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Medical Devices, Medical Information Technology, Medical Software and Health Informatics
Medical Device Related Regulations
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UK Medical Device Regulations
UK Medical Device Regulations, especially with respect to BREXIT issues.
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Retailer obligations as distributor
EricHeyworth
Aug 22, 2022
Replies
3
Views
423
Aug 23, 2022
Ronen E
J
Conformity assessment route options under the UK MDR 2002 (2002 SI No. 618), as amended
jansayshello
Aug 16, 2022
Replies
1
Views
793
Aug 16, 2022
Ronen E
Informational
Guidance on In-House manufacturing
dgrainger
Jul 29, 2022
Replies
0
Views
375
Jul 29, 2022
dgrainger
Informational
Consultation on the future regulation of medical devices in the United Kingdom
dgrainger
Sep 16, 2021
Replies
4
Views
790
Jun 26, 2022
dgrainger
Q
Class I Medical Device with measuring function (UK MDR 2002 / MDD)
QARA93
Jun 17, 2022
Replies
3
Views
611
Jun 17, 2022
EricHeyworth
H
Update to UK MDR 2002 No. 618
Hiro@162
May 30, 2022
Replies
2
Views
475
Jun 1, 2022
Hiro@162
H
Informational
Consolidated UK MDR 2002
dgrainger
May 17, 2022
Replies
0
Views
418
May 17, 2022
dgrainger
S
Need clarification on UKCA and "Approved Body"
Steve_in_MT
Apr 20, 2022
Replies
7
Views
893
Apr 26, 2022
Steve_in_MT
S
S
Changing UK Responsible Person
Scott
Apr 26, 2022
Replies
0
Views
345
Apr 26, 2022
Scott
S
G
UKCA and EU MDR marking
GiuliaGe
Apr 5, 2022
Replies
5
Views
1K
Apr 5, 2022
dgrainger
B
Document Retention period for MHRA submission
bill.Kal
Mar 7, 2022
Replies
0
Views
488
Mar 7, 2022
bill.Kal
B
E
Import requirements in UK?
EmiliaP
Feb 23, 2022
Replies
1
Views
469
Feb 25, 2022
dgrainger
Acquisitions - Legacy Devices
JoCam
Feb 17, 2022
Replies
0
Views
363
Feb 17, 2022
JoCam
J
Quick question on responsible person's experience requirements
Jonathanlai928
Jan 27, 2022
Replies
3
Views
641
Feb 9, 2022
dgrainger
Group - legal manufacturers
JoCam
Jan 12, 2022
Replies
0
Views
333
Jan 12, 2022
JoCam
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Medical Devices, Medical Information Technology, Medical Software and Health Informatics
Medical Device Related Regulations
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