensuring maximum flexibility in clinical manufacturing and batch sizes
  • Meeting clinical trial program needs while reducing cost and waste
  • Selecting the best formulation technology for poorly soluble molecules
  • Transitioning between drug substance and drug product manufacturing
  • Minimizing chemistry costs and moving drug substance supply off the critical path

Learn more about our experience and ask our team a question today.

Meet our team

Dr. Stuart Mair from Quotient Sciences

Dr. Stuart Mair
Global Vice President, Medical, Early Development

About Stuart

Dr. Andrew Lewis from Quotient Sciences

Dr. Andrew Lewis
Vice President, Pharmaceutical Sciences

About Andrew

Mr. Nazim Kanji from Quotient Sciences

Mr. Nazim Kanji
Executive Director, Pediatric Services

About Nazim

Dr. Asma Patel from Quotient Sciences

Dr. Asma Patel
Vice President, Integrated Development Services

About Asma

Dr. Vanessa Zann from Quotient Sciences

Dr. Vanessa Zann
Senior Drug Development Consultant

About Vanessa

Mr. Iain Shaw from Quotient Sciences

Mr. Iain Shaw
Senior Director, 14-C Enabled Drug Development

About Iain

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