Medical Device Contract Manufacturing
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Medical Device Registration in Greece
Entering Greece market offers tremendous opportunities by medical device companies, but it is not without challenges.
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New notification by DCGI
Whereas a draft of certain rules further to amend the Medical Devices Rules, 2017 was published as required under sub-section (1) of section 12 and sub-section (1) of section 33 of the Drugs and Cosmetics Act, 1940 (23 of 1940) vide notification of the Government of India in the Ministry of Health and Family Welfare (Department of Health and Family Welfare)
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Medical Device Validation Master Plan (VMP)
A validation master plan (VMP) diagrams the standards associated with the capability of an office, characterizing the areas and systems to be approved, and gives a composed program for achieving and keeping up a certified facility.
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