
Blogs

Consumer Health – USA/Europe/Asia/ROW…
USA
New Dietary Ingredient Notification Procedures and Timeframes: Guidance for Industry
FDA …

Consumer Health – USA/Europe/Asia/ROW…
USA
FSIS Guideline for Label Approval
This guideline is designed to help establishments deter…

Pharma/Biotech – USA, Europe, Asia an…
USA
Three FDA Final Guidance’s on Electronic Submission of Safety Reports
Three FDA final gui…

Adopting a Life Cycle Approach to Sof…
In March 2024, The document “Regulatory Guidance for Software Medical Devices – A Lifecycle Approach”…

Medical Devices – USA, Europe, Asia a…
USA
Accreditation Scheme for Conformity Assessment (ASCA)
The Center for Devices and Radiolog…

Pharma/Biotech – USA, Europe, Asia an…
USA
FDA Modernizes Informed Consent Guidance, Aligning With Common Rule Changes
The FDA has p…
Don’t miss out! Click here to stay in touch.
Categories
- Biopharma (52)
- Consumer Health (21)
- Cosmetics (11)
- Diagnostics (8)
- Digital Health (6)
- Food (1)
- Medical Device (107)
- OTC (5)
- Regulatory Intelligence (16)
- Standards (37)
Most used Tags
Asia Regulatory News (18)
BioTech (11)
Biotech Regulatory News (10)
Compliance (9)
Compliance Management (6)
Consumer Health (11)
EU Regulatory News (10)
Europe Regulatory News (12)
FDA (15)
FDA Updates (5)
Food Safety (7)
Global Compliance (8)
Global Health (9)
Healthcare Industry (6)
MDR (5)
Medical Device (5)
Medical Device Regulations (7)
Medical Devices (41)
MHRA (6)
Pharma (11)
Pharma Regulatory News (10)
Regulations (5)
Regulatory Affairs (11)
Regulatory Compliance (13)
Regulatory Intelligence (13)
Regulatory News (40)
Regulatory Updates (40)
ROW Regulatory News (15)
USA Regulatory News (21)
US FDA (8)
CONNECT WITH US

The First Step
Let's talk about how Vistaar can help you