Dr. Khalid is the leading GMP expert at dicentra. He helps dicentra’s clients reach compliance with the FDA GMP Rule for Dietary Supplements (21 CFR 111), Pharmaceuticals & Cosmetics (21 CFR 210) and Electronic Records & Electronic Signatures (21 CFR 11). Dr. Khalid implements quality systems by performing gap analyses, implementing Standard Operating Procedures and training staff on all required matters. To date he has worked with small sized manufacturers, packagers, labellers and distributors to large multi-national companies with supply chains spanning continents.
Dr. Khalid has many years of experience in the pharmaceutical and dietary supplement industries, with extensive experience related to analytical method development, validation, Good Manufacturing Practices and Good Laboratory Practices. Dr. Khalid has also prepared and overseen implementation and compliance with company’s HACCP Plan.
Dr. Khalid has experience in Regulatory Affairs Consulting services in the areas of compliance, documentation, drug master files, audits, project management and validation. Other areas of experience include pharmaceutical and medical device compliance, active pharmaceutical ingredients, Chemistry Manufacturing and Controls (CMC) documentation.
Dr. Khalid’s educational credentials include a Doctor of Philosophy in Organic Chemistry and a Bachelor of Science in Chemistry.
dicentra provides sought-after regulatory and scientific guidance on product and marketing compliance, quality assurance, research and development, new ingredient assessments and overall regulatory strategies for health-related products sold in North American marketplaces.