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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....
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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...
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Data Integrity and Data Governance in GMP

Data Integrity and Data Governance in GMP

Ensuring data integrity and governance in GMP: a comprehensive guide to accurate, consistent, and reliable data management practices for pharmaceutical...
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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...
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Computer System Validation - CSV

Computer System Validation (CSV) In GMP

Computer system validation- CSV and its importance in data integrity for regulatory compliance and reliability in GMP regulated industries....
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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...
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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...
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User Requirement Specification for Purchase of Manufacturing Equipment

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....
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Good Documentation Practice - FI

Good Documentation Practice: Ensuring Data Integrity and Compliance in the Pharmaceutical Industry

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

GMP Cleanroom Classifications: Understand Class A, B, C and D

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