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PDA Webinar: Enhancing Flexibility and Compliance for ATMP Manufacturing Facilities

Jun 11, 2020
Eastern Standard Time | Online
  • Virtual
  • Conference
  • Online


Moderator: Peter J. Makowenskyj, MEng, Director of Sales Engineering, G-CON Manufacturing 

Currently, speed to market for Advanced Therapy Medicinal Products is critical due to lack of capacity in this emerging field. Often, facilities are being designed and built while process development is still underway. How can one maintain speed while also taking into account efficient use of capital or process safety?

This webinar will offer a deep dive into drug product manufacturing and facility design, explaining how one can truly enhance flexibility while also ensuring due diligence and adherence to regulations in the process design.

Following the presentations, get your questions answered during a live 30-minute Q&A session with the speakers.

This webinar is presented as part of the 2020 PDA Advanced Therapy Medicinal Products Month.


  • 11:00 a.m. – 11:30 a.m.
    Multi-Modal ATMP Facilities to Satisfy Growing Demand
    Allan Bream, CRB
    Emily L. Thompson, PE, Process Engineer, CRB

    11:30 a.m. – 12:00 p.m.
    Case Study: Realization of Fill/Finish Project for an Oncolytic Immunotherapy ATMP
    Laura R. Moody, PhD, Product Manager – Primary Packaging and Pharma Liquid Packaging, North America, Syntegon Pharma Technology

    12:00 p.m. – 12:30 p.m.
    Q&A with Speakers

Highlighted Speakers

Allan J. Bream
Allan J. Bream
Laura R. Moody
Laura R. Moody
Syntegon Pharma Technology
Emily L. Thompson
Emily L. Thompson

Registration Fees

Registration Type Price
Member $200
Non-member $200
Gov't/Health Auth./Academic $200

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