Pharma Best Practices Webinars
Knowledge is much more powerful when it’s shared.We encourage knowledge sharing and we are providing a platform to share knowledge and complimentary access to this knowledge to all. One of the best things about knowledge sharing is that we can learn from mistakes of others and make sure we don’t repeat them. When experts share what hasn’t worked, we can gain insights into an issue and it prevents others from making the same errors. More importantly we can tap into best experiences and make sure we do repeat what has worked and not repeat what has not worked.
But when one finds something that works and has worked better than anything else before, one needs to share that knowledge with rest of the community. When people are learning from each other and have a platform to share their knowledge, that builds a sense of community. Join PHARMA BEST PRACTICES COMMUNITY.
- 1:08:00
- 6 ай бұрын
Master Revised Schedule M - New Critical Requirements for Manufacture of Oral Solid Dosage Forms
- 1:21:43
- 6 ай бұрын
Understanding Revised Schedule M Part II Ensuring Compliance in Sterile Product Manufacturing
- 1:28:21
- 2 жыл бұрын
' GMP's for Modern Pharmaceutical Water
- 1:28:55
- 2 жыл бұрын
Rouging in Pharmaceutical Water System
- 1:16:52
- 2 жыл бұрын
OECD GLPs for in vitro studies
- 1:20:57
- 2 жыл бұрын
FDA’s Quality Management Maturity and Quality Ratings Program
- 1:03:31
- 2 жыл бұрын
Application of Artificial Intelligence AI & Machine Learning ML in pharmaceutical Industry
- 1:21:24
- 2 жыл бұрын
Predictive Maintenance in Pharma Manufacturing
- 1:40:59
- 2 жыл бұрын
Revised Annex 1 GMP for sterile products
- 1:29:26
- 2 жыл бұрын
GMP Requirements for Pharmaceutical Gases and Clean Compressed Air
- 1:01:10
- 2 жыл бұрын
Determination of Metal Impurities in Pharmaceutical Products
- 1:36:57
- 2 жыл бұрын
Risk Based approach in CSV
- 1:39:35
- 2 жыл бұрын
Inspection of Injectable Products for Visible Particulates FDA Guidance
- 1:46:45
- 2 жыл бұрын
Good Practices for computerised systems in regulated ‘GxP’ environments
- 1:27:28
- 2 жыл бұрын
Microbiological Quality Considerations in Non sterile Drug Manufacturing per FDA’s Guidance
- 2:18:53
- 2 жыл бұрын
Maintaining Compliant Critical Utilities
- 1:34:35
- 2 жыл бұрын
Design , Qualification and Operation of Ambient WFI Systems with a focus on Asian regions
- 59:15
- 2 жыл бұрын
Efficient Use of 505 b2 Pathway to Enter US Market
- 1:13:16
- 2 жыл бұрын
Overcoming Common Cleaning Challenges
- 1:35:15
- 2 жыл бұрын
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