TANZANIA MEDICINES AND MEDICAL DEVICES AUTHORITY

ISO 9001: 2015 CERTIFIED

PUBLIC NOTICE

25^th November, 2020

SUBMISSION OF PRODUCT SAMPLES ALONG WITH APPLICATIONS FOR REGISTRATION AND RE-REGISTRATION OF MEDICINAL PRODUCTS

1. TMDA wishes to inform all applicants that, pursuant to sub regulation 5(1) of the Tanzania Medicines and Medical Devices (Registration of Medicinal Products) Regulations, 2015 and in accordance with the current guidelines; submission of product samples along with application for registration is a requirement.
2. In view of this, all applicants are reminded to always submit sufficient number of samples immediately after lodging their application through the online portal.
3. Lastly, it should be noted that processing of applications shall commence only after submission of product samples. In the event that samples cannot be provided, applicant should request prior approval from TMDA.