Blogs
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…
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…
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