Other information: This section of PSUR shall include details about signals and Risk ...

Post Marketing Surveillance: (i) Subsequent to approval of an Investigational medical ...

ERP License in India-- Mandatory Requirements for Medical Device Reporting (MDR) Med ...

Discussion and overall conclusions The conclusions may include the following points:— ...

(v) "intended use" means the use for which the medical device is intended according t ...

(iv) the person holding registration certificate shall maintain records of tests for ...

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

7.3.2 Design and development inputs: Inputs relating to product requirements shall be ...