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Neeraj Mehta is an experienced professional who has held various roles in quality assurance and regulatory affairs in the pharmaceutical industry. With a background in biochemistry and a Master of Business Administration degree, Neeraj has worked at companies such as Almac Diagnostics and BIOVECTRA, focusing on implementing design control activities, computerized system validation, and quality compliance. Neeraj has a strong track record of reviewing manufacturing batch records, conducting audits, and ensuring compliance with relevant regulations such as ISO13485, 21 CFR Part 11, and ICH Q7 GMP.