FDA ePermit Upgrade 12th December 2016

  • DATE07 Dec 2016

Upgrade eMDA System: Food and Drug Authority e-Permit

In order to support the developing needs of the Food and Drug Authority (FDA) the e-Permit issued through the eMDA platform has been upgraded.

The FDA e-Permit has been upgraded in order to capture detailed information on medicines that are imported into Ghana, specifically:
The product name
The molecule name, or INN (International Non-proprietary Name)
The EphMRA (European Pharmaceutical Market Research Association) classification code
The NFC (New Form Codes)

FDA Applicants using the eMDA system will be required to enter a unique FDA registration number issued at the time of drug registration, this will link to the drugs specific attributes and enable FDA to improve the efficiency of effectiveness of its compliance checks.

Enquiries may be addressed to:
Eben Engmann
Deputy Manager, TradeNet
Ghana Community Network Services Limited (GCNet)
0244 037457