Quality - Pharma GxP

FDA's 21 CFR Part 11: The Definitive Guide – Detailed resource for understanding FDA regulations on electronic records and signatures

FDA’s 21 CFR Part 11: The Definitive Guide

August 26, 2024

Good Manufacturing Practices - ICH Q7 Highlights – Overview of essential GMP guidelines from ICH Q7

Good Manufacturing Practices – ICH Q7 Highlights

August 26, 2024

Cleaning Validation: The Definitive Guide – Essential resource for cleaning validation processes in pharmaceuticals

Cleaning Validation: The Definitive Guide

November 29, 2024

Quality by Design and 9 Such Tools – Overview of key tools for implementing Quality by Design principles

Quality by Design and 9 Such Tools

August 26, 2024

9 Important Differences Between Qualification and Validation – Essential distinctions in qualification and validation processes

Process Validation: The Essential Guide to Ensuring Product Quality and Compliance

August 26, 2024

Important Aspects of Good Documentation Practices (GDP) and 9 Principles of ALCOA+ – Key guidelines for maintaining high-quality documentation

Important Aspects of Good Documentation Practices (GDP) and 9 Principles of ALCOA+

August 26, 2024

Clean Room and Classification: Summary of 4 Different Standards – Overview of clean room standards and classifications

Clean Room and Classification: Summary of 4 Different Standards

August 26, 2024

9 Important Differences Between Qualification and Validation – Clear comparison of qualification and validation processes

9 Important Differences Between Qualification and Validation

August 26, 2024