3:49
Are you MDSAP? - The Medical Device Single Audit Program for Medical Device Industry
Easy Medical Device
22:21
How to register a Medical Device in Pakistan?
18:43
GDPR & MDR for Medical Device Application with Jovan Stevovic
36:52
Why MEDICA COMPAMED 2019 was great for Networking with the Medical Device community?
46:48
How to collect Clinical Data for Medical Devices with David Rutledge (MDR 2017/745)
7:11
Medical Device School - How to audit your Suppliers?
21:52
How to register your Medical Device in Brazil? (ANVISA)
28:10
How to get your Digital Health Application reimbursed in Germany? (DIGA)
38:06
Best Practices to Test your Medical Devices
28:19
Trends of Virtual conferences in the Medical Device industry
19:05
Medical Device News - August 2020 review (without Clip)
43:39
How to get some help from Medical Device regulators?
29:31
How to register your device in the ASEAN Region ? [Michael Wetherington]
35:53
How to register Medical devices in Mexico? [Josué Garza]
31:15
Podcast - How to register a Medical Device in Israel? (Liat Nadel)
20:45
February 2021 Update - Remote audit by EU Commission and Co.
What is the best Quality & Regulatory Affairs Mindset? [Michelle Lott]
26:54
How to enter Medical Device World by building a Network? [Karandeep Badwal]
47:37
Medical Device Design Control: Waterfall or Agile? [Jon Speer Greenlight Guru]
24:28
Medical Device News - March 2021 Update [Monir El Azzouzi]
31:25
FDA: Is the Emergency Use Authorization worth it? (EUA)
35:18
Medical Device News - June Update 2021 [EU MDR date of Application]
32:53
How Intellectual Property is linked to the Medical Device Regulation ?
29:54
Medical Device News - December 2021 Regulatory Update
29:34
Medical Device News: February 2022 Regulatory Update
35:59
Why Design History File (DHF) is important? [Alexandros Savvidis]
24:44
Medical Device News- April 2022 Regulatory Update
28:35
How to prepare your Audit with a Front Room & Back Room? [Medical Devices]
25:13
Medical Device News: May 2022 Regulatory Update
26:05
What did we learn about the EU Medical Device Situation at Medtech Forum?
31:19
Why should you choose this eQMS with Anindya Mookerjea
34:26
Attention! 1 year before UKCA is the law for Medical Devices in the UK
26:41
Medical Device News: July 2022 Regulatory update
34:17
Medtech Forum Barcelona - 4 Interviews (MDR, EUDAMED, CER, MECOMED)
32:45
Do you need a Cleanroom for your Medical Devices? [Philippe Bourbon]
26:25
Why you absolutely need to have an Initial Importer for the US market?
41:54
Medical Device News - October 2022 Regulatory Update
28:28
How to get MDSAP Certified for your Medical Devices?
30:43
Medical Device News - November 2022 Regulatory update
19:54
Why Risk Management is critical to Medical Device Development?
32:31
Medical Device News - December 2022 update
28:36
Medical Device News - January 2023 Regulatory update
43:05
How to eavluate Risk-Benefit Ratio? [Naveen Agarwal] #medicaldevices
50:27
How to do Post Marketing Surveillence in the US? (vs Europe)
0:56
Postmarketing Surveillance Medical Devices US #medicaldevices #fda
24:52
Medical Device New - February 2023 Regulatory Update
36:27
MEDICAL DEVICE NEWS – SEPTEMBER 2023 Regulatory Update
