https://www.acplgroupindia.in
91

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

View more

2. Bio-compatibility tests data, Report of bio-compatibility tests along with rationale fo...

View more

21.0 Post marketing surveillance data (vigilance reporting): The dossier should contain th...

View more

Obtaining a regulatory license often involves an application process, fees, background che...

View more

Proposed instructions for use or electronic instructions for use and labels.] (b) Data to ...

View more

Note: 1. All the test reports submitted as a part of the dossier should be signed and date...

View more

22.0 Information required to be submitted for the in vitro diagnostic medical device: (1) ...

View more

7.5.4 Customer property: The manufacturer shall exercise care with customer property while...

View more

Examined periodically, at least once a year. Records shall be maintained thereof. 6.2.2 Co...

View more

Subscribe for latest offers and updates.

we hate spam too