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Tanzania Food and Drugs Authority (TFDA) is a regulatory body under the Ministry of Health and Social Welfare which is responsible for regulating the quality and safety of food, drugs, cosmetics and medical devices. more about TFDA
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Now you can register your Clinical Trial ( i.e. Protocol Registration ) online through the Tanzania Clinical Trial Registry (TzCTR) system.
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Have you suffered an adverse drug reaction? If so please consult your healthcare provider to fill the ADR form on-line. or  download the form, have it filled by your healthcare provider and send it to us.
[more about Adverse Drug Reaction]
The authority provides education to the public about food, drugs, cosmetics and medical devices. For more information   Click here  
 
     
More Press Release
  1. Announcement to Importers and Exporters of Pharmaceuticals and Raw Materials.
    (Posted: 01 August, 2011)

  2. Tamko la Rasilimali na Madeni Zinazotakiwa Kujazwa na Viongozi wa Umma.
    (Imetolewa: 21 July, 2011)

  3. a) Tangazo kwa Wafanyabiashara wa Chakula, Dawa, Vipodozi na Vifaa Tiba Kuhusu Kuhuisha Vibali vya Kuendesha Biashara za Chakula, Dawa, Vipodozi na Vifaa Tiba.
    (Imetolewa: 20 Juni, 2011)

    b) Renewal of Business Permit for Food, Drugs, Cosmetics and Medical Devices Businesses.
    (Posted: 20th June, 2011)

  4. a) Announcement to Manufacturers and Dealers of Medical Devices.

    b)The Authority wishes to inform its esteemed stakeholders that 1st phase of registration of medical devices commenced on 1st January, 2010. Based on the evaluation of applications received, 11 medical device products have been registered in February, 2011.

    Here is a List of Medical Devices Registered in February, 2011.
    (Posted: 28th March, 2011)

  5. Ufafanuzi Kuhusu Ubora wa Dawa za Malaria hapa nchini.
    (Imetolewa: 9 Machi, 2011)

  6. a) Temperary Suspension of Manufacturing, Importation, Distribution, Sale and Use of Sub-Standard Medicines.
    (Posted: 17th January, 2011)

    b) Kusitisha kwa Muda Utengenezaji, Uingizaji, Usambazaji na Matumizi ya Dawa zenye Viwango Duni vya Ubora.
    (Imetolewa: 17 Januari, 2011)

  7. The Authority calls upon all people engaged in the sale or distribution of modified traditional medicines manufactured in the country to notify their products to the Authority within 12 months from the date of this notice.
    (Posted: 15th December, 2010)

  8. Requirements on Importation of Syringes into Tanzania.
    (Posted: 2nd November, 2010)

  9. Wajumbe wa Bodi ya Ushauri ya Wizara kwa Mamlaka ya Chakula na Dawa (TFDA).
    (Imetolewa: 20 Oktoba, 2010)

  10. Maelezo ya Utangulizi ya Kaimu Mkurugenzi Mkuu wa Mamlaka ya Chakula na Dawa (TFDA), Hiiti B. Sillo Wakati wa Semina ya Uhamasishaji Wadau wa TFDA Kutka MOAT, TABOA na Wahariri Watendaji wa Vyombo vya Habari, Kuhusu Udhibiti wa Matangazo ya Bidhaa katika Ukumbi wa Mamlaka, Tarehe 19 Oktoba, 2010.
    (Imetolewa: 19 Oktoba, 2010 )

  11. Kuondoa Amri ya Kusitisha kwa Muda Uingizaji, Usambazaji, Uuzaji na Matumizi ya Maziwa ya NAN 2 Yaliyosajiliwa.
    (Imetolewa: 7 Oktoba, 2010)

  12. Opening Remarks by Mr. Hiiti B. Sillo, Acting Director General of Tanzania Food and Drugs Authority (TFDA) During the Training in Analysis of Pesticide Residues in Food Stuffs at TFDA Conference Hall, Dar es Salaam, 13 Septemba 2010.
    (Posted: 13th September, 2010)

  13. Kuruhusu Uagizaji, Usambazaji, Uuzaji na Matumizi ya Dawa ya Kutibu Malaria ya Vidonge ya Metakelfin Kutoka Kampuni ya Pfizer Inc. N/Y Inayotengenezwa na Kiwanda cha Dawa cha Pharmacia & Upjohn cha Italia .
    (Imetolewa: 1 Septemba, 2010)

  14. a) Maelezo ya Utangulizi ya Kaimu Mkurugenzi Mkuu wa TFDA, Bw. Hiiti B. Sillo Katika Mkutano wa Waandishi wa Habari Kuhusu Matokeo ya Operesheni Mamba III Katika Ukumbi wa Mamlaka ya Chakula Na Dawa, Tarehe 26 Agosti 2010.

    b) Taarifa kwa Umma Kuhusu Matokeo ya Operesheni Mamba Awamu ya Tatu Itakayotolewa Na Mkurugenzi wa Upelelezi wa Makosa ya Jinai Kamishna wa Polisi Robert Manumba Katika Ukumbi wa Mamlaka ya Chakula na Dawa Tarehe 26 Agosti 2010.
    (Imetolewa: 26 Agosti, 2010 )

  15. Taarifa kwa Umma Kuhusu Kuwepo katika soko Vyakula ambavyo ni Bandia au ambavyo Havijasajiliwa
    (Imetolewa: 13 Agosti, 2010 )

  16. Kusitisha na kudhibiti matumizi ya sindano za kawaida (Standard Disposable Syringes) na kuimarisha matumizi ya
    Sindano zinazojiharibu baada ya matumizi (Autodisable Syringes)
    (Imetolewa: 6 Mei, 2010 )

  17. Phasing Out and Limiting use of Standard Disposable Syringes in favour of Autodisable Syringes
    (Posted: 22nd April, 2010 )

  18. Huishwaji wa Vibali vya viwanda vya kusindika/kutengeneza vyakula kwa mwaka 2010/2011
    (Imetolewa: 1 Aprili, 2010 )

  19. Renewal of Business Permit for Local Food Processors Manufacturers for the year 2010/2011
    (Posted: 1st April, 2010 )

     
 
 
 
  1. Mkutano wa Wamiliki wa Maduka ya Dawa Baridi Mkoani Dar es Salaam, tarehe 17 January 2012.
    (Posted: 16th January, 2012)

  2. Announcement to all Parties Conducting Clinical Trials and those Providing Preventive Chemotherapy in Tanzania.
    (Posted: 30th December, 2011)

  3. Clarification on Inspection of Overseas Pharmaceutical Manufacturing Facilities by TFDA.
    (Posted: 21st December, 2011)

  4. Announcement to All Parties Involved or Conducting Clinical Trials in Tanzania.
    (Posted: 25th October, 2011)

  5. a) Utaratibu Mpya wa Kulipia Huduma za TFDA Kufanyika Kupitia Benki.
    (Imetolewa: 07 Oktoba, 2011)

    b) New Payment Systems for TFDA Services Through Bank Account.
    (Posted: 7th October, 2011)

  6. Tahadhari ya Uwepo wa Dawa Bandia kwenye Soko.
    (Imetolewa: 27 Septemba, 2011)

  7. Tangazo la Viwango Vipya vya Ada na Tozo 2011/2012.
    (Imetolewa: 23 Septemba, 2011)

  8. Taarifa kwa Umma Kuhusu Usalama wa Samaki Walioingizwa Nchini kutoka Japan, Tarehe 24, July 2011.
    (Imetolewa: 13 Septemba, 2011)


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