Welcome to GMP 101, the essential audio guide for professionals in the pharmaceutical and biotech industries. Navigating regulations is complex. We break down the workflows that keep you inspection-ready. We cover: - Compliance: GMP, GDP & Inspection Readiness - Validation: CQV, CSV, Cleaning and Process Validation - Quality Systems: Risk Management, Audits, Vendor Qualification, Inspection Readiness Dr Saqib Choudhary’s brief profile: - +26 years of experience (18 yrs in the UK) - Successful hosting of over 48 inspections (US FDA, EMA, MHRA, HPRA, WHO, ANVISA, and more) - Over 500 audits
Dr Saqib Choudhary
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