Operational Qualification: What Parameters to Verify

Operational Qualification: What Parameters to Verify Operational Qualification: What Parameters to Verify Step 1: Understanding the URS & Risk Assessment Operational Qualification (OQ) is an integral part of the validation lifecycle in the pharmaceutical industry, ensuring that equipment operates within…

Execution of OQ Protocols: Best Practices for Validation Teams

Execution of OQ Protocols: Best Practices for Validation Teams Execution of OQ Protocols: Best Practices for Validation Teams In the pharmaceutical industry, ensuring the utmost quality and compliance in manufacturing processes is an ongoing challenge. This article serves as a…

Installation Qualification (IQ) Checklist for GMP Equipment

Installation Qualification (IQ) Checklist for GMP Equipment Installation Qualification (IQ) Checklist for GMP Equipment In the pharmaceutical industry, ensuring that equipment is qualified to operate consistently and effectively is a critical aspect of compliance with Good Manufacturing Practices (GMP). The…

What Is Design Qualification (DQ) and Why It Matters

What Is Design Qualification (DQ) and Why It Matters What Is Design Qualification (DQ) and Why It Matters In the highly regulated pharmaceutical and biologics industries, achieving compliance with established regulations and guidelines is crucial for delivering safe and effective…

IQ vs OQ vs PQ: Understanding the Key Differences

IQ vs OQ vs PQ: Understanding the Key Differences IQ vs OQ vs PQ: Understanding the Key Differences In the pharmaceutical and biotechnology industries, equipment qualifications play a crucial role in compliance, ensuring that any equipment used in manufacturing processes…

How to Write DQ, IQ, OQ, PQ Protocols in Pharma

How to Write DQ, IQ, OQ, PQ Protocols in Pharma How to Write DQ, IQ, OQ, PQ Protocols in Pharma In the pharmaceutical industry, the validation of equipment and processes is critical for ensuring product quality and regulatory compliance. This…