How to operate an Online System for Medical Device CDSCO|Medical Device Registration in India:L-2

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How to operate an Online System for Medical Device CDSCO|Medical Device Registeration in India:L-2@ivdmanufacturing7208

Online Portal for Medical devices enables applicant to submit online applications for Medical Devices regulatory process to CDSCO. It will also enable upload of supporting documents, respond to queries from CDSCO officials and track their application status. The user account lists out all the applications submitted and licenses/permissions held by them and provides the statistical analysis of the applications for various processes & licenses issued, suspended /cancelled, withdrawn.

MDR-2017 (Medical Device Regulation)

List of Queries -
Medical Device Registration in India
How to add address
How to edit address
how to add site address
IVD Registration in India
CDSCO Registration in India
How to register Medical Device in India
what is the Registeration process of CDSCO in India
What is the Registeration process of Medical Device in India
Register your Medical Device in CDSCO India
What is Online System for Medical Device CDSCO
What is the benefits of Online System for Medical Device CDSCO
Online System for Medical Device CDSCO kya hota hai ?
Online System for Medical Device CDSCO kya hai ?
Online System for Medical Device CDSCO Guidelines ?
Classification of medical devices
Medical device grouping
Medical Device Registration In India | CDSCO guidelinesREGISTRATION OF CLASS A (NON-STERILE AND NONMEASURING) MEDICAL DEVICES
MANUFACTURE OF MEDICAL DEVICES FOR SALE OR FOR DISTRIBUTION
Application for manufacture for sale or for distribution of Class A 12
[(other than non-sterile and non-measuring)] or Class B medical device
Application for manufacturing Class C or Class D devices
Requirements for grant of manufacturing licence or loan licence
Test licence to manufacture for test, evaluation, clinical investigations,
Application for grant of import licence
The manufacturer of a medical device shall upload the information
specified in sub-rule (2) relating to that medical device for registration on the
"Online System for Medical Devices" established by the Central Drugs
Standard Control Organisation for this purpose.


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