Faculty: Saurabh Joshi | Code: FDB3510
Equipment qualification and process validation is a cumbersome activity if realistic but compliant approach is not applied. This session should help responsible personnel and teams to apply efforts in right direction to ensure regulator satisfaction at the same time help company operationalize full potential of both process and equipment/system.
Lack of adequate qualification or validation is a common FDA inspectional observation and FDA Warning Letter violation. Those involved in equipment qualification, manufacturing and process validation will benefit from a review of the relevant FDA rules, written and unwritten. Those involved in hosting FDA inspections will also benefit.
Areas Covered in the Session :
Who Should Attend:
Saurabh is an industry professional with >20 years of experience in working in the areas of Quality operation, Quality systems, Tech. transfer Quality, Compliance, Validation and Qualifications. He has worked with reputed companies like Cipla, Microlabs, Wockhardt India and EU, Torrent, Sun Pharma and Alembic. He has led regulatory inspections like USFDA, MHRA, WHO GMP (Geneva), HPRA etc and has executed robotics and automation projects for industry 4.0 transformation.
From shopfloor at site to leading corporate level function and consulting world’s oldest pharmaceutical company- Merck specialties Pvt. Ltd. (A Merck KGaA, Darmstadt Germany company), Saurabh has delivered value in his assignments.He’s currently working with ValGenesis as Director-Industry solution. In his role he’s responsible for expanding customer outreach and demonstrate platform capabilities with ValGenesis’s solutions to lifescience companies.