RegDesk
TRY US FOR FREE
  • Company
  • Solution
    • Application Builder
    • Regulatory Intelligence
    • RegDesk Tracking
    • RegDesk Regulatory Consulting
  • Beyond RIMS
  • Blog
  • Resources
    • Device Regulation Library
    • Case Studies
  • Contact Us
  • Try Free demo
Select Page
ZAF###South Africa

Dec 30, 2017

ZAF###South Africa

Read More

MEX###Mexico

Dec 29, 2017

MEX###Mexico

Read More

ARG###Argentina

Dec 29, 2017

ARG###Argentina

Read More

BRA###Brazil

Dec 28, 2017

BRA###Brazil

Read More

IRN###Iran

Dec 28, 2017

IRN###Iran

Read More

«Back34567...Next»

Take The First Step Towards Medical Devices Registrations

Categories

Categories

  • Africa (35)
  • Asia (182)
    • Singapore (3)
  • Australia and Oceania (124)
  • Belgium (1)
  • Brazil (13)
  • Canada (49)
  • Case Study (19)
  • China (3)
  • COFEPRIS (1)
  • Consultant Post (7)
  • COVID-19 (33)
  • Denmark (1)
  • Ethiopia (27)
  • EU MDR/IVDR (117)
  • Europe (196)
  • FDA (409)
  • IMDRF (10)
  • India (4)
  • Indonesia (1)
  • IVD (2)
  • Japan (1)
  • Kazakhstan (9)
  • Malaysia (17)
  • MDCG (43)
  • Mexico (1)
  • MHRA (25)
  • North America (445)
  • Peru (2)
  • Philippines (2)
  • Poland (2)
  • RegDesk News/Info (27)
  • Russia (10)
  • Saudi Arabia (31)
  • Slovenia (1)
  • South America (28)
  • South Korea (2)
  • switzerland (10)
  • Taiwan (3)
  • TGA (80)
  • UK (14)
  • Uncategorized (327)
  • United States (329)

Tags

RegDesk (632)
medical devices (619)
FDA (495)
Medical Device (455)
guidance RegDesk (343)
guidance (329)
Medical Devices RegDesk (293)
united states (287)
United States of America (227)
North America (215)
FDA guidance (196)
regulation (160)
RegDes (157)
regulatory (155)
Food and Drug Administration (151)
medical device regulations (151)
fda medical devices (142)
mdr (138)
medical software (133)
TGA (116)
Asia (108)
Singapore (91)
hsa (88)
software (80)
South Asia (79)
regulations (78)
Southeast Asia (76)
guidances (71)
Europe (71)
Australia (67)
medical (62)
EU (61)
MDCG (58)
health canada (51)
COVID-19 (51)
Canada (49)
guidelines (49)
medical device grouping (45)
USA (45)
regdesk medical device (43)
medicines (42)
EU MDR (42)
TGA news (39)
mhra (35)
Austalia (35)
Australia Register of Therapeutic Goods (34)
European (33)
Questions (33)
Health Sciences Authority (31)
saudi arabia (31)
requirements (31)
sfda (30)
EC (28)
clinical (28)
Regulatory Authority (27)
Ethiopia (27)
Ethiopian FDA (27)
Ethiopian Food and Drug Authority (27)
uk (26)
medical device registration (26)
Tests (25)
Europe medical device regulations (24)
European Medical Device Regulations (24)
Medical Devices Ethiopia (23)
Malaysia (22)
Registration (22)
Clinical Trials (22)
IVDR (21)
Africa (20)
artg (20)
medical device software (20)
Brazil (20)
Labeling (20)
ivd (19)
EFDA (19)
Anvisa (19)
Cybersecurity (18)
SaMD (17)
Australian Register of Therapeutic Goods (16)
clinical trial (16)
classification (16)
changes (16)
regulatory affairs (15)
510k (15)
therapeutic goods administration (15)
Pharma (15)
European Commission (14)
notified bodies (14)
India (14)
Regulatory Legislation (14)
US (14)
UDI (14)
Quality (13)
China (13)
Regulatory News (13)
EMA (13)
Drugs (13)
manufacturers (13)
healthcare (13)
de novo (12)
IMDRF (12)
manufacturing (12)
devices (12)
russia (12)
submissions (12)
Coronavirus (12)
VMSR (11)
mda (11)
Medical Device Labeling (11)
Kazakhstan (11)
medical device authority malaysia (11)
Labelling (11)
Device (10)
International (10)
Pakistan (10)
AI Medical Devices (10)
European Union (10)
Tanzania (9)
swissmedic (9)
EU MDR and IVDR (9)
medical device advertising (9)
Saudi FDA (9)
Medical device marketing (9)
fda guidelines for medical devices (9)
medical device regulation (9)
clinical investigations (9)
Medical Device regulatory (9)
AI (9)
Photobiomodulation Devices (8)
personalized medical devices (8)
CDSCO (8)
EUA (8)
inspections (8)
human factors (8)
medical device labeling requirements (8)
medical device regulaions (8)
Pharmaceuticals (8)
CFDA (8)
ANVISA regulations (8)
Brazil medical devices (8)
ANVISA news (8)
brazil medical device classification (8)
medical device submissions (8)
regulatory requirements (8)
software as a medical device (8)
technology (8)
Switzerland (8)
surveillance (8)
Health Canada Guidance (8)
notification (7)
Recalls (7)
incident reporting (7)
Update (7)
medicine (7)
bahrain (7)
in vitro diagnostic (7)
Design Control (7)
virus (7)
AI Medical Software (7)
Big Data (7)
medical device coordination group (7)
TMDA (7)
Health Canada Guidelines (7)
reprocessing (7)
medical device regulations guidance (7)
advertising (7)
recall (7)
distribution (7)
Investigational Device Exemptions (7)
IDE (7)
3D printing medical devices (7)
clinical evaluation (7)
Clinical Studies (7)
post market surveillance (7)
ISO (7)
medical device guidance (7)
EU IVDR (7)
MedTech (7)
NDDA (7)
how to (6)
Saudi (6)
safer technologies program (6)
mutations (6)
quality system (6)
Digital (6)
Turkey (6)
Compliance (6)
Design (6)
risk (6)
cdrh (6)
advertising rules (6)
advertising regulations (6)
covid (6)
Japan (6)
asca (6)
conformity assessment (6)
Infusion Pumps (6)
ppe (6)
eudamed (6)
Big Data-Based Medical Devices (6)
Marketing (6)
combination products (6)
Unique Device Identification (6)
submission (6)
cybersecuirty (6)
adverse event reporting (6)
NHRA (6)
medical devices. regulations (6)
technologies (6)
biocompatibility (6)
Canada medical device regulations (6)
draft guidance (6)
pma (5)
label (5)
application (5)
Medical Device License (5)
brexit (5)
eCopy (5)
essential principles (5)
In vitro diagnostics (5)
Clinical Evidence (5)
roszdravnadzor (5)
medical device manufacturers (5)
Russian (5)
covid-19 tests (5)
510 (k) (5)
clinical guidelines (5)
quality system certification (5)
MDEL (5)
Medical Device Establishment License (5)
labels (5)
Reclassification (5)
distributor (5)
safety (5)
conformity assessment bodies (5)
implementation (5)
in vitro (5)
Austrlia (5)
510(k) submission (5)
De Novo Classification (5)
Custom-made medical devices (5)
medical device classification (5)
Medical Device Regulatory Consultants. Medical Device Approval | RegDesk
Subscribe to Our Newsletter
RegDesk, Inc.

2450 Holcombe Blvd, Suite X

Houston, TX 77021

desk@regdesk.co | +1 267 607 3375

Solutions
  • Application Builder
  • Regulatory Intelligence
  • Tracking
  • Regulatory Consulting
Resources
  • Device Regulation Library
  • Case Studies
Company
  • Beyond RIMS
  • Contact Us
  • Blog
  • HTML Sitemap

© 2023 RegDesk, Inc. All rights reserved

Request A Demo
Please fill out the form below and one of our team members will get back to you as soon as possible!



Request A Demo
Please fill out the form below and one of our team members will get back to you as soon as possible!