Blogs
Pharma/Biotech – USA, Europe, Asia an…
USA
FDA Modernizes Informed Consent Guidance, Aligning With Common Rule Changes
The FDA has p…
Consumer Health – USA/Europe/As…
USA
New Directory of Ingredients Used in Products Marketed as Dietary Supplements
The U.S. Food…
Medical Devices – Europe, Asia…
EUROPE
Expression of interest open – Possible second call for EU reference laboratories for high…
New Developments in Treatment of Rare…
Rare diseases are a complex of over 5000 pathologies representing 10% of the entire human pathology. …
Consumer Health USA/Asia/ROW Regulato…
USA
FDA announces availability of Additional Submission Tools for Cosmetic Facility Registration a…
USA/Europe BioPharma Regulatory 2023 …
AUSTRIA
User Manual for Marketing Authorisation and Lifecycle Management of Medicines
BASG p…
Don’t miss out! Click here to stay in touch.
Categories
- Biopharma (53)
- Consumer Health (15)
- Cosmetics (8)
- Diagnostics (6)
- Digital Health (6)
- Food (1)
- Medical Device (98)
- OTC (3)
- Regulatory Intelligence (5)
- Standards (34)
Most used Tags
Asia Regulatory News (18)
BioTech (10)
Biotech Regulatory News (10)
Compliance (8)
Compliance Management (5)
Consumer Health (8)
EU Regulatory News (10)
Europe Regulatory News (12)
FDA (9)
FDA Updates (5)
Global Compliance (7)
Global Health (6)
Healthcare Industry (6)
IVDR (5)
MDR (5)
medical device labeling requirements (5)
Medical Devices (39)
MHRA (6)
Pharma (11)
Pharma Regulatory News (10)
Regulations (5)
Regulatory Affairs (6)
Regulatory Compliance (9)
Regulatory Intelligence (12)
Regulatory News (36)
Regulatory Updates (34)
ROW Regulatory News (15)
Swissmedic (5)
USA Regulatory News (21)
US FDA (8)