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
Overcoming Common Cleaning Challenges
Design , Qualification and Operation of Ambient WFI Systems with a focus on Asian regions
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