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Do Extractable Protocols Truly Help - An End User Perspective
Extractables and Leachables Testing Using a Quality Risk Management Approach
Regulatory Requirements Pertaining to Animal-Derived Materials
Identifying Appropriate-Quality Pharmaceutical Raw Materials in an Evolving Regulatory Environment
The Role of BPOG Extractables Data in the Effective Adoption of Single-Use Systems
Overview of the regulatory landscape for plastic devices in pharmaceutical manufacturing
Overcoming Quality and Regulatory Challenges of Implementing Single-Use Pharmaceutical Manufacturing
Bioprocessing Raw Materials: Risk Mitigation Strategies
BPOG Model Solvent Comparison for Extractables Testing for Single Use Systems Drug Process Manufacturing
Guideline on Elemental Impurities: Challenges and Approaches for Implementation
Risk Based Assessment of Sterilizing Grade Filters
Facilitate Risk Assessment for Excipients with Emprove® Documentation
Formalized Risk Assessment: Challenges and Best Practices
Excipient GMP: The Industry Journey from Guides to Standards
BIOSIMILARS - Impact of Variability in Manufacturing Process