This chart lists the pharmaceutical, medical and related regulatory authorities of MENA regulations countries along with links to their relevant websites. 
Get to Know: MENA Regulations Authorities
Categories
Categories
- Africa (43)
- ANMAT (1)
- Argentina (1)
- Asia (219)
- Singapore (27)
- Australia (9)
- Australia and Oceania (130)
- Bahrain (1)
- Belgium (1)
- BfArM (11)
- Brazil (21)
- Canada (54)
- Case Study (6)
- CDRH (11)
- China (6)
- COFEPRIS (1)
- Consultant Post (7)
- COVID-19 (34)
- Czech Republic (1)
- Denmark (1)
- EDA (5)
- Egypt (5)
- Ethiopia (27)
- EU (2)
- EU MDR/IVDR (129)
- Europe (234)
- FDA (569)
- Germany (12)
- GMDN (1)
- Health Canada (3)
- Healthcare (2)
- HPRA (3)
- HSA (9)
- IMDRF (23)
- India (4)
- Indonesia (1)
- Ireland (3)
- ISO Standards (1)
- IVD (2)
- Japan (1)
- Kazakhstan (9)
- Latvia (1)
- Malaysia (20)
- MDA (1)
- MDCG (47)
- Medical Devices (2)
- Mexico (2)
- MHRA (48)
- NMPA (2)
- North America (456)
- orthopaedics (2)
- Peru (2)
- Philippines (3)
- Poland (2)
- RegDesk News/Info (25)
- Russia (10)
- Saudi Arabia (44)
- Slovenia (1)
- South America (28)
- South Korea (2)
- Southeast Asia (1)
- State Agency of Medicines of Latvia (1)
- Swissmedic (1)
- switzerland (21)
- Taiwan (3)
- TGA (94)
- Thailand (2)
- UK (37)
- Uncategorized (475)
- United Kingdom (2)
- United States (495)
Tags
medical devices (768)
RegDesk (758)
FDA (606)
Medical Device (532)
guidance RegDesk (433)
guidance (410)
Medical Devices RegDesk (363)
united states (304)
FDA guidance (272)
United States of America (243)
North America (225)
medical device regulations (211)
fda medical devices (184)
regulation (174)
Food and Drug Administration (167)
regulatory (166)
mdr (166)
RegDes (164)
medical software (144)
Asia (131)
TGA (126)
guidances (111)
Singapore (110)
hsa (109)
USA (97)
South Asia (95)
medical (95)
Southeast Asia (88)
Europe (86)
regulations (83)
software (81)
Australia (71)
EU (68)
MDCG (61)
regdesk medical device (61)
guidelines (59)
medical device registration (58)
mhra (55)
medical device grouping (55)
health canada (54)
medicines (52)
COVID-19 (51)
Canada (49)
Health Sciences Authority (49)
European (47)
modifications (46)
PCCP (46)
healthcare (45)
EU MDR (45)
TGA news (45)
saudi arabia (41)
Austalia (41)
Australia Register of Therapeutic Goods (40)
uk (39)
medical device regulation (39)
sfda (39)
Questions (39)
regulatory affairs (36)
Clinical Trials (36)
European Medical Device Regulations (36)
clinical (35)
SaMD (33)
requirements (31)
EC (30)
ivd (28)
Regulatory Approval (28)
Regulatory Authority (27)
Brazil (27)
Ethiopia (27)
Africa (27)
Ethiopian FDA (27)
Ethiopian Food and Drug Authority (27)
510k (26)
Anvisa (26)
Europe medical device regulations (26)
IMDRF (26)
Malaysia (25)
Tests (25)
USFDA (25)
clinical trial (23)
Medical Devices Ethiopia (23)
Registration (22)
cdrh (22)
Labeling (21)
IVDR (21)
MHRA Guidance (21)
artg (20)
medical device software (20)
swissmedic (19)
EFDA (19)
Saudi FDA (19)
Cybersecurity (18)
Switzerland (18)
Patient safety (18)
UDI (17)
AI Medical Devices (17)
classification (16)
medtech europe (16)
changes (16)
cybersecuirty (16)
Australian Register of Therapeutic Goods (16)
medical device regulaions (16)
Regulatory Compliance (16)
Quality (15)
Pharma (15)
Pakistan (15)
Drugs (15)
ANVISA regulations (15)
Brazil medical devices (15)
ANVISA news (15)
therapeutic goods administration (15)
USFDA Guidelines (15)
Regulatory Legislation (14)
US (14)
notified bodies (14)
mda (14)
European Commission (14)
India (13)
China (13)
Regulatory News (13)
EMA (13)
Digital Health (13)
manufacturers (13)
clinical investigations (13)
medical device authority malaysia (13)
russia (12)
European Union (12)
de novo (12)
manufacturing (12)
devices (12)
submissions (12)
Coronavirus (12)
Pre-Market Approval (12)
Kazakhstan (11)
bahrain (11)
MedTech (11)
Labelling (11)
legacy devices (11)
clinical evaluation (11)
Medical Device Labeling (11)
VMSR (11)
review clock (11)
Patient Rights (11)
Medical Ethics (11)
Device (10)
International (10)
fda guidelines for medical devices (10)
innovation (10)
Germany (10)
NHRA (10)
medical device regulations guidance (10)
healthcare technology (10)
EU IVDR (9)
EU MDR and IVDR (9)
artificial intelligence (9)
Medical Device regulatory (9)
AI (9)
Tanzania (9)
medical device advertising (9)
Medical device marketing (9)
IDE (9)
medical imaging devices (9)
United KingdomUK (9)
FDA approval (9)
CDSCO (8)
Turkey (8)
IVDs (8)
CFDA (8)
EUMDR (8)
brazil medical device classification (8)
regulatory requirements (8)
software as a medical device (8)
technology (8)
Health Canada Guidance (8)
monitoring (8)
quality system (8)
combination products (8)
medical device submissions (8)
EUA (8)
inspections (8)
surveillance (8)
personalized medical devices (8)
medical device labeling requirements (8)
medical device changes (8)
post market surveillance (8)
human factors (8)
sahpra (8)
Photobiomodulation Devices (8)
Establishment Licensing (8)
SFDA guidance (8)
Medical Device Improvement (8)
Egypt (7)
Pharmaceuticals (7)
Unique Device Identification (7)
ISO (7)
medical device classification (7)
3D printing medical devices (7)
medical device guidance (7)
medicine (7)
medical device coordination group (7)
advertising (7)
recall (7)
distribution (7)
510(k) submission (7)
virus (7)
reprocessing (7)
adverse event reporting (7)
NDDA (7)
notification (7)
Recalls (7)
incident reporting (7)
Update (7)
in vitro diagnostic (7)
exemption (7)
AI Medical Software (7)
Big Data (7)
TMDA (7)
Health Canada Guidelines (7)
Investigational Device Exemptions (7)
Clinical Studies (7)
Design Control (7)
21 CFR (7)
Saudi (6)
Compliance (6)
regulatory guidance (6)
Marketing (6)
Pharmacovigilance (6)
pma (6)
class 1 medical device (6)
machine learning (6)
Canada medical device regulations (6)
draft guidance (6)
FSCA (6)
BfArM (6)
risk (6)
asca (6)
conformity assessment (6)
eudamed (6)
drug device (6)
submission (6)
medical devices. regulations (6)
technologies (6)
implementation (6)
biocompatibility (6)
Digital (6)
covid (6)
ppe (6)
in vitro (6)
safer technologies program (6)
mutations (6)
Clinical Evidence (6)
advertising rules (6)
advertising regulations (6)
Big Data-Based Medical Devices (6)
resubmission (6)
how to (6)
Design (6)
Infusion Pumps (6)
De Novo Classification (6)
Medical Technology (6)
Fast Track Approval (6)
In vitro diagnostics (5)
Japan (5)
Thailand (5)
mexico (5)
brexit (5)
COFEPRIS (5)
medical device manufacturers (5)
Ireland (5)
class 3 medical device (5)
application (5)
clinical guidelines (5)
labels (5)
risk management (5)
label (5)
roszdravnadzor (5)
Russian (5)
covid-19 tests (5)
Reclassification (5)
safety (5)
conformity assessment bodies (5)
Custom-made medical devices (5)
eCopy (5)
essential principles (5)
510 (k) (5)
MDEL (5)
Medical Device Establishment License (5)
changes to existing devices (5)
alternatives (5)
510(k) notification (5)
MRDD (5)
Medical Device License (5)
Medical Device Recalls (5)
quality system certification (5)
distributor (5)
Austrlia (5)
Medical Device Compliance (5)
Pathology Peer Review (5)
x-ray (5)
x-ray imaging devices (5)
site master file preperation (5)
TGA Compliance (5)
Device Classification (5)
Australian Medical Devices: (5)
Clinical Research (5)
Fast-Track Process (5)
RegDesk (758)
FDA (606)
Medical Device (532)
guidance RegDesk (433)
guidance (410)
Medical Devices RegDesk (363)
united states (304)
FDA guidance (272)
United States of America (243)
North America (225)
medical device regulations (211)
fda medical devices (184)
regulation (174)
Food and Drug Administration (167)
regulatory (166)
mdr (166)
RegDes (164)
medical software (144)
Asia (131)
TGA (126)
guidances (111)
Singapore (110)
hsa (109)
USA (97)
South Asia (95)
medical (95)
Southeast Asia (88)
Europe (86)
regulations (83)
software (81)
Australia (71)
EU (68)
MDCG (61)
regdesk medical device (61)
guidelines (59)
medical device registration (58)
mhra (55)
medical device grouping (55)
health canada (54)
medicines (52)
COVID-19 (51)
Canada (49)
Health Sciences Authority (49)
European (47)
modifications (46)
PCCP (46)
healthcare (45)
EU MDR (45)
TGA news (45)
saudi arabia (41)
Austalia (41)
Australia Register of Therapeutic Goods (40)
uk (39)
medical device regulation (39)
sfda (39)
Questions (39)
regulatory affairs (36)
Clinical Trials (36)
European Medical Device Regulations (36)
clinical (35)
SaMD (33)
requirements (31)
EC (30)
ivd (28)
Regulatory Approval (28)
Regulatory Authority (27)
Brazil (27)
Ethiopia (27)
Africa (27)
Ethiopian FDA (27)
Ethiopian Food and Drug Authority (27)
510k (26)
Anvisa (26)
Europe medical device regulations (26)
IMDRF (26)
Malaysia (25)
Tests (25)
USFDA (25)
clinical trial (23)
Medical Devices Ethiopia (23)
Registration (22)
cdrh (22)
Labeling (21)
IVDR (21)
MHRA Guidance (21)
artg (20)
medical device software (20)
swissmedic (19)
EFDA (19)
Saudi FDA (19)
Cybersecurity (18)
Switzerland (18)
Patient safety (18)
UDI (17)
AI Medical Devices (17)
classification (16)
medtech europe (16)
changes (16)
cybersecuirty (16)
Australian Register of Therapeutic Goods (16)
medical device regulaions (16)
Regulatory Compliance (16)
Quality (15)
Pharma (15)
Pakistan (15)
Drugs (15)
ANVISA regulations (15)
Brazil medical devices (15)
ANVISA news (15)
therapeutic goods administration (15)
USFDA Guidelines (15)
Regulatory Legislation (14)
US (14)
notified bodies (14)
mda (14)
European Commission (14)
India (13)
China (13)
Regulatory News (13)
EMA (13)
Digital Health (13)
manufacturers (13)
clinical investigations (13)
medical device authority malaysia (13)
russia (12)
European Union (12)
de novo (12)
manufacturing (12)
devices (12)
submissions (12)
Coronavirus (12)
Pre-Market Approval (12)
Kazakhstan (11)
bahrain (11)
MedTech (11)
Labelling (11)
legacy devices (11)
clinical evaluation (11)
Medical Device Labeling (11)
VMSR (11)
review clock (11)
Patient Rights (11)
Medical Ethics (11)
Device (10)
International (10)
fda guidelines for medical devices (10)
innovation (10)
Germany (10)
NHRA (10)
medical device regulations guidance (10)
healthcare technology (10)
EU IVDR (9)
EU MDR and IVDR (9)
artificial intelligence (9)
Medical Device regulatory (9)
AI (9)
Tanzania (9)
medical device advertising (9)
Medical device marketing (9)
IDE (9)
medical imaging devices (9)
United KingdomUK (9)
FDA approval (9)
CDSCO (8)
Turkey (8)
IVDs (8)
CFDA (8)
EUMDR (8)
brazil medical device classification (8)
regulatory requirements (8)
software as a medical device (8)
technology (8)
Health Canada Guidance (8)
monitoring (8)
quality system (8)
combination products (8)
medical device submissions (8)
EUA (8)
inspections (8)
surveillance (8)
personalized medical devices (8)
medical device labeling requirements (8)
medical device changes (8)
post market surveillance (8)
human factors (8)
sahpra (8)
Photobiomodulation Devices (8)
Establishment Licensing (8)
SFDA guidance (8)
Medical Device Improvement (8)
Egypt (7)
Pharmaceuticals (7)
Unique Device Identification (7)
ISO (7)
medical device classification (7)
3D printing medical devices (7)
medical device guidance (7)
medicine (7)
medical device coordination group (7)
advertising (7)
recall (7)
distribution (7)
510(k) submission (7)
virus (7)
reprocessing (7)
adverse event reporting (7)
NDDA (7)
notification (7)
Recalls (7)
incident reporting (7)
Update (7)
in vitro diagnostic (7)
exemption (7)
AI Medical Software (7)
Big Data (7)
TMDA (7)
Health Canada Guidelines (7)
Investigational Device Exemptions (7)
Clinical Studies (7)
Design Control (7)
21 CFR (7)
Saudi (6)
Compliance (6)
regulatory guidance (6)
Marketing (6)
Pharmacovigilance (6)
pma (6)
class 1 medical device (6)
machine learning (6)
Canada medical device regulations (6)
draft guidance (6)
FSCA (6)
BfArM (6)
risk (6)
asca (6)
conformity assessment (6)
eudamed (6)
drug device (6)
submission (6)
medical devices. regulations (6)
technologies (6)
implementation (6)
biocompatibility (6)
Digital (6)
covid (6)
ppe (6)
in vitro (6)
safer technologies program (6)
mutations (6)
Clinical Evidence (6)
advertising rules (6)
advertising regulations (6)
Big Data-Based Medical Devices (6)
resubmission (6)
how to (6)
Design (6)
Infusion Pumps (6)
De Novo Classification (6)
Medical Technology (6)
Fast Track Approval (6)
In vitro diagnostics (5)
Japan (5)
Thailand (5)
mexico (5)
brexit (5)
COFEPRIS (5)
medical device manufacturers (5)
Ireland (5)
class 3 medical device (5)
application (5)
clinical guidelines (5)
labels (5)
risk management (5)
label (5)
roszdravnadzor (5)
Russian (5)
covid-19 tests (5)
Reclassification (5)
safety (5)
conformity assessment bodies (5)
Custom-made medical devices (5)
eCopy (5)
essential principles (5)
510 (k) (5)
MDEL (5)
Medical Device Establishment License (5)
changes to existing devices (5)
alternatives (5)
510(k) notification (5)
MRDD (5)
Medical Device License (5)
Medical Device Recalls (5)
quality system certification (5)
distributor (5)
Austrlia (5)
Medical Device Compliance (5)
Pathology Peer Review (5)
x-ray (5)
x-ray imaging devices (5)
site master file preperation (5)
TGA Compliance (5)
Device Classification (5)
Australian Medical Devices: (5)
Clinical Research (5)
Fast-Track Process (5)
