Faculty: Saurabh Joshi
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:
Speaker: SAURABH JOSHI
Saurabh Joshi is founder of StepUP Consultants, a pharmaceutical operations consulting company. He is renown for his contributions in executing robotics and automation projects for industry 4.0 transformation.
An industry professional with over 20 years hands on experience in Quality operations, Quality systems, Tech. transfer, Compliance, Validation and Qualifications; has successfully lead numerous regulatory inspections from USFDA, MHRA, WHO GMP (Geneva), HPRA for reputed organizations he has been a part of, such as, Cipla, Microlabs, Wockhardt, Sun Pharma to name a few. He has been an external Quality consultant with Merck specialties Pvt. Ltd. (A Merck KGaA, Darmstadt Germany company) guiding from shop floor at site to leading corporate level functions.
His consulting expertise includes, gap assessments and SOP preparation, regulatory inspections, QMS, technology transfer, Process Validation and equipment qualification, GMP, Data Integrity and Artificial Intelligence & Robotics.