Format of informed consent form for Subjects participating in a clinical investigati ...

5. Sanitation: Availability of written specifications and procedures for cleaning the ...

4. Equipment: (i) brief description of major production and quality control laborato ...

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

an undertaking from the manufacturer stating that the proposed device is a Class A no ...

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

Sugam builds a comprehensive database of the various permissions and licenses issued ...

Amplified Maker Obligation (EPR) Is a administrative approach that holds producers ca ...