The device master file should include the following device descriptive information:— ...

Description and specification, including variants and accessories of the in vitro dia ...

Short title and commencement (1) These rules may be called the Medical Devices Rules, ...

(b) the intended user (lay person or professional); (c) a general description of the ...

Definitions In these rules, unless the context otherwise requires, — (a) "academic cl ...

EPR Plastic Waste Registration Near Me -- Is a administrative approach that holds pr ...

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

EXTENDED PRODUCER RESPONSIBILITY (EPR) Is a regulatory approach that holds manufactu ...