Inspection of overseas manufacturing site (1) On receipt of an application under sub ...

Shelf life of medical devices The shelf life of the medical devices, shall be determi ...

The Central Licensing Authority, may, after being satisfied with the information furn ...

REGISTRATION OF CERTAIN MEDICAL DEVICES 19A. (1) This Chapter shall be applicable to ...

Validity of registration A registration granted under sub-rule (3) of rule 83 in Form ...

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

Condition of permission to import or manufacture medical device which does not have i ...

All relevant clinical and non-clinical safety data will cover only the period of the ...