19D. (1) Any person who imports any medical device referred in rule 19A shall upload ...

Whereas the draft of the Medical Devices Rules, 2016 was published, as required under ...

4.0 Design and manufacturing information: 4.1 Device Design: The dossier should conta ...

REGISTRATION OF LABORATORY FOR CARRYING OUT TEST OR EVALUATION 81. Application for r ...

(C) devices notified from time to time under sub-clause (iv), of clause (b) of sectio ...

3. Definitions In these rules, unless the context otherwise requires, — (a) "academic ...

Medical devices requiring clinical investigation but claiming substantial equivalenc ...

Subjects (a) Inclusion criteria for subject selection. (b) Exclusion criteria for sub ...