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Category: Maintenance
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Articles
,
Maintenance
January 28, 2025
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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Articles
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Maintenance
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Manufacturing
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QA
,
QC
July 16, 2024
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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Articles
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Maintenance
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Manufacturing
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QA
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QC
July 7, 2024
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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Articles
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Maintenance
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Manufacturing
May 23, 2024
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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Articles
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Maintenance
April 25, 2024
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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Articles
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Maintenance
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Manufacturing
February 19, 2024
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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Articles
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Maintenance
January 17, 2024
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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Articles
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Maintenance
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Manufacturing
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QA
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QC
December 20, 2023
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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Articles
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GDP
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Maintenance
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Manufacturing
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Microbiology
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QA
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QC
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Regulatory
December 14, 2023
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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Articles
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Maintenance
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Microbiology
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QA
December 8, 2023
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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