Dr. Nand Kishore Khandelwal, Ph.D, is a pharmaceutical professional with over 32 years of leadership experience in Quality Assurance, Quality Control, Microbiology, Compliance, and Validations. He has worked across sterile and non-sterile dosage forms including parenterals (cytotoxic), oral solids, APIs, and finished formulations in reputed companies like Lupin, Wockhardt, Emcure, and Orchid.

Since 2016, he has been providing technical consultancy services to pharmaceutical and medical device companies in India and abroad. His areas of focus include GMP compliance, regulatory audits, aseptic processing, FDA remediation, facility design, and regulatory documentation review. He has also trained over 2,000 professionals in quality systems, sterility assurance, and microbiology.

Dr. Khandelwal has successfully supported inspections by global regulatory bodies such as US FDA, WHO, MHRA, EU, and TGA, and is recognized as a subject matter expert in aseptic processing and quality systems. He holds a Ph.D. in Microbiology, is affiliated with the Parenteral Drug Association (USA), and has worked across USA, Europe, Asia, and the Middle East on various international assignments.