PDA Webinar: Enhancing Flexibility and Compliance for ATMP Manufacturing Facilities

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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.

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Standard Pricing

Standard Member Price

$200

GovernmentMember Only

$200

Health AuthorityMember Only

$200

AcademicMember Only

$200

Non-Member

$200

See Qualifying Criteria for Member Types.

Day 1

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
Agenda is subject to change.

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