WELCOME TO TFDA

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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ADVERSE EFFECTS
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]
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PUBLIC EDUCATION

The authority provides education to the public about food, drugs, cosmetics and medical devices. For more information   Click here  

Functions of TFDA

Tanzania Food and Drugs Authority (TFDA), is a regulatory body responsible for controlling the quality, safety and effectiveness of food, drugs, herbal drugs, cosmetics and medical devices. It is established under Tanzania Food, Drugs and Cosmetics Act No. 1 of 2003, after repealing the Pharmaceutical and Poisons Act No. 9 of 1978 (which established the Pharmacy Board) and Food {Control of Quality} Act No. 10 of 1978 (which established the National Food Control Commission). TFDA, a semi-autonomous body under the Ministry of Health and Social Welfare, became operational on 1st July 2003.

The Mission of TFDA is to protect the health of consumers against hazards associated with food, drugs, herbal drugs, cosmetics and medical devices. This mission is achieved by performing the following core activities

Product Evaluation and Registration
In Tanzania drugs, prepackaged food, cosmetics, herbal drugs, medical devices and food supplements are evaluated and registered by the Tanzania Food and Drugs Authority (TFDA)  before being approved for distribution and marketing in the country. The objective of the evaluation and registration is to ensure that only safe, quality and efficacious products are approved for use in the country. This section provides information on all aspects of the product evaluation and egistration.

Premises Registration and Licensing
The Directorate of Inspection and Surveillance is responsible with ensuring that all dealings in food, drugs, herbal drugs, cosmetics and medical devices are done after obtaining relevant licenses and permits. This section of the site gives details on the types of licenses and permits issued by TFDA and how to obtain them.

Inspection and Surveillance
 

The Directorate of Inspection and Surveillance is responsible with inspecting manufacturers, wholesalers and retailers and clinical trials sites and at port of entry to ensure that standard requirements for food, drugs, herbal drugs, cosmetics and medical devices are complied to. This section of the site describes the work of the Inspectorate.

Import and Export Control
The TFDA control import and export of food, drugs, herbal drugs, cosmetics and medical devices in order to ensure their safety, quality and effectiveness. This section of the site gives details on the procedures to be followed by importer and exporters.

Post Marketing Product Risk Analysis
TFDA continually monitor safety of food, drugs, herbal drugs, cosmetics and medical devices available on the Tanzania market. This section of the site explains how TFDA conduct Post marketing product risk analysis.


 
 
  1. 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
    (Posted: 1st Septemba, 2010 )

  2. 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.
    (Posted: 26th August, 2010 )

  3. Taarifa kwa Umma Kuhusu Kuwepo katika soko Vyakula ambavyo ni Bandia au ambavyo Havijasajiliwa
    (Posted: 13th August, 2010 )

  4. Kusitisha na kudhibiti matumizi ya sindano za kawaida (Standard Disposable Syringes) na kuimarisha matumizi ya
    Sindano zinazojiharibu baada ya matumizi (Autodisable Syringes)

    (Posted: 6th Mei, 2010 )

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

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

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

WHO IS WHO AT TFDA ?
 
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