Category: Maintenance

The Maintenance category focuses on the systems and practices that keep pharmaceutical equipment, facilities, and utilities compliant, reliable, and fit for use.

Key topics include qualification activities, preventive and corrective maintenance, calibration, controlled environment upkeep, and periodic requalification. Attention is also given to how documentation, risk assessment, and regulatory requirements shape maintenance programs.

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types of hepa filters used in the pharmaceutical industry - featured image

Types of HEPA Filters Used in the Pharmaceutical Industry

Explore HEPA filter types used in pharmaceutical cleanrooms. Understand H13 vs H14, ULPA, gel-sealed filters, and Annex 1 testing requirements....
How to write a gmp compliant user requirement specification in pharma - featured image

How to Write a GMP-Compliant User Requirement Specification (URS)

Learn how to write a GMP-compliant User Requirement Specification (URS) with regulatory guidance, risk-based principles, and its role in the...
Types of Airlocks Used in the Pharmaceutical Industry

Types of Airlocks Used in the Pharmaceutical Industry

Explore types of airlocks in pharma: Cascade, Bubble, Sink. Learn how they ensure contamination control, cleanroom integrity, and GMP compliance....
IQ, OQ and PQ: Importance in GMP

IQ, OQ and PQ: Importance in GMP

Discover the importance of IQ, OQ, and PQ in GMP, ensuring equipment and systems are installed and function correctly to...
Challenge Tests for Blister Machines

Challenge Tests for Blister Machines

Explore the significance of challenge tests for blister machines in the pharmaceutical industry, ensuring the detection and rejection of defective...
FAT and SAT in GMP Importance in Equipment Validation

FAT and SAT in GMP: Importance in Equipment Validation

Exploring Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) - essential steps in ensuring equipment quality and compliance in...
Design Review and Design Qualification in the Pharmaceutical Industry

Design Review and Design Qualification in the Pharmaceutical Industry

Explore the crucial roles of Design Review and Design Qualification in the pharmaceutical industry, ensuring equipment meets user needs and...
People working in GMP industry

Qualification vs Validation: Key Differences and Importance in the Pharmaceutical Industry

Understand the difference: Qualification vs Validation. Navigate compliance in GMP facilities for optimal quality and safety standards....

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