Schedules: Medical Devices

Last Updated on June 15, 2021 by The Health Master

Schedules – Medical Devices

Schedules – Medical Devices under Medical Devices Rules 2017

Rules Law
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As per Medical Devices Rules 2017 we have provided all the Schedules introduced in these rules, Click below links for more information:

First Schedule – Parameters for classification of medical devices and in vitro diagnostic medical devices

Second Schedule – Fee payable for licence, permission and registration certificate

Third Schedule – Documents required for registration of Notified Body, its duties and functions.

Fourth Schedule – Documents required for grant of licence to manufacture for sale or for distribution or import

Fifth Schedule – (QMS) Quality Management System for medical devices and in vitro diagnostic medical devices

Sixth Schedule – Post approval change

Seventh Schedule – Requirements for permission to import or manufacture investigational medical device for conducting clinical investigation

Eight Schedule – Exemptions

Schedules: Drugs

Schedules: Cosmetics

Schedules: Clinical Trials

Licensing procedure for Medical devices

Latest Notifications: Medical Devices

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