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Viksit Bharat Viksit Goa
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Viksit Bharat Viksit Goa
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Viksit Bharat Viksit Goa
Latest News:
Regulatory requirements for outsourcing sterilization activity of medical devices by a manufacturer under Medical Device Rules, 2017 (CIRCULARS)DCGI directs drugs manufacturers to file safety & efficacy data on non-approved FDC formulation before 31st August 2013 (NOTIFICATIONS)Appointment of Registering Authority (NOTIFICATIONS)
Consumer Awareness
Food safety Mitra – Friend of Food Safety
Novel Coronavirus (Covid-19)
FSSAI guidance note on plastic eggs
FSSAI advisory on Formalin
Brouchure on Project Safe & Nutritious Food in Goa
Initiatives by FDA Goa on Safe & Nutritious Food
DART Spot Adulteration of Food Items
Handy Guide to Safe Use of Medicines
Novel Coronavirus (Covid-19)
FSSAI guidance note on plastic eggs
FSSAI advisory on Formalin
Brouchure on Project Safe & Nutritious Food in Goa
Initiatives by FDA Goa on Safe & Nutritious Food
DART Spot Adulteration of Food Items
Handy Guide to Safe Use of Medicines
ROLE OF FDA
WELCOME TO OUR WEBSITE
The Directorate of Food and Drugs Administration, Government of Goa was established in November’ 1991 with its office functioning from the building premises at Campal, Panaji – Goa. Thereafter the office premises was shifted and functioned from the Old Goa Medical Complex at Panaji – Goa; until October 2003 and thereafter the Directorate functioned from the Old IPHB Complex at Altinho, Panaji – Goa until February 2014.
NEWS IN FOCUS
- Seeking Expression of Interest for Analysis of Food Articles
- Monitoring activities of temporary food businesses esp. during festivities seasonal events
- Registration Online National Drug Licensing System-Retail_wholesale firms
- Grant of blood centre licenses through ONDLS portal
- Grant of Blood centre licence through ONDLS portal
- Validity of FSSAI recognised Food Testing Laboratories
- 14 FDC prohibited to manufacture for sale, sale and distribution for human use
CIRCULARS,ORDERS & NOTIFICATIONS
- Regulatory requirements for outsourcing sterilization activity of medical devices by a manufacturer under Medical Device Rules, 2017 (CIRCULARS)
- DCGI directs drugs manufacturers to file safety & efficacy data on non-approved FDC formulation before 31st August 2013 (NOTIFICATIONS)
- Appointment of Registering Authority (NOTIFICATIONS)
- Immediate withdrawal of the permission to manufacture all combinations of Tapentadol and all combinations of Caresoprodol (CIRCULARS)