SCHEDULE M – GMP – PART 1
GOOD MANUFACTURING PRACTICES – SCHEDULE M
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Out of Specification (OOS)
Out of specification pharmaceutical | Out of specification Guidelines | Out of specification – OOS Investigation | Out of specification reasons |
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Microbiological Control Tests
Microbiology testing in pharmaceutical industry
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Daily Maintenance and Common problems in HPLC
HPLC Problems and Solutions | HPLC Troubleshooting Guide | Common error occurs during HPLC Analysis |
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INFRARED ABSORPTION SPECTROSCOPY
Infrared Absorption Spectroscopy Principle | What is infrared absorption spectroscopy? | IR Spectroscopy – Principle and Applications |
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Tap Density Tester SOP
SOP for the operation and calibration of Tap Density Tester.
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Quality Control – Principle, General information
Quality Control in Medicinal products | Quality Control Principle | Quality Control General information | Good Quality Control Laboratory Practice |
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HPLC Basics- Principle and Scope
HPLC – Principle | Scope | Diagram | Separation Mechanism | Separation Modes | Detectors for HPLC |
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Aseptic Processing – Sterile Pharmaceutical
Aseptic Processing in Pharmaceuticals.
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Good Laboratory Practice – GLP
What is Good Laboratory Practice | Why Good Laboratory Practice | The purpose of GLP |
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