What is a Notified Body? Published 2022-09-11 Download video MP4 360p Download video MP4 720p Recommendations 05:06 CE Marking Responsibilities for Manufacturers 22:07 What is CE Marking? 1:01:14 How to classify a Medical Device? (EU MDR Case Studies) 44:07 Why Importers and Distributors need a Notified Body? [Article 16] 21:41 Post-market surveillance as a medical device requirement in the EU 07:58 How To Become a Notified Body Auditor? (Bassil Akra TÜV SÜD) 26:33 Medical Device Regulation 32:12 I help you select your Notified Body & understand the full process 1:03:18 Understanding Europe's Medical Device Regulation 13:18 Everything you need to know about the IVDR 14:55 Short course on the Medical Device Regulation (EU) 2017/745 09:35 What is Accreditation & What is Certification? 17:40 Medical Device Regulation codes 19:26 Short course on Clinical Investigation for Medical Devices and ISO 14155 11:28 EU Deforestation Regulation (EUDR): A Video Tutorial 43:21 Which strategy to adopt with your Notified Body? [Dr Royth von Hahn] 11:47 Conformity assessment procedures for medical device manufacturers 1:29:46 Combination Products: Seeking Notified Body Opinion According to Article 117 - Webinar 25:28 How to perform your Internal Audits correctly? (Medical Devices) 08:46 The 5 most important steps to CE certification - The EU medical device approval process Similar videos 03:05 The Role of Notified Bodies in Europe 37:40 What is the Notified Body Situation for CE marking? (Bassil Akra) 01:35 BSI Medical Devices | IVDR UK Notified Body Designation 10:53 Find EASILY your Notified Body for CE Certification 01:20 BSI Medical Devices | MDR Netherlands Notified Body Designation 07:15 Kiwa Notified Body Application and Review process - Alessia Frabetti 35:45 EU MDR & IVDR Notified Body Situation with Erik Vollebregt 28:11 Notified body perspective on CE-marked medical devices versus article 117 MDR combination products 00:55 Notified Bodies situation 11:21 Medical Device Regulation and Notified Bodies | Med-Tech World 01:51 BSI Medical Devices | A full scope Notified Body under the EU IVDR 00:58 Who are the new Notified Bodies? 00:58 When should manufacturers contact the notified body? 01:37 Notified Body More results