Equipment validation – a critical step in GMP pharma manufacturing
In the pharmaceutical industry, equipment must not only be modern — it must be validated to ensure safety, consistency, and GMP compliance.
So, what does GMP equipment validation involve? 👇
1️⃣ Design Qualification (DQ)
Ensure the equipment design meets pharmaceutical production requirements.
2️⃣ Installation Qualification (IQ)
Verify the equipment is installed correctly, with complete documentation and utility connections.
3️⃣ Operational Qualification (OQ)
Test system functions, control panels, alarms, and performance across intended operating ranges.
4️⃣ Performance Qualification (PQ)
Prove the equipment consistently produces acceptable products under real production conditions.
✅ Each stage is fully documented, measured, and approved by the QA/GMP team.
💡 Because quality products start with qualified equipment.
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The wall from ceiling down to the floor level, making the line fully visible from the operator side with no air ducts on the front side.
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Checking the punches and dies and the components of the tablet press for wear or damage is one of the very important steps to improve the quality of the tablets. There are some points to check that we easily overlook but can cause significant quality problems for the tablets and reduce the life of the punches and dies. So take some time to check the following points to determine their wear or defects and quickly improve the quality of the tablets and reduce the cost of punches and dies
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