FDA`s Update on Elemental Impurities According to the new ICH Q3D and USP 232/233 Guidelines - Are you ready? 2016
28 Sep 2016
Webinar
Description
Topics
Overview of Guidance Documents: FDA, ICH Q3D, USP 232/233
Elemental Impurities: The case for Change
Risk Assessment
Scope of the guidances
Controls and Documentation
FDA Recommendations
What you should be doing now
Analytical Procedures and Validation
Who should Attend
Regulatory Affairs personnel
Pharmaceutical R&D and QC chemists and their managers
Individuals at Contract Manufacturing and Contract Laboratory facilities
Past Events
FDA`s Update on Elemental Impurities According to the new ICH Q3D and USP 232/233 Guidelines - Are you ready? 2016 - 28 Sep 2016, Webinar (62365)
Important
Please, check "FDA`s Update on Elemental Impurities According to the new ICH Q3D and USP 232/233 Guidelines - Are you ready?" official website for possible changes, before making any traveling arrangements
