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Posted On: Jul 02, 2020

TANZANIA MEDICINES AND MEDICAL DEVICES AUTHORITY

ISO 9001: 2015 CERTIFIED

PUBLIC NOTICE

30th June, 2020

ONLINE SYSTEM FOR SUBMISSION OF APPLICATIONS FOR REGISTRATION OF PRODUCTS, PREMISES, CLINICAL TRIALS AND GOOD MANUFACTURING PRACTICES (GMP) INSPECTIONS

  1. The TMDA wishes to inform its esteemed customers and the general public that it has introduced online submission system of applications for registration of products, premises, clinical trials and Good Manufacturing Practice (GMP)
  2. In this regard, applicants submitting applications for registration of products (new, renewal and variation), premises, clinical trials and GMP with effective from 1st of July, 2020 are requested to submit their applications through the online portal. Applicants or Local Technical Representatives (LTRs) may register in the system and obtain the credentials to get access to the system through this link https://imis2.tmda.go.tz/portal.
  3. You are kindly requested to follow the instructions provided on the portal. In case of difficulties in following up the instructions, you may contact the following TMDA staff for support:-
    Fabian Lwanole [Phone: +255 762 533 530, Email: fabian.lwanole@tmda.go.tz]
    Salehe Mwenyevyale [Phone: +255 753 747 474, Email: salehe.mwenyevyale@tmda.go.tz]
    Masuke Ng’habi [ Phone: +255 738 777 870, Email: masuke.nghabi@tmda.go.tz]
    Sadam Kyamani [Phone: +255 783 992 449 , Email: sadam.kyamani@tmda.go.tz]
    Office Email: mis@tmda.go.tz
  4. We thank you for your continued cooperation.
Issued by:
Acting Director General,
Tanzania Medicines and Medical Devices Authority (TMDA),
PSSSF Building, Makole
P. O. Box 1253, Dodoma Or
P. O. Box 77150, Dar es Salaam
Phone: +255 22 2452108/2450512/2450751
Fax: +255 22 2450793
Hotline: 0800110084