Which analytical methods are used to evaluate each type of degradation
The impact of product degradation on potency and safety
The evaluations of stability trends (or the lack thereof)
Design and execution of forced degradation studies during analytical method development
Who should Attend
Stability coordinators
Quality control managers
Stability department personnel
Laboratory directors
R&D laboratory supervisors and management
R&D laboratory personnel
Protein formulation group personnel and management
QC laboratory personnel and management
Regulatory affairs management
Regulatory affairs personnel
Past Events
Design and Execution of Stability Studies for Biologics 2016 - 19 Oct 2016, Webinar (62915)
Important
Please, check "Design and Execution of Stability Studies for Biologics" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical laboratories, Pharma
