87B. Conditions of registration certificate to sell, stock, exhibit or offer for sal ...

(ii) Documents to be submitted with the application for grant of licence to manufactu ...

Appendix I CONTENTS OF A SITE OR PLANT MASTER FILE The manufacturer shall prepare a s ...

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

(3) In case of imported diagnostic in vitro diagnostic medical devices, the report of ...

THIRD SCHEDULE [Refer rules 13(5), 13(9), 14, 15, 20(4), 20(6)] DOCUMENTS REQUIRED FO ...

(v) details of competent technical staff, under whose direction and supervision the s ...

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