What is the meaning nafdac19.07.2021
7 Functions of NAFDAC in Nigeria
Dora Akunyili is head of Nigeria's National Agency for Food and Drug Administration and Control (NAFDAC). Salute to a brave fighter Some have been banned outright by NAFDAC due to research showing they contain high percentages of bleaching agents such as hydroquinone, mercury and corticosteroid. Fake body creams are epidemic in Nigeria. 20th March, – Covishield tm Vaccine Is Astrazeneca/Oxford University Vaccine; 18th February, NAFDAC Approves Covid19 Vaccine 15th January, – Safety Of Covid Vaccines: What NAFDAC Wants The Public To Know; 25th October, – NAFDAC Blacklists Mars Remedies, India For Manufacturing Falsified Medicines, Delists Pinnacle Nigeria Ciprofloxacin mg.
Suggest new definition. References in periodicals archive? Adeyeye said that NAFDAC would be strict in the regulation and control of herbal products, to facilitate its development and contribution to the national health care delivery system in Nigeria. NAFDAC first used a hologram made tje Optaglio several years earlier to authenticate and protect certificates issued to registered suppliers and manufacturers; these certificates were numbered and the registration number showed on the packaging box or label for every product on the market.
Nigeria Commits to Hologram. Nigerian government realizes the responsibility of protecting the citizens, by not only promulgating laws and decrees but also creating regulatory agencies like SON, NAFDACetcetera to ensure compliance Ofuani etal. This provides suggestive evidence that meainng has been a trend shift in drug quality how many tomatoes from one plant time in Wha, Nigeria, which may partly be ascribed to the introduction of spectrometers by NAFDAC.
The impact of improved detection technology on drug quality: a case study of Lagos, Nigeria. A growing headache: the prevalence of international counterfeit pharmaceutical trade in developing African nations.
Last week, the NAFDAC issued a press release stating those fake anti-malarial generic pharmaceuticals with the label 'Made in India' were actually found to have been produced in China. Govt to protest against 'Made-in-India' Chinese drugs. Akunyili said the NAFDAC had visited 1, drugs outlets, pharmacies, patent medicine stores, market stalls, clinics and hospitals, where bottles of "My Pikin" were recovered.
Salute to a brave fighter. Some have been banned outright by NAFDAC due to research showing they contain high percentages of bleaching agents such as hydroquinone, mercury and corticosteroid. Fake body creams are epidemic in Nigeria. Acronyms browser?
NAFDAC stands for National Agency for Food and Drug Administration and Control (Nigeria). National Agency for Food and Drug Administration and Control + 17 variants. Nigeria, Business, Product. Nigeria, Business, Product. 1. NAFDAC. National Agency for Foods Drugs Administration and Control. 1. Search for abbreviation meaning, word to abbreviate, or category. Shortcuts for power users - examples. The National Agency for Food and Drug Administration and Control (NAFDAC) is a Nigerian federal agency under the Federal Ministry of Health that is responsible for regulating and controlling the manufacture, importation, exportation, advertisement, distribution, sale and use of food, drugs, cosmetics, medical devices, chemicals and packaged water.
NAFDAC also regulates and controls quality standards for cosmetics, medical devices, detergents, vaccines, chemicals and pesticides, agrochemicals, veterinary products, herbal preparations, packaged water and related products whether imported or manufactured in Nigeria.
So, for most Nigerians, the NAFDAC stamp of approval on any food and drug item gives a sense of security and a feeling of confidence that the product is safe for consumption. Established by the NAFDAC Act, Cap N1, Laws of the Federation, , it is the lead Agency for food safety and quality and has a mission to safeguard public health by ensuring that only the right quality food, drugs and other related products are manufactured, exported, imported, advertised, sold and used.
These organizations are encouraged to self-regulate their practices and can easily arrange for consultative meetings with the Agency where their views and concerns are addressed and taken into account when making regulatory decisions that concern them.
Such an arrangement also enables NAFDAC to organize targeted and focused capacity building training programmes for the various groups. Consultative meetings could also be targeted at giving information and enlightening the public on NAFDAC requirements, discussing perceived regulatory challenges, identifying international best practices and regulatory trends, etc.
The Agency employs a structured and systematic procedure for product registration at the end of which the product is assigned a NAFDAC Registration Number — which is an attestation to the safety, quality and appropriateness for its intended use. The registration process involves:. The permit to import samples for registration purposes is issued if documentation is satisfactory.
Labeling : Labels should be informative, clear and accurate; indicate the name of product; name and address of the manufacturer, packer, distributor, importer, exporter, or vendor; make provision for NAFDAC Registration Number; batch number, manufacturing date and expiry or best before date; net content, ingredients list in metric weight in case of solids, semi-solids and aerosols and metric volume in case of liquids. Inspection : Good Manufacturing Practice GMP inspection of the production facility is carried out prior to registration of the product.
Product Approval Committee Meetings : A three 3 tier product approval meeting is held to consider the documentation, laboratory reports, GMP inspection reports and product labels prior to its registration. In recent years, the Agency seems to have become more active and stringent in enforcing existing food laws, which has increased the level of awareness of the consumer to make informed choices and has also encouraged local producers.
NAFDAC regulations require food labelling to be informative and accurate and not fraudulent or misleading. Net content, specifying essential ingredients in metric weight for solids and metric volume for liquids.
Food additives and colours must be declared on the label. Spices, flavours and colours may be listed as such, without naming the specific material, but any artificial colour or flavour should be identified as such. Labelling should be in English. If it is in another language, an English translation must be shown on the label or package insert where applicable.
With the standard U. Foreign labels must be adhered prior to the product arrival in the Nigerian port of entry. For production and expiry dates, Nigerians write the date before the month. Nutritional labelling is mandatory for any prepackaged food item for which the manufacturer makes a nutrition or dietary claim. Labels must contain directions for safe usage, cautions such as interactions when taken with other drugs. No specific waste disposal laws or product recycling regulations impact imported food products and NAFDAC does not impose any specific restrictions on packaging materials.
However, plastics must be of food grade and should not leach into the product. According to the Acting Director-General of the agency, Mrs Yetunde Oni, the guidelines provided detailed direction to assist relevant stakeholders in complying with NAFDAC regulations and spelt out details of how the agency expected regulations are to be implemented. They are to be used in conjunction with other relevant and extant statutes in the country.
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