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Medical Devices Rules 2017 — Rapid Revision Series | Lecture 1 Welcome to Friends and Pharma — Lecture 1 of the Complete Medical Devices Rules 2017: Rapid Revision Series designed specifically for UPSC Drugs Inspector (Medical Devices) aspirants and pharmacy students preparing for competitive exams. In this concise, exam-oriented lecture you will learn: 0. Series overview — what this rapid revision series will cover. 1. Scope & definitions under MDR 2017 — what is a medical device, active device, IVD, notified devices. 2. Risk-based classification (Class A, B, C, D) — quick rules, examples, and exam mnemonics. 3. Registration vs. licensing — who needs registration, who needs import/manufacturing license. 4. Key regulatory bodies & portals (CDSCO, SUGAM/NSWS) — where to file applications. 5. High-yield points for UPSC — frequently asked topics, past-year trends and must-remember dates / rule numbers. 6. Quick revision mnemonics & one-page checklist to memorise before exams. ⏱️ Run time: Short & focused — perfect for last-minute revision and quick concept recall. 🔗 Resources & Notes: Join our Telegram for downloadable one-pagers, past-year PYQs, and the full lecture notes. 👉 https://t.me/friendsandpharma 🔔 Subscribe to Friends and Pharma for the full Rapid Revision playlist 👍 Like, share and comment your doubts — I’ll cover the highest-voted questions in Lecture 2. #druginspector #upscdruginspectorcrashcourse #cdsco #MedicalDevicesRules2017 #UPSCDrugsInspector #MedicalDevices #FriendsAndPharma #MDR2017 #friendsnpharma #pharmacycareer #centralgovtjobs #medicaldevices #druginspectorexam