Welcome to Association of Medical Device Industry which allows the Govt. and all stakeholders of Healthcare to access a single point of contact and a one common platform to address the needs & growth of Indian Medical Device Industry and work to create India as the Preferred Manufacturing Destination and Global Supply Source.

Comments invited for

VISION PRESENTATION

“Proposed draft bill (IMDA) on Medical Device Regulation through Ministry of Science and Technology” – by Dr. G.S. Bhuvaneshwar

Please submit comments on “Proposed Export Guideline Note to DCGI”

Please submit comments on “Procedure for Issuing FSC – Dt. 26.02.09”

FSC – DGFT Revised Notification – Public Notice No.137 Dt. 19.01.09

Please submit comments on “Draft of Schedule M-III with Annexures

PROPOSED DRAFT GUIDELINES FOR THE REGULATORS FOR ASSESSMENT OF A MEDICAL DEVICE MANUFACTURING ORGANIZATION

EPSP-ANNEXURE I

ANNEXURE II - DOCUMENTS REQUIRED FOR A TECHNICAL FILE

ANNEXURE – III (Product Design Dossier)

EXAMPLE -EPSP REPORT -IV CANNULAS

RISK ANALYSIS- I V CANNULA