Electronic Regulatory Information System (eRIS)

eRIS is the umbrella system at EFDA comprised of sub-systems which work together:

• i-License which allows entities to apply for certificate of competency to register and import products.
• i-Register which used to manage the medicine registration process when an applicant seeks to register a pharmaceutical in Ethiopia for later import.
• i-Import which used to manage the import process, once registered in Ethiopia.
• i-Verify which is used to verify and check the legality and authorization status of medicines by EFDA and monitor the movement of medicines from manufacturer to the point of issue.