The Materiovigilance Programme of India (MvPI), under the Indian Pharmacopoeia Commission, has released the updated version of the medical devices adverse event reporting form, for the use of ...
MvPI releases draft IVD-MD adverse event reporting form, invites stakeholders' comments till March 5
The Materiovigilance Programme of India (MvPI), under the Indian Pharmacopoeia Commission (IPC), has released the draft in-vitro diagnostic medical device (IVD-MD) adverse event reporting form and has ...
The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) is bringing sweeping changes to the cosmetics industry. One such change requires a “responsible person” to maintain and submit certain ...
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