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
- ACTD (1)
- Africa (43)
- ANMAT (1)
- Argentina (1)
- Asia (227)
- Singapore (35)
- Australia (24)
- Australia and Oceania (130)
- Bahrain (2)
- Belgium (1)
- BfArM (16)
- Brazil (21)
- Canada (63)
- Case Study (6)
- CDRH (11)
- China (6)
- CHMP (1)
- COFEPRIS (1)
- Consultant Post (7)
- COVID-19 (34)
- Czech Republic (1)
- Denmark (1)
- DRAP (10)
- DRCPFA (1)
- EDA (5)
- Egypt (5)
- Ethiopia (27)
- EU (21)
- EU MDR/IVDR (129)
- Europe (252)
- FDA (615)
- Germany (16)
- GMDN (1)
- Guatemala (1)
- Health Canada (12)
- Healthcare (2)
- HPRA (3)
- HSA (17)
- IMDRF (25)
- India (4)
- Indonesia (1)
- Ireland (3)
- ISO Standards (1)
- IVD (2)
- Japan (1)
- Kazakhstan (9)
- Latvia (1)
- Malaysia (26)
- MDA (7)
- MDCG (65)
- MDR (1)
- Medical Devices (2)
- Mexico (2)
- MHRA (48)
- NHRA (1)
- NMPA (2)
- North America (456)
- orthopaedics (2)
- Pakistan (10)
- Peru (2)
- Philippines (3)
- Poland (2)
- RegDesk News/Info (25)
- Russia (10)
- SAHPRA (4)
- Saudi Arabia (51)
- Serbia (1)
- SFDA (8)
- Slovenia (1)
- South Africa (5)
- South America (28)
- South Korea (2)
- Southeast Asia (1)
- State Agency of Medicines of Latvia (1)
- Swissmedic (1)
- switzerland (21)
- Taiwan (3)
- TGA (109)
- Thailand (2)
- Turkey (2)
- Turkish national regulating authority (1)
- Turkish Regulatory Authority (1)
- UK (37)
- Uncategorized (473)
- United Kingdom (2)
- United States (549)
- USA (3)
- USFDA (10)
Tags
medical devices (812)
RegDesk (758)
FDA (638)
Medical Device (535)
guidance RegDesk (433)
guidance (410)
Medical Devices RegDesk (363)
united states (324)
FDA guidance (294)
United States of America (243)
North America (225)
medical device regulations (212)
fda medical devices (184)
regulation (174)
mdr (171)
Food and Drug Administration (167)
regulatory (166)
RegDes (164)
medical software (144)
TGA (141)
Asia (131)
Singapore (118)
hsa (117)
guidances (111)
USA (101)
Europe (97)
South Asia (95)
medical (95)
Southeast Asia (88)
regulations (83)
software (82)
EU (80)
MDCG (80)
Australia (77)
health canada (63)
regdesk medical device (61)
guidelines (60)
medical device registration (58)
Canada (55)
mhra (55)
medical device grouping (55)
COVID-19 (52)
medicines (52)
Health Sciences Authority (49)
saudi arabia (48)
sfda (47)
European (47)
healthcare (46)
medical device regulation (46)
EU MDR (45)
TGA news (45)
modifications (45)
Austalia (45)
PCCP (45)
regulatory affairs (42)
Australia Register of Therapeutic Goods (40)
uk (39)
Questions (39)
Clinical Trials (36)
European Medical Device Regulations (36)
clinical (35)
510k (34)
ivd (34)
Regulatory Approval (34)
SaMD (33)
requirements (31)
Malaysia (30)
EC (30)
IMDRF (30)
Regulatory Authority (27)
Brazil (27)
Ethiopia (27)
Africa (27)
Ethiopian FDA (27)
Ethiopian Food and Drug Authority (27)
USFDA (27)
Regulatory Compliance (27)
Anvisa (26)
Europe medical device regulations (26)
Tests (25)
Labeling (24)
IVDR (24)
clinical trial (24)
cdrh (23)
artg (23)
Medical Devices Ethiopia (23)
Registration (22)
MHRA Guidance (21)
Cybersecurity (20)
medical device software (20)
Pakistan (19)
swissmedic (19)
mda (19)
EFDA (19)
Saudi FDA (19)
Patient safety (19)
Switzerland (18)
UDI (17)
classification (17)
AI Medical Devices (17)
Quality (16)
Digital Health (16)
European Union (16)
medtech europe (16)
changes (16)
cybersecuirty (16)
Australian Register of Therapeutic Goods (16)
medical device regulaions (16)
Pharma (15)
regulatory guidance (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)
European Commission (14)
clinical investigations (14)
Device Classification (14)
Clinical Research (14)
India (13)
China (13)
Regulatory News (13)
EMA (13)
manufacturers (13)
medical device authority malaysia (13)
clinical evaluation (13)
FDA approval (13)
russia (12)
de novo (12)
manufacturing (12)
devices (12)
combination products (12)
submissions (12)
Coronavirus (12)
Pre-Market Approval (12)
healthcare technology (12)
Kazakhstan (11)
bahrain (11)
MedTech (11)
Germany (11)
Labelling (11)
NHRA (11)
legacy devices (11)
Medical Device Labeling (11)
sahpra (11)
VMSR (11)
review clock (11)
Establishment Licensing (11)
Patient Rights (11)
Medical Ethics (11)
Device (10)
Turkey (10)
International (10)
Product Registration (10)
ISO (10)
medical device classification (10)
regulatory requirements (10)
fda guidelines for medical devices (10)
innovation (10)
BfArM (10)
conformity assessment (10)
medical device regulations guidance (10)
DRAP (10)
EU IVDR (9)
EU MDR and IVDR (9)
EUMDR (9)
artificial intelligence (9)
Medical Device regulatory (9)
AI (9)
Tanzania (9)
medical device advertising (9)
Medical device marketing (9)
Q-Submission (9)
IDE (9)
medical imaging devices (9)
United KingdomUK (9)
CDSCO (8)
IVDs (8)
CFDA (8)
brazil medical device classification (8)
software as a medical device (8)
technology (8)
Health Canada Guidance (8)
monitoring (8)
quality system (8)
eudamed (8)
medical device submissions (8)
EUA (8)
inspections (8)
surveillance (8)
personalized medical devices (8)
Clinical Evidence (8)
medical device labeling requirements (8)
medical device changes (8)
Clinical Studies (8)
post market surveillance (8)
human factors (8)
21 CFR (8)
Photobiomodulation Devices (8)
SFDA guidance (8)
Medical Device Improvement (8)
Egypt (7)
Compliance (7)
Pharmaceuticals (7)
Unique Device Identification (7)
pma (7)
3D printing medical devices (7)
medical device guidance (7)
medicine (7)
medical device coordination group (7)
risk management (7)
advertising (7)
recall (7)
distribution (7)
510(k) submission (7)
virus (7)
reprocessing (7)
adverse event reporting (7)
safety (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)
Design Control (7)
Product Recalls (7)
Saudi (6)
Marketing (6)
Pharmacovigilance (6)
class 1 medical device (6)
machine learning (6)
Canada medical device regulations (6)
draft guidance (6)
FSCA (6)
risk (6)
asca (6)
drug device (6)
submission (6)
medical devices. regulations (6)
technologies (6)
implementation (6)
biocompatibility (6)
third party review (6)
Digital (6)
covid (6)
ppe (6)
Reclassification (6)
in vitro (6)
safer technologies program (6)
mutations (6)
essential principles (6)
advertising rules (6)
advertising regulations (6)
Big Data-Based Medical Devices (6)
resubmission (6)
how to (6)
sterilization (6)
Design (6)
Infusion Pumps (6)
De Novo Classification (6)
clinical data (6)
Medical Technology (6)
Fast-Track Process (6)
Healthcare Innovation (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)
label (5)
roszdravnadzor (5)
Russian (5)
covid-19 tests (5)
conformity assessment bodies (5)
Custom-made medical devices (5)
Substantial Equivalence (5)
eCopy (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)
medical device manufacturing (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)
Australian Medical Devices: (5)
Fast Track Approval (5)
Adverse Events (5)
Clinical study (5)
Real World Evidence (5)
Therapeutic Goods (5)
RegDesk (758)
FDA (638)
Medical Device (535)
guidance RegDesk (433)
guidance (410)
Medical Devices RegDesk (363)
united states (324)
FDA guidance (294)
United States of America (243)
North America (225)
medical device regulations (212)
fda medical devices (184)
regulation (174)
mdr (171)
Food and Drug Administration (167)
regulatory (166)
RegDes (164)
medical software (144)
TGA (141)
Asia (131)
Singapore (118)
hsa (117)
guidances (111)
USA (101)
Europe (97)
South Asia (95)
medical (95)
Southeast Asia (88)
regulations (83)
software (82)
EU (80)
MDCG (80)
Australia (77)
health canada (63)
regdesk medical device (61)
guidelines (60)
medical device registration (58)
Canada (55)
mhra (55)
medical device grouping (55)
COVID-19 (52)
medicines (52)
Health Sciences Authority (49)
saudi arabia (48)
sfda (47)
European (47)
healthcare (46)
medical device regulation (46)
EU MDR (45)
TGA news (45)
modifications (45)
Austalia (45)
PCCP (45)
regulatory affairs (42)
Australia Register of Therapeutic Goods (40)
uk (39)
Questions (39)
Clinical Trials (36)
European Medical Device Regulations (36)
clinical (35)
510k (34)
ivd (34)
Regulatory Approval (34)
SaMD (33)
requirements (31)
Malaysia (30)
EC (30)
IMDRF (30)
Regulatory Authority (27)
Brazil (27)
Ethiopia (27)
Africa (27)
Ethiopian FDA (27)
Ethiopian Food and Drug Authority (27)
USFDA (27)
Regulatory Compliance (27)
Anvisa (26)
Europe medical device regulations (26)
Tests (25)
Labeling (24)
IVDR (24)
clinical trial (24)
cdrh (23)
artg (23)
Medical Devices Ethiopia (23)
Registration (22)
MHRA Guidance (21)
Cybersecurity (20)
medical device software (20)
Pakistan (19)
swissmedic (19)
mda (19)
EFDA (19)
Saudi FDA (19)
Patient safety (19)
Switzerland (18)
UDI (17)
classification (17)
AI Medical Devices (17)
Quality (16)
Digital Health (16)
European Union (16)
medtech europe (16)
changes (16)
cybersecuirty (16)
Australian Register of Therapeutic Goods (16)
medical device regulaions (16)
Pharma (15)
regulatory guidance (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)
European Commission (14)
clinical investigations (14)
Device Classification (14)
Clinical Research (14)
India (13)
China (13)
Regulatory News (13)
EMA (13)
manufacturers (13)
medical device authority malaysia (13)
clinical evaluation (13)
FDA approval (13)
russia (12)
de novo (12)
manufacturing (12)
devices (12)
combination products (12)
submissions (12)
Coronavirus (12)
Pre-Market Approval (12)
healthcare technology (12)
Kazakhstan (11)
bahrain (11)
MedTech (11)
Germany (11)
Labelling (11)
NHRA (11)
legacy devices (11)
Medical Device Labeling (11)
sahpra (11)
VMSR (11)
review clock (11)
Establishment Licensing (11)
Patient Rights (11)
Medical Ethics (11)
Device (10)
Turkey (10)
International (10)
Product Registration (10)
ISO (10)
medical device classification (10)
regulatory requirements (10)
fda guidelines for medical devices (10)
innovation (10)
BfArM (10)
conformity assessment (10)
medical device regulations guidance (10)
DRAP (10)
EU IVDR (9)
EU MDR and IVDR (9)
EUMDR (9)
artificial intelligence (9)
Medical Device regulatory (9)
AI (9)
Tanzania (9)
medical device advertising (9)
Medical device marketing (9)
Q-Submission (9)
IDE (9)
medical imaging devices (9)
United KingdomUK (9)
CDSCO (8)
IVDs (8)
CFDA (8)
brazil medical device classification (8)
software as a medical device (8)
technology (8)
Health Canada Guidance (8)
monitoring (8)
quality system (8)
eudamed (8)
medical device submissions (8)
EUA (8)
inspections (8)
surveillance (8)
personalized medical devices (8)
Clinical Evidence (8)
medical device labeling requirements (8)
medical device changes (8)
Clinical Studies (8)
post market surveillance (8)
human factors (8)
21 CFR (8)
Photobiomodulation Devices (8)
SFDA guidance (8)
Medical Device Improvement (8)
Egypt (7)
Compliance (7)
Pharmaceuticals (7)
Unique Device Identification (7)
pma (7)
3D printing medical devices (7)
medical device guidance (7)
medicine (7)
medical device coordination group (7)
risk management (7)
advertising (7)
recall (7)
distribution (7)
510(k) submission (7)
virus (7)
reprocessing (7)
adverse event reporting (7)
safety (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)
Design Control (7)
Product Recalls (7)
Saudi (6)
Marketing (6)
Pharmacovigilance (6)
class 1 medical device (6)
machine learning (6)
Canada medical device regulations (6)
draft guidance (6)
FSCA (6)
risk (6)
asca (6)
drug device (6)
submission (6)
medical devices. regulations (6)
technologies (6)
implementation (6)
biocompatibility (6)
third party review (6)
Digital (6)
covid (6)
ppe (6)
Reclassification (6)
in vitro (6)
safer technologies program (6)
mutations (6)
essential principles (6)
advertising rules (6)
advertising regulations (6)
Big Data-Based Medical Devices (6)
resubmission (6)
how to (6)
sterilization (6)
Design (6)
Infusion Pumps (6)
De Novo Classification (6)
clinical data (6)
Medical Technology (6)
Fast-Track Process (6)
Healthcare Innovation (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)
label (5)
roszdravnadzor (5)
Russian (5)
covid-19 tests (5)
conformity assessment bodies (5)
Custom-made medical devices (5)
Substantial Equivalence (5)
eCopy (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)
medical device manufacturing (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)
Australian Medical Devices: (5)
Fast Track Approval (5)
Adverse Events (5)
Clinical study (5)
Real World Evidence (5)
Therapeutic Goods (5)
