Page 1 of 4 Version : 1.2 MEDICAL DEVICE ADVERSE EVENT REPORTING FORM Materiovigilance Program of India (MvPI) This form is intended to collect information on Medical Devices Adverse Event…
Page 1 of 4 Version : 1.2 MEDICAL DEVICE ADVERSE EVENT REPORTING FORM Materiovigilance Program of India (MvPI) This form is intended to collect information on Medical Devices Adverse Event…
Admin-80()/6/2024-eoffice |/2827/2024F.No. 80(4)/6/2024-eoffice (E-8800)भारत GxHR/Government of Indiaस्वास्थ्य और परिवार कल्याण मंत्रालय/भांग्रांडए of Health and Family WelfareTaReg ai Feleenea/Directorate General of Health Servicesmala ssf ama faa ds4/Central Drugs Standard Control Organisation(HQ)FDA…
List of Drugs, Medical Devices, Vaccine and Cosmetics declared as Spurious for the Month of September – 2024 As part of the continuous regulatory surveillance, drugs samples are picked from…
