Supplier Qualification in GMP – What Do You Need to Consider?
Learn the essential steps for supplier qualification, ensuring that suppliers meet GMP standards, mitigates risks, and maintains quality in the pharmaceutical industry.
Worst Case Selection in Cleaning Validation
Optimize cleaning validation in pharmaceutical manufacturing with key strategies for selecting worst-case scenarios, ensuring product safety and efficacy.
Process Validation Lifecycle: Risk-Based Approach
Discover the essentials of Process Validation Lifecycle with a risk-based approach. Learn how to ensure product integrity from development to commercialization, meeting critical specifications.
Process Validation in GMP
Discover the essentials of Process Validation in GMP, ensuring pharmaceutical quality through scientific and regulatory practices.
Out of Specification Results: Dealing with OOS Investigations in Pharma
Learn about all the phases of addressing Out of Specification (OOS) results in the pharmaceutical industry
Cleaning Validation In the Pharmaceutical Industry
Explore the essentials of cleaning validation in the pharmaceutical industry, including all necessary steps, challenges, and regulatory standards.
Quality Assurance vs. Quality Control in GMP: Key differences
Explore the critical differences between Quality Assurance and Quality Control in GMP and learn more about their role within the pharmaceutical industry.
User Requirement Specification: How to Create URS for Successful Equipment Procurement
Explore the essentials of User Requirement Specification (URS) for successful project execution. Learn to craft effective URS documents.
SwissMedicines Inspectorate: Interpretation of GMP Annex 1 [2022]
Swissmedicines Inspectorate interprets the 2022 GMP Annex 1 guidelines, offering crucial insights into pharmaceutical manufacturing quality. Stay informed with GMP Insiders.