Tag: Manufacturing

Explore the significance of challenge tests for blister machines in the pharmaceutical industry, ensuring the detection and rejection of defective packs to maintain product quality and safety.

Learn more about Batch Manufacturing Records (BMR), essential for consistent, safe pharmaceutical production and compliance with regulatory standards.

Optimize cleaning validation in pharmaceutical manufacturing with key strategies for selecting worst-case scenarios, ensuring product safety and efficacy.

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.

Discover the essentials of Process Validation in GMP, ensuring pharmaceutical quality through scientific and regulatory practices.

Explore the essentials of User Requirement Specification (URS) for successful project execution. Learn to craft effective URS documents.

Discover the difference between qualification and validation in regulated industries. Ensure compliance with GxP regulations for quality and safety.

Swissmedicines Inspectorate interprets the 2022 GMP Annex 1 guidelines, offering crucial insights into pharmaceutical manufacturing quality. Stay informed with GMP Insiders.

Explore the crucial role of pharmaceutical packaging in manufacturing processes. Ensure medication safety and integrity, following good manufacturing practices.