Workshop: Vendor Validation/Audit (Revised Schedule M) -CDSCO-FDCA Guj & IDMA-GSB : 30-11-24 - 10 am

We are pleased to invite you to this interesting Workshop on Vendor Validation/ Audit (As per the Revised Schedule M) organized by the Central Drugs Standard Control Organization (CDSCO) and FDCA, Gujarat, in association with the Indian Drug Manufacturers Association (IDMA) - Gujarat State Board from 10 am to 5.30 pm Dr. S. Eswara Reddy, Joint Drug Controller of India, Dr. Naresh Sharma, Deputy Drugs Controller (India) at CDSCO, New Delhi, Dr. H. G Koshia, Commissioner, Food & Drugs Control Administration and Dr. Ravi Kant Sharma DDC (I), CDSCO, Ahmedabad Zone, have consented to attend this event, along with other officials from CDSCO and the FDCA. This workshop will focus on vendor validation and audits in line with the revised schedule M, with a particular emphasis on knowledge sharing and best practices. Vendor validation and audit are critical components in ensuring the quality, compliance, and reliability of external suppliers. Key Highlights: Best Practices In Vendor Qualifications For Ensuring Compliance In The Pharma Industry Best Practices In Vendor Qualifications Of Packaging Material For Ensuring Compliance In The Pharma Industry Criteria For Reduced Testing Desktop Audit Of Suppliers Of Starting / Packing Material Qualification Of Auditors