What you should know about Vigilance Reporting for Medical Devices?

  Рет қаралды 1,693

Easy Medical Device

Easy Medical Device

Күн бұрын

Пікірлер: 5
@gulnihalsevim3908
@gulnihalsevim3908 22 күн бұрын
Amazing energy .
@EasyMedicalDevice
@EasyMedicalDevice 8 күн бұрын
High or Zen energy lol. I like discussing with Adam. Really a cool guy.
@mwmd164
@mwmd164 Жыл бұрын
Thank you for a great podcast! The document you shared is very helpful. However, the link to the spreadsheet that has a list of the reporting requirements for different countries, does not work. It takes me to an empty folder. It would be great if you could check this. Thank you so much!
@EasyMedicalDevice
@EasyMedicalDevice Жыл бұрын
check again the link if this is fixed. Adam informed me that he tried to update it.
@Vasoulitsa72
@Vasoulitsa72 Жыл бұрын
Thank you so much for looking into that! It woks perfect now😊
How to do Post Marketing Surveillence in the US? (vs Europe)
50:27
Easy Medical Device
Рет қаралды 1,5 М.
Medical Devices 101: An Entry Level Overview of the FDA
49:08
leanRAQA
Рет қаралды 2,8 М.
Когда отец одевает ребёнка @JaySharon
00:16
История одного вокалиста
Рет қаралды 16 МЛН
How to implement Vigilance Reporting within MDR and IVDR?
28:12
Easy Medical Device
Рет қаралды 2,5 М.
EU MDR Hot Takes: Evolution or Overreach?
57:45
leanRAQA
Рет қаралды 92
Medical Device Standards overview: ISO13485
1:07:55
SINE IIT Bombay
Рет қаралды 10 М.
Medical Device Complaint Handling: MDR, Reports of Removals and Corrections
1:00:35
EU Postmarket Surveillance Requirements for Medical Devices
1:25:47
Medical Device Academy
Рет қаралды 3 М.
Is My Product A Medical Device
24:00
U.S. Food and Drug Administration
Рет қаралды 18 М.
PMCF or Post-Marketing Clinical Follow-Up with Helene Quie (MDR 2017/745)
12:54
Design Controls - Requirements for Medical Device Developers
1:39:26
GlobalCompliance Panel
Рет қаралды 31 М.
FDA 101 for Medical Devices
57:47
Registrar Corp
Рет қаралды 36 М.