CDSCO has come up with a presentation to support device industry for a common Non-Compliances observed during review of Applications for Registration and Import Licenses of Medical Devices.

This is yet another step which indicates the support of CDSCO to Industry.  Devices companies and CRO who are conducting clinical studies in Devices should have a look in the attached presentation prepared by CDSCO. 

This will enable companies to plan and manage their submission as expected by CDSCO.

Non-compliances-Applications-Registration-&-Import(1)

Non-compliances Observed During Review of Applications for Registration and Import Licences of Medical Devices

Leave a Reply

Your email address will not be published. Required fields are marked *

Visit Us On TwitterVisit Us On Google PlusVisit Us On LinkedinVisit Us On Facebook