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.
Абсолютная тренировка по безопасности в фармацевтике
Revised Schedule M Critical Requirements for Manufacture of Biological Products
Understanding Computer System Validation requirements as per revised Schedule M
Revised Schedule M Practical approach to implement Quality Risk Management
Qualification of Analytical Instruments Schedule M, WHO,USP and EU Requirements
P W Systems compliance to India , US , EU Pharmacopeia using QRM & PAT
Master Revised Schedule M – New Critical Requirements for Manufacture of Oral Solid Dosage Forms
Qualification and Validation principles to meet revised schedule M requirements
Understanding Revised Schedule M Part II Ensuring Compliance in Sterile Product Manufacturing
' GMP's for Modern Pharmaceutical Water
Rouging in Pharmaceutical Water System
OECD GLPs for in vitro studies
Lesson learnt on FDA citations on cleaning, disinfection and sterilization’
FDA’s Quality Management Maturity and Quality Ratings Program
Application of Artificial Intelligence AI & Machine Learning ML in pharmaceutical Industry
Predictive Maintenance in Pharma Manufacturing
Revised Annex 1 GMP for sterile products
GMP Requirements for Pharmaceutical Gases and Clean Compressed Air
Determination of Metal Impurities in Pharmaceutical Products
Risk Based approach in CSV
Inspection of Injectable Products for Visible Particulates FDA Guidance
Good Practices for computerised systems in regulated ‘GxP’ environments
Smart Robotic Solutions for Pharma Applications – Opportunities and Challenges
Microbiological Quality Considerations in Non sterile Drug Manufacturing per FDA’s Guidance
Maintaining Compliant Critical Utilities
Design , Qualification and Operation of Ambient WFI Systems with a focus on Asian regions
Efficient Use of 505 b2 Pathway to Enter US Market
Overcoming Common Cleaning Challenges
Digitalization for Data Integrity & Regulatory Compliance
ICH Q5A updates and its Impact on BioProcessing