Master 21 CFR 210/211 скачать в хорошем качестве

Master 21 CFR 210/211

Quick, clear breakdown of 21 CFR Part 210 & 211 — GMP basics every pharma trainee must know. This 2–3 minute video explains what 21 CFR is, how Part 210 sets GMP principles, and how Part 211 drives detailed requirements for personnel, facilities, equipment, production controls, lab testing, packaging, and documentation. Learn why most FDA 483 observations tie to Part 211 and how compliance protects product quality, patient safety, and data integrity. Perfect for new GMP trainees prepping for audits and inspections. Like and share if this helped you pass audits faster! #21CFR #GMP #FDA #Pharma #Compliance #QualityAssurance #Audits #DataIntegrity #GoodManufacturingPractices OUTLINE: 00:00:00 INTRO 00:00:13 1️⃣ What is 21 CFR? (0:15–0:30) 00:00:23 For drug manufacturing, Part 210 and Part 211 are the core GMP regulations. 00:00:28 2️⃣ 21 CFR Part 210 – GMP Overview (0:30–0:55) 00:00:49 3️⃣ 21 CFR Part 211 – Detailed GMP Requirements (0:55–1:55) 00:01:27 4️⃣ Why 210 & 211 Are So Important (1:55–2:25) 00:01:43 5️⃣ Key Takeaway (2:25–2:45) 00:01:57 OUTRO (2:45–3:00)