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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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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.
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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  

Control of Cosmetics Regulations

The draft cosmetics regulations which have been prepared under section 122(e) of the Tanzania, Food, Drugs and Cosmetics Act of 2003 once approved by the Minister responsible for health matters will pave a way for registration of cosmetics among other control measures.

In preparing the regulations three important principles of regulating quality and safety of cosmetics worlwide were considered:-

  1. Safety aspects of cosmetics
  2. The rights of consumers to make an informed decision based on provision of true and adequate information
  3. Enforcement aspect to enable proper regulation of cosmetics

The regulations are divided into eight parts and covers issues such as restrictions on manufacturing and sell of cosmetics, labelling instructions, registration of cosmetics, importation of cosmetics, registation of premises and licensing and promotion control

TFDA anticipates that implementation of the regulations will bring the following benefits:-

  1. Availability of safe products and of acceptable quality and hence promotion of public health
  2. Optimization of partnership with the industry
  3. Provision of necessary information to enable one make an informed choice
  4. Limit the prospect of counterfeit and poor quality cosmetics.

Click here to download the draft regulations

Previous page   Next page - (Cosmetics Products)

 
  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 )

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