Blogs
Medical Devices-Asia and ROW Regulato…
ASIA
INDIA
The Indian Regulatory Authority (CDSCO) has released List of medical devices testing…
Understanding FDA Labeling Regulations
All labels and other written, printed or graphic matter upon any article or any of its containers or …
Role of Technology in Regulatory Inte…
Regulatory intelligence is a systematic process of collecting, analyzing, and disseminating informati…
Pharma/Biotech – USA, Europe Re…
USA
FDA Draft Guidance Pushes for Development of Stimulant Use Disorder Treatments
With no FDA …
Medical Devices-USA/Europe Regulatory…
USA
Electronic Submission Template for Medical Device 510(k) Submissions
The FDA Electronic sub…
Revised GMP guidelines for Pharma in …
The government recently directed all pharmaceutical companies in the country to implement the revised…
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