Moving Drug Substance Off the Critical Path — Streamlined Strategies to Accelerate to First-in-Human & Beyond, Upcoming Webinar Hosted by Xtalks


Drug substance plays a major part in ensuring a drug program achieves its major milestones, keeps to budget and delivers on its corporate goals.

The need for accelerated drug development has become even greater, with added pressure on Contract Development and Manufacturing Organizations (CDMOs) to deliver customer’s programs in a timely, efficient and agile manner. In the pharmaceutical industry, time is not just money, it can impact the entire program; a program which has been through years of careful consideration, strategic discussions and planning to get medicines to patients in need.

Drug substance plays a major part in ensuring a drug program achieves its major milestones, keeps to budget and delivers on its corporate goals. As every molecule and development program is different, there is no single manufacturing solution. Understanding what strategy to move forward with, what processes and technologies are available and who to partner with is key in achieving clinical and commercial success.

In this webinar, the featured speaker will discuss the different routes that drug developers can take to synthesize and manufacture their drug substance and evaluate their pros and cons. He will share how integrated drug substance and drug product capabilities in the candidate selection stage can aid in selecting the best molecules to move forward with into drug substance and onward into drug product formulations for the clinic. He will also touch on the key technologies that can be employed to establish a robust, and commercially scalable synthetic process that can greatly improve efficiencies, and reduce overall development timelines.

Join this webinar as the speaker explores case studies to demonstrate how drug substance and drug product development plans can be accelerated through innovative science and expertise to get drug substance off the critical path.

Join Stephen McQuaker, Director, Drug Development Consulting, Quotient Sciences, for the live webinar on Wednesday, June 15, 2022, at 11:30am EDT (8:30am PDT).

For more information, or to register for this event, visit Moving Drug Substance Off the Critical Path — Streamlined Strategies to Accelerate to First-in-Human & Beyond.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year, thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

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