Directions and procedure for regularization of the examined FDC by the DTAB with respect to the approval process for manufacturers/stakeholders
Posted by: Hitesh Gupta July 6, 2022
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CDSCO
CDSCO
Amendment in Medical Device Rules, 2017
Posted by: Hitesh Gupta July 4, 2022
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- 4th July, 2022
Medical Devices (..Amendment) Rules, 2022 with insertion of Provision and Explanation to ISO 13485 certifi cation requirements.
Posted by: Hitesh Gupta February 28, 2022
Read MoreRegulation For CT Scan / MRI Equipment, All Implantable Devices etc. as Drugs which shall be operational
Posted by: Hitesh Gupta December 10, 2021
Read MoreThe regularization of 31 FDCs has been deemed rational, and drug makers have been given six months submit applications.
Posted by: Hitesh Gupta November 10, 2021
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