PQRI Workshop: Co-processed Excipients to Enhance Medicinal Product Development and Continuous Manufacturing

PQRI Workshop:  Co-processed Excipients to Enhance Medicinal Product Development and Continuous Manufacturing

SAVE THE DATES!

A hybrid event – April 14-15, 2027

PQRI is organizing a 1-1.5-day PQRI Workshop that will bring together leaders and subject matter experts (SMEs) from regulatory agencies, industry, and academia to discuss the various issues and
views on Co-processed Excipients (CPEs) and what is needed to encourage the use of CPEs to enhance innovation in pharmaceutical development.

This workshop aims to facilitate interaction among stakeholders and will address the following topics

• • • What are CPEs and how are they made and controlled?
    • Technology, Manufacturing, and Formulation Benefits of CPEs
    • Safety Assessment of CPEs
    • Regulatory Considerations and Challenges
    • Marketing and Supply Chain Concerns

The Workshop will include small group discussions (“breakout sessions”) moderated by SMEs that will further explore the above topics.

PQRI encourages anyone who is interested in CPEs use in product development to register for this  workshop and join the in-depth discussions surrounding the technical benefits and regulatory hurdles that exist for CPEs and possible concepts for reducing the regulatory burden related to CPEs use in medicinal product development and continuous manufacturing.

Workshop Location
USP
12601 Twinbrook Parkway
Rockville MD 20852

Workshop Materials
A Workshop Save the Date flyer is available to down load here.  Please share with interested colleagues.

Questions
Please contact the PQRI Secretariat if you have any questions at +1(202) 230-5607 or email.