Category: Maintenance

Discover the importance of IQ, OQ, and PQ in GMP, ensuring equipment and systems are installed and function correctly to maintain high-quality manufacturing standards.

Ensuring data integrity and governance in GMP: a comprehensive guide to accurate, consistent, and reliable data management practices for pharmaceutical professionals.

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.

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 GMP facilities.

Explore the crucial roles of Design Review and Design Qualification in the pharmaceutical industry, ensuring equipment meets user needs and complies with rigorous standards.

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

Explore effective strategies for maintaining clear and comprehensive records with our guide on good documentation practices, ensuring accuracy and reliability.

Learn GMP cleanroom classes A, B, C, D for contamination control in pharmaceuticals. Understand air cleanliness & particle counts for compliance.

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