19F. Central Licensing Authority may verify the documents at any point of time and in ...

agents, contractors and sub-contractors, and clinical investigation sites shall be op ...

Studies: This section of PSUR shall capture the brief summary of clinically important ...

Recall detail Footnotes i Type of Product: Medicine, Medical Device, or Biological ii ...

(vii) the registration holder shall inform forthwith, any change of existing expert ...

Provided that, if the registration certificate holder fails to pay the required regis ...

22.0 Information required to be submitted for the in vitro diagnostic medical device: ...

Conditions for permission to conduct of clinical performance evaluation After grant ...