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Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has bee to make a type specimen book. It has survived not only five ged. It was in the 1960s with the release of Letraset sheets containing Lorem Ipsum passages, and more recently with desktop publishing software like Aldus PageMaker including versions of Lorem Ipsum.
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Alison Burgas
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Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has bee to make a type specimen book. It has survived not only five ged. It was popularised in the 1960s with the release of Letraset sheets containing Lorem Ipsum passages, and more recently with desktop publishing software like Aldus PageMaker including versions of Lorem Ipsum.
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PROCEDURES FOR REGISTERING NUTRACEUTICAL PRODUCT OR FOOD SUPPLEMENT BY TANZANIA BUREAU OF STANDARD (TBS) IN TANZANIA

PROCEDURES FOR REGISTERING NUTRACEUTICAL PRODUCT OR FOOD SUPPLEMENT BY TANZANIA BUREAU OF STANDARD (TBS) IN TANZANIA

TBS: Is the Tanzania Bureau of Standards established by section 3 of the Act (standard Act,          CAP.130) NUTRACEUTICAL PRODCT: According to FDA this falls in the group of Food Supplement (Dietary Supplement) since they are not intended to treat, diagnose, prevent or cure diseases. Otherwise, will be categorized as medicine and should be regulated as a Drug and should…

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MARKET AUTHORIZATION OF VETERINARY MEDICINES UNDER NATIONAL PROCEDURE IN TANZANIA AND MUTUAL RECOGNITION PROCEDURE (MRP) IN EAST AFRICA COMMUNITIES (EAC)

MARKET AUTHORIZATION OF VETERINARY MEDICINES UNDER NATIONAL PROCEDURE IN TANZANIA AND MUTUAL RECOGNITION PROCEDURE (MRP) IN EAST AFRICA COMMUNITIES (EAC)

MRP: Is application procedure for an applicant wishes to have MA granted in more than one partner state simultaneously. MARKET AUTHORIZATION (MA): An official approval of the medical product to be marketed or distributed in a respective country. MARKET AUTHORIZATION HOLDER (MAH): In other name called “APPLICANT” simply means a person or Company who/which submits an application for registration of…

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WHY PARTICIPATE? Obtaining prequalification of an in vitro diagnostic (IVD) may demand considerable investment, in terms of both financial investment and staff time (to improve production quality and/or to prepare a dossier for submission and deal with any requests for further information from WHO). But benefits may accrue to a manufacturer during and following product prequalification.  I.      Increased technical capacity…

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