Whitepapers , Solubility Enhancement , Drug Product

Poor Solubility as a Program-Level Risk: How to Make Better Formulation Decisions

25 September 2026
Overview

Poor solubility can create uncertainty across formulation strategy, CMC development, clinical interpretation, and future manufacturing plans. 

Poor solubility is one of the most common challenges in pharmaceutical development, yet the greatest risk often lies not in the molecule itself, but in making formulation decisions without sufficient evidence. 

This whitepaper explores how development teams can avoid costly reformulation, unnecessary complexity, and delays by preserving formulation options until human pharmacokinetic (PK) data support a clear path forward. 

Download our latest whitepaper to read what our experts suggest on how to reduce risk, preserve development flexibility, and select the right formulation pathway with confidence. 

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Date
25 September 2026
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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...

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Dr. Asma Patel

VP, Global Commercial and Scientific Consulting - Drug Product

Dr. Asma Patel is responsible for providing scientific and technical support to Quotient Sciences' business development group and ...

About Asma
Robert Cornog

Senior Director, Product Development

Robert Cornog has over 26 years of experience in product development and process design. Across a broad range of dosage forms and ...

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Brad Rowe

Senior Director, Integrated Development

Brad Rowe joined the organization in 2005 and is based from our Philadelphia, PA sites in Garnet Valley and Boothwyn. He joined QS...

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