🎯 Key Takeaways for quick navigation: 00:00 📜 *Introduction to GMP in Pharmaceuticals* - Introduction to GMP by WHO in 1975, - Importance of GMP as a quality seal for pharmaceutical products, - Adoption of GMP regulations by countries worldwide. 00:56 🏭 *Basic GMP Facility Requirements* - Proper definition and control of manufacturing processes, - Validation of all critical processes for consistent results, - Clear documentation, evaluation of process changes, and personnel training. 01:51 📚 *Documentation and Record-keeping in GMP* - Manual or instrument-based records as evidence of proper procedures, - Retention of batch records until expiry, - Procedures for batch recall, examination of market complaints, and defect prevention. Made with HARPA AI
@MindMingleMania245 ай бұрын
perfect 👍
@titonsaha7994 жыл бұрын
Wow, good explanation within a very short time 😍
@thomasandrew64323 жыл бұрын
Short and precise
@seetapathiallam48924 жыл бұрын
Nice presentation.
@Pharmainform2 жыл бұрын
good
@ganeshshewale80005 жыл бұрын
Nice explanation on GMP next cessions do on swab system in pharmaceutical production pl
@swapnilmehta70822 жыл бұрын
Nice explanation. Thank you
@pharmaguideline2 жыл бұрын
You are welcome
@deepakulai37295 жыл бұрын
Can you please do presentation on different columns and integration part