2011 PDA Visual Inspection Forum Session Recordings

Web Code: VIF-P1-11
Member /Non Member Price: $199

Registration includes:

  • Recordings of all seven sessions from the Forum
  • PDF handouts of every presentation
  • Unlimited access to all session recordings for 60 days

Recording Overview

Visual inspection continues to be an important element of the manufacturing process and the quality assurance of injectable products. This interactive forum will closely examine the latest developments, preparation and use of inspection standards and practical aspects of manual and automated methods along with the regulatory and compendial requirements that govern them.
If you missed the 2011 Visual Inspection Forum, you now have the opportunity to listen to the conference recordings. 

Target Audience

If you are a decision-maker at mid-level or senior level, or a professional working at site or corporate level in the following areas these recordings will be beneficial to you:

Pharmaceutical/Biopharmaceutical Manufacturers
Engineering | Manufacturing | Packaging | Process Development | Quality | Technical Services | Validation

Pharmaceutical/Biopharmaceutical Developers

Clinical Supplies | Parenteral Development | Process Development Inspection Equipment Suppliers Applications Development | Machine Design | Sales

Recorded Sessions and Presenters

Medical and Regulatory Concerns with Particulate Matter
John Ayres, MD, Senior Director, Global Patient Safety, Eli Lilly and Company
Stephen Langille¬ł PhD, Senior Microbiology Reviewer, CDER, FDA
John G. Shabushnig, PhD, Senior Manager, Quality Systems and Technical Services, Pfizer

Special Considerations for the Inspection of Biotheraputics
Stephan Krause, PhD, Principle Scientist, MedImmune
Shawn Cao, PhD, Process and Product Development, Amgen, Inc
               
Supplier Quality and Component Defects
Roger Asselta, Vice President, Genesis Packaging Technologies
Ryan L. Smith, PhD, Scientist, Amgen, Inc

Case Studies
Akshay Kamdar, Associate Senior Consultant Engineer, Eli Lilly and Company
Romain Veillon, Vision Technology, GSK Biologicals
Bradley M. Rank, Senior Process Development Engineer, Bayer Healthcare Pharmaceuticals

Good Practices in Manual Inspection
Roy Cherris, Managing Partner, Bridge Associates International
James Melchore, Principal Consultant, Melchore Consulting
Dan Berdovich, Manager, Quality Assurance/Regulatory Affairs, Micro Measurement Laboratories, Inc

Good Practices in Automated Inspection
Deborah Shnek, PhD, Director, Process Development, Amgen, Inc
Rick Watson, Process Engineer, Merck and Company
Ryan Basdeo, Technical Service Engineer, Eisai Machinery USA Inc.
Effie Manziaris, Project Manager, Sanofi Pasteur Ltd.

Case Studies - Emerging Inspection Technologies
Heino Prinz, PhD, Head of Research and Development, Wilco AG
Maurice Murphy, Project Engineer, Amgen, Inc
Joseph Frantz, PhD, Senior Director, Pharmaceutical Technology, Sanofi Pasteur

Registration contact

Jason E. Brown
Senior Programs Manager
Tel: +1 (301) 656-5900 ext. 131
Fax: +1 (301) 986-1093
Email: brown@pda.org

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