Menu
Home
Forums
New posts
Search forums
What's new
New posts
All posts
New media
New media comments
Latest activity
Media
New media
New comments
Search media
Resources
Latest reviews
New resources
Search resources
Attachment List
Log in
Register
What's new
Search
Search
Everywhere
Threads
This forum
Search titles only
By:
New posts
Search forums
Menu
Log in
Register
Home
Forums
Medical Devices, Medical Information Technology, Medical Software and Health Informatics
Medical Device Related Regulations
JavaScript is disabled. For a better experience, please enable JavaScript in your browser before proceeding.
You are using an out of date browser. It may not display this or other websites correctly.
You should upgrade or use an
alternative browser
.
EU Medical Device Regulations
The 3 Medical Device Directives and other applicable regulations related to Medical Devices in the EU (European Union).
Prev
1
2
3
4
5
…
Go to page
Go
177
Next
First
Prev
3 of 177
Go to page
Go
Next
Last
Filters
Show only:
Loading…
B
Notified Body changed the submission deadlines for NC, CAPA Plans
bimeri
Mar 21, 2024
Replies
7
Views
278
Mar 24, 2024
Philip B
P
M
Does my "new" assay require a clinical study? or will a reference interval study suffice? in Japan Medical Device Regulations.
Mike W
Mar 21, 2024
Replies
0
Views
99
Mar 21, 2024
Mike W
M
AFAP principe in Supplier pFMEA
KiraKiwaKilowatt
Mar 20, 2024
Replies
4
Views
205
Mar 20, 2024
yodon
Y
P
All Post-marketing studies = PMCF?
partyhats
Jun 22, 2023
Replies
1
Views
385
Mar 20, 2024
VI Me
V
I
2017/745 (MDR) - Instruction for use (IFU) - manufacturer's website
Ioko
May 27, 2019
2
3
4
Replies
39
Views
18K
Mar 19, 2024
Cloud808
C
C
Service Number - Labelling
CraigRegulatory
Mar 12, 2024
Replies
3
Views
231
Mar 18, 2024
CraigRegulatory
C
P
Question on Borderline
Philip B
Mar 4, 2024
Replies
1
Views
207
Mar 17, 2024
Vetty007
V
G
Be prepared for Stage 2 MDR onsite audit
Galac
Jan 30, 2024
Replies
4
Views
378
Mar 15, 2024
EmiliaBedelia
E
R
EUDAMED function
ruthwu
Mar 13, 2024
Replies
1
Views
208
Mar 14, 2024
emili
E
B
2021/2226 on Electronic Instructions for Use (IFU) for medical devices
bimeri
Mar 5, 2024
Replies
6
Views
352
Mar 8, 2024
EmiliaBedelia
E
I
MDD Certificate Extension with respect to 2023/607
imcooleh
Jan 16, 2024
Replies
9
Views
495
Mar 7, 2024
imcooleh
I
M
Manufacturer contact data on label?
MarRz
Feb 29, 2024
Replies
0
Views
262
Feb 29, 2024
MarRz
M
K
Special conditions for Class III custom made implantable in contact with the CNS
kreid
Feb 29, 2024
Replies
2
Views
154
Feb 29, 2024
kreid
K
S
POST-MARKET PERFORMANCE FOLLOW-UP
Sieun Baek
Feb 28, 2024
Replies
0
Views
202
Feb 28, 2024
Sieun Baek
S
Documented procedure - Eudamed Device Registration
JoCam
Feb 27, 2024
Replies
4
Views
214
Feb 27, 2024
JoCam
Prev
1
2
3
4
5
…
Go to page
Go
177
Next
First
Prev
3 of 177
Go to page
Go
Next
Last
You must log in or register to post here.
Home
Forums
Medical Devices, Medical Information Technology, Medical Software and Health Informatics
Medical Device Related Regulations
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to the use of cookies.
Accept
Learn more…
Top
Bottom