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In this video, we cover Medical Devices Rules, 2017 – Chapter 10, 11, and 12 in a simple, detailed, and exam-oriented manner for the UPSC Drug Inspector (Medical Devices) 2025 exam. You’ll learn: 🔹 Chapter 10 – Registration of Testing Laboratories (Rules 81–86) • Role of Central Licensing Authority (CLA) • Forms MD-39 & MD-40 explained • NABL Accreditation & Inspection Process • Validity, Retention, and Suspension of Registration 🔹 Chapter 11 – Sale and Recall of Medical Devices (Rules 87–89) • Integration with Drugs & Cosmetics Rules, 1945 • Supply to Hospitals (Rule 88) • Device Recall Procedure & Responsibilities (Rule 89) 🔹 Chapter 12 – Miscellaneous Provisions (Rules 90–97) • Exemptions (Eighth Schedule) • Export Procedures & Free Sale Certificate • Debarment, Digital Payments, Overriding Powers, and Savings Clause 🎯 Perfect for: UPSC Drug Inspector (Medical Devices) 2025 | CDSCO & State Drug Inspector Exams | Pharmacist & Regulatory Affairs Aspirants 💡 Why Watch This Video? ✅ Based on official Medical Devices Rules, 2017 ✅ Linked with PYQs & expected UPSC questions ✅ Explained in simple English + key MCQ focus ✅ Quick recall charts & revision notes included 📚 Timestamps 00:00 – Introduction 01:40 – Chapter 10 (Registration of Labs) 09:20 – Chapter 11 (Sale & Recall Rules) 15:50 – Chapter 12 (Miscellaneous Rules) 22:00 – PYQs + MCQs + Summary #UPSCDrugInspector #MedicalDevicesRules2017 #DrugInspectorExam #UPSCPharmacy #PharmaRegulations #MedicalDevices #CDSCO #Chapter10to12 #PharmacyExamPreparation #UPSC2025 #DrugInspectorMedicalDeviceExam #MedicalDeviceRegulation #PharmacistExam #UPSCDrugInspector2025 #shubhamsir #pharmacistshubham #