Скачать или смотреть GMP Equipment Design Qualification (DQ) | Your Ultimate Guide

🔍 GMP Equipment Design Qualification (DQ) – Pharma Validation Explained!

In this video, we take a deep dive into Design Qualification (DQ)-a critical step in the GMP equipment validation lifecycle. If you've already watched our video on Pharma Equipment URS, this is your next essential step toward mastering GMP compliance.

Learn: ✅ What is Design Qualification in pharma?
✅ How DQ fits into the validation V-Model
✅ Format and real-life examples of a DQ document
✅ Regulatory expectations from USFDA, WHO, MHRA, MOHAP
✅ Best practices and common pitfalls in equipment DQ

Whether you're a QA professional, validation engineer, or pharma student, this guide is your one-stop resource for understanding and implementing GMP Design Qualification effectively.

📌 Stay tuned for the next part in our Pharma Validation series: Installation Qualification (IQ)!

📞 Need help with your GMP Equipment URS, DQ, or complete validation strategy?
Connect @PharmaHealthInsights for end-to-end GMP consultancy services.

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