Medical Devices Rules 2017 – Chapter 10, 11, 12 🔥| UPSC Drug Inspector Medical Device Exam 2025
Автор: Pharmacist Shubham
Загружено: 2025-10-13
Просмотров: 4793
Описание:
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
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