Medical Device made Easy Podcast
Total duration:
23 h 59 min
When is Regulatory Affairs needed during Design?
Medical Device made Easy Podcast
36:51
What is the new UK Post-Market Surveillance Requirements?
Medical Device made Easy Podcast
42:59
How to register your Medical Device in Malaysia?
Medical Device made Easy Podcast
36:02
Should you quit your job to become a consultant?
Medical Device made Easy Podcast
39:33
How to satisfy Cybersecurity for FDA and EU?
Medical Device made Easy Podcast
54:42
Medical Device News April 2025 Regulatory Update
Medical Device made Easy Podcast
25:18
What if the Notified Body asks you: Is your Software Validated?
Medical Device made Easy Podcast
45:36
What are the TOP 3 FDA inspection issues?
Medical Device made Easy Podcast
37:35
Medical Device News March 2025 Regulatory Update
Medical Device made Easy Podcast
36:21
How to avoid Clinical Investigation for your Device?
Medical Device made Easy Podcast
48:33
How and Who to build your Risk Management File?
Medical Device made Easy Podcast
27:12
The good, the bad and the ugly of certification bodies
Medical Device made Easy Podcast
36:35
Medical Device News January 2025 Regulatory Update
Medical Device made Easy Podcast
27:43
6 Tips to Grow as a QA RA Manager
Medical Device made Easy Podcast
30:00
TOP 5 common NCs on an ISO 13485 audit
Medical Device made Easy Podcast
50:47
How to perform your PMS for a Drug-Device Combination?
Medical Device made Easy Podcast
19:49
How to register a Medical Device in South Africa?
Medical Device made Easy Podcast
35:11
Medica: AI & MDR FLIP THE COIN
Medical Device made Easy Podcast
31:46
Easy Medical Device Great Summary 2024
Medical Device made Easy Podcast
31:19
What are the major pitfalls of Startups in Medical Devices?
Medical Device made Easy Podcast
44:19
Medical Device News december 2024 Regulatory Update
Medical Device made Easy Podcast
31:54
PCCP – The Magic tool for SaMD in the US?
Medical Device made Easy Podcast
33:55
IEC 60601-1-8 How to test your Medical Device alarms?
Medical Device made Easy Podcast
32:04
Is FMEA bad for your Risk Management?
Medical Device made Easy Podcast
30:36
How MDR and IVDR code can save you money?
Medical Device made Easy Podcast
35:37
Medical Device News November 2024 Regulatory Update
Medical Device made Easy Podcast
23:33
What does a strategy for regulatory compliance looks like?
Medical Device made Easy Podcast
31:50
What are the TOP 3 issues on CAPAs?
Medical Device made Easy Podcast
47:33
Medical Device News, october 2024 Regulatory Update
Medical Device made Easy Podcast
22:08
How to select the best plastic for your Medical Device?
Medical Device made Easy Podcast
35:07
UK vs EU vs US – How to switch to another region easily?
Medical Device made Easy Podcast
50:21
How to do a PMCF Literature Search for Medical Devices?
Medical Device made Easy Podcast
34:43
Medical Device News, Septembre 2024 Regulatory Update
Medical Device made Easy Podcast
33:29
How to use AI GPT for your Quality and Regulatory work?
Medical Device made Easy Podcast
51:44
How to go from Zero to Hero in Medical Devices?
Medical Device made Easy Podcast
28:55
Manage the Transfer/Renewal/Surveillance/Change of your CE certificate
Medical Device made Easy Podcast
43:14
How to use Harmonized Standards for Medical Devices?
Medical Device made Easy Podcast
31:01
IVDR Class D – Lesson learned from Notified Bodies
Medical Device made Easy Podcast
28:58
EU MDR Major update: Interruption or Discontinuation of supply!
Medical Device made Easy Podcast
49:01
How to register your Medical Device in the UAE?
Medical Device made Easy Podcast
25:17
