Stability Studies for Vaccine Products - Webinar By ComplianceOnline (Biotech Training)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Sep 12, 2012 End Date/Time: Sep 12, 2012
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Why Should You Attend:

This course will provide an overview of the Stability studies required for registration of Vaccines.

The Stability Program for vaccines is similar to but has significant differences from a stability studies for Biologic Products. This webinar addresses overall requirements for a vaccine stability study, contrasting it with the requirements for Biologics and small molecule products.

Areas Covered in the Seminar:

- Overview of the WHO requirements for vaccine Stability studies.
- What are the requirement for stability studies on Intermediates?
- What are the requirement for studies after product approval?
- What are the list of methods appropriate for a vaccine stability study?
- What is the concept of Cumulative Age?
Who will Benefit:

- Stability department personnel
- R&D Laboratory personnel
- R&D Laboratory Supervisors and Management
- QC Laboratory personnel and management
Protein Formulation Group personnel and Management.
- Regulatory Affairs personnel.
- Regulatory Affairs Management.
- QC Laboratory personnel and management.


Online Event
2600 E. Bayshore Road
Palo Alto
United States