Last Updated on November 27, 2024 by The Health Master
Schedules – Medical Devices
Schedules – Medical Devices under Medical Devices Rules 2017
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: All types of Cosmetics
Schedules: All types of Medical Devices
Schedules: All types of Clinical Trials
Licensing procedure for Medical devices
Latest Notifications: Medical Devices
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