Blogs
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…
Consumer Health-USA and Asia Regulato…
USA
FDA Issues Draft Guidance on Registration and Listing of Cosmetic Product Facilities and Produ…
Medical Devices-Asia and ROW Regulato…
ASIA
INDIA (CDSCO)
India puts regulations that facilitate R&D at heart of new policy on pha…
The Role of Regulatory Tracking Softw…
In order to distribute the products, pharmaceutical manufacturers must ensure compliancy with global …
USFDA Latest Fee Summary Table for Dr…
Prescription Drug User Fee Amendments
FY 2023 and FY 2024 User Fee Rates
Fee CategoryFee Rates …
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