Tag: european annex 11

Incorporating KPIs in Quality Management Review Meetings

Incorporating KPIs in Quality Management Review Meetings Incorporating KPIs in Quality Management Review Meetings Quality Management Review (QMR) meetings are crucial for ensuring that an organization’s quality management system is effective and meets regulatory requirements. With increasing scrutiny from regulatory…

Validating CPV Software Tools: 21 CFR Part 11 Compliance

Validating CPV Software Tools: 21 CFR Part 11 Compliance Validating CPV Software Tools: 21 CFR Part 11 Compliance Continued Process Verification (CPV) is an essential component of modern pharmaceutical manufacturing, ensuring consistent product quality and regulatory compliance. This article serves…

Washer Disinfector Qualification: IQ/OQ/PQ Requirements

Washer Disinfector Qualification: IQ/OQ/PQ Requirements Washer Disinfector Qualification: IQ/OQ/PQ Requirements 1. Introduction to Washer Disinfector Qualification The qualification of washer disinfectors is a critical component in ensuring that all equipment in aseptic processes adheres to the strict standards established by…

Examples of Revalidation-Related Observations from FDA 483s

Examples of Revalidation-Related Observations from FDA 483s Examples of Revalidation-Related Observations from FDA 483s In the pharmaceutical and biotechnology sectors, maintaining compliance with regulatory expectations is vital for ensuring product quality and safety. Revalidation and change control processes are central…

Decision Trees Based on ICH Q9 Guidelines

Decision Trees Based on ICH Q9 Guidelines Decision Trees Based on ICH Q9 Guidelines This article serves as a comprehensive guide for pharmaceutical professionals, focusing on the implementation of european annex 11 in the context of risk management. With an…

Writing a Protocol for Analytical Method Transfer

Writing a Protocol for Analytical Method Transfer Writing a Protocol for Analytical Method Transfer Transferring analytical methods from one laboratory to another or from development to routine use is a critical step in ensuring that quality control and quality assurance…

Steam Trap Qualification and Preventive Maintenance

Steam Trap Qualification and Preventive Maintenance Steam Trap Qualification and Preventive Maintenance In the pharmaceutical and biotech industries, ensuring the integrity of steam systems is critical for compliance with Good Manufacturing Practices (GMP) as outlined by regulatory agencies like the…

Acceptance Criteria for Blend Uniformity Testing

Acceptance Criteria for Blend Uniformity Testing Acceptance Criteria for Blend Uniformity Testing Blend uniformity testing is a pivotal aspect of the pharmaceutical manufacturing process, particularly within the context of regulatory compliance and quality assurance. Effective validation of blend uniformity assures…