Show cover of Medical Device made Easy Podcast

Medical Device made Easy Podcast

My name is Monir El Azzouzi and I am a Medical Device Expert specialized in Quality and Regulatory affairs. And on this podcast I will help you place compliant medical devices on the market. For that I will share with you my knowledge or the one of others through discussion or interviews. I will invite experts in the area to tell you what you can do or the challenges you may encounter.

Tracks

Attention! 1 year before UKCA is the law for Medical Devices in the UK 35:11 06/28/2022
Why is it great for Importers to be ISO 13485 certified? [Cristina Miroescu] 32:42 06/21/2022
How to avoid these common mistakes on your Quality System? [Karandeep Badwal] 28:39 06/14/2022
Medical Device News - June 2022 Regulatory Update 24:07 06/07/2022
Let's introduce our eQMS Smarteye with Anindya Mookerjea 32:04 05/31/2022
What is the EU Medical Device Situation? with Erik Vollebregt 26:53 05/24/2022
What happens after the IVDR Date of Application with Colm O’Rourke 32:58 05/17/2022
Certify your Software as a Medical Device with Vivek Thakkar 33:40 05/10/2022
Medical Device News - May 2022 Regulatory Update 25:55 05/03/2022
Training Procedure "How to avoid mistakes" with Rod Beuzeval and Katie Cooney 46:00 04/26/2022
How your PMCF is evaluated by your Notified Body? [Matthias Fink] 41:40 04/19/2022
Prepare your audit with a Front Room Back Room 29:28 04/12/2022
Medical Device News: April 2022 Regulatory Update 25:26 04/05/2022
What are some of the surprises during MDR and IVDR transition? [Erik Vollebregt] 44:18 03/29/2022
How to sell Medical Devices on an Online Platform? [Michael Wetherington] 29:39 03/22/2022
Which lessons did we learn doing Clinical Evaluations? [Cesare Magri] 40:15 03/15/2022
IVDR Class D Common Specification with Andreas Stange [TÜV SÜD] 27:44 03/08/2022
Medical Device News - March 2022 Regulatory Update 23:42 03/01/2022
Why do you need a Swiss Authorised Representative and Importer? 25:50 02/22/2022
How to have a great Management Review? 27:54 02/15/2022
Why Design History File (DHF) is so important? [Alexandros Savvidis] 36:51 02/08/2022
Medical Device News - February 2022 Regulatory Update 30:15 02/01/2022
MDCG 2021-27 Placing on the market and Importer Re-labelling with Erik Vollebregt 43:59 01/25/2022
How to interview QA RA candidates with Mitch Robbins 46:32 01/18/2022
How to accelerate your Laboratory Test Results? [Christoph Lindner] 42:50 01/11/2022
Medical Device News – January 2022 [Happy New Year] 30:22 01/04/2022
What happened in 2021? Summary for the Medical Device Industry 18:54 12/28/2021
The Step-by-Step recipe to get MDR & IVDR Certified 29:52 12/21/2021
Which devices cannot be Custom-made? [Erik Vollebregt] 44:01 12/14/2021
Medical Device News: December 2021 Regulatory Update 30:32 12/07/2021