Schedule M Webinars

Revised Schedule M  Critical Requirements for Manufacture of Biological Products

Understanding Computer System Validation requirements as per 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

 New Critical Requirements for Manufacture of Oral Solid Dosage Forms

Ensuring Compliance in Sterile Product Manufacturing

Qualification and Validation principles to meet revised schedule M requirementsere.

GMP's for  Modern Pharmaceutical Water

Rouging in Pharmaceutical Water System