GMP Insiders - Your trusted source for GMP compliance!

Category: Maintenance

If you don’t find what you are looking for, try using a different term or contact us.

Learn how to write a GMP-compliant User Requirement Specification (URS) with regulatory guidance, risk-based principles, and its role in the...
Explore types of airlocks in pharma: Cascade, Bubble, Sink. Learn how they ensure contamination control, cleanroom integrity, and GMP compliance....
Discover the importance of IQ, OQ, and PQ in GMP, ensuring equipment and systems are installed and function correctly to...
Explore the significance of challenge tests for blister machines in the pharmaceutical industry, ensuring the detection and rejection of defective...
Computer system validation- CSV and its importance in data integrity for regulatory compliance and reliability in GMP regulated industries....
Exploring Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) - essential steps in ensuring equipment quality and compliance in...
Explore the crucial roles of Design Review and Design Qualification in the pharmaceutical industry, ensuring equipment meets user needs and...
Explore effective strategies for maintaining clear and comprehensive records with our guide on good documentation practices, ensuring accuracy and reliability....
Understand the difference: Qualification vs Validation. Navigate compliance in GMP facilities for optimal quality and safety standards....

BECOME A GMP INSIDER

Stay in touch and be the first to get the latest GMP News