Sterile Products Processing Update

Session 406
Technology Track

Aseptic processing technologies and the applicable regulatory requirements are constantly evolving. This is an excellent opportunity to learn how different users are handling and managing this change.

Session Description

Aseptic processing technologies and the applicable regulatory requirements are constantly evolving. Learn how different users are handling and managing this change.

At the conclusion of this session, participants will be able to:

Understand how technologies are being applied
Participate in panel discussions with people from industry
Understand changes/application of regulatory requirements
Network with colleagues and other professionals
Evaluate applications of technologies

Leaders

Speakers

Jeff Campie, USA
Richard Forsyth, Senior Consultant, Hyde Engineering + Consulting, USA
Nigel Hamilton, Global Quality, Strategy and Process Excellence, Sanofi Aventis, United Kingdom
Aisling Horan, Validation Scientist, Alkermes Plc, Ireland
Edwin Melendez, Principle Consultant, Parexel, USA
Mark O'Reilly, Director Engineering, Alkermes Pharma Ireland Ltd, Ireland
Kimberly Ray, A. Director Project Mgmt, Oso Biopharmaceuticals Mfg LLC, USA
Julian Wilkins, Vice President, PharmaConsult US Inc, USA
Paul Wreglesworth, Independent Consultant, United Kingdom

Who Should Attend

Manufacturing/Operations
Service Providers
Suppliers
Regulators

Communities of Practice Members that will Benefit

API
Biotechnology
Containment
HVAC
Operations Management
Oral Solid Dosage
Packaging
Project Management
Sterile Products Processing

More information on ISPE's Communities of Practice