Medical devices requiring clinical investigation but claiming substantial equivalenc ...

POST APPROVAL CHANGE (A) Changes in respect of following shall be considered as major ...

THE NATIONAL PHARMACEUTICAL PRICING AUTHORITY (NPPA) Is a regulatory body responsible ...

REGULATION OF MEDICAL DEVICE 4. Classification of medical devices (1) Medical devices ...

7.3.6 Design and development validation: Design and development validation shall be p ...

3.16 Rework means action taken on a non-conforming product that will fulfill the spec ...

THE NATIONAL PHARMACEUTICAL PRICING AUTHORITY (NPPA) Is a regulatory body responsibl ...

THE NATIONAL PHARMACEUTICAL PRICING AUTHORITY (NPPA) Is a regulatory body responsible ...