CDSCO had organized a meeting with the stakeholders to discuss the issues relating to indigenous manufacturing of medical devices. Several documents including revised Checklist for Pre Screening for acceptability of Applications, FAQ’s for medical devices and IVD, Guidance documents for grant of license and revised Schedule MII were discussed during the meeting.

From Amcham, the meeting was attended by Mr. Kulveen Bali, Manager-Regulatory and Quality, 3M and Mr. Asok Kumar, VP-RA/QA, Johnson and Johnson and Mr. Gaurav Mendiratta, Sector Manager-Medical Devices, Amcham.