Tag: NAFDAC

  • NAFDAC seeks remedy for victimsof counterfeit antibiotic injections

    NAFDAC seeks remedy for victimsof counterfeit antibiotic injections

    The National Agency for Food and Drugs Administration and Control (NAFDAC) has called on consumers and healthcare professionals who have fallen victim to the counterfeit Meronem 1g injection currently being sold in different parts of the country to immediately seek medical advice and report to the nearest NAFDAC office.

    While alerting consumers and healthcare providers on a batch of counterfeit Meronem 1g Injection in circulation, NAFDAC urged victims to report adverse effects related to the use of the medicine to NAFDAC office or through the use of the E-reporting platforms available on its website: www.nafdac.gov.ng.

    In a public circular numbered 036/2023 and signed by the Director-General of the agency, Prof. Mojisola Adeyeye, in Abuja, she said the agency was notified about the injection by the Marketing Authorisation Holder, Pfizer, who reported the incident, as received through a patient notification platform.

    The NAFDAC boss noted that Pfizer reported that the vial content did not dissolve when reconstituted for use and that further visual inspection of the pack was observed.

    The circular also reported that the crimp code did not match the code reported on the production documentation batch of 2A21F11, which is the semi-finished batch used for 4A21I17.

    “The vial label compares favourably to the purported artwork version,” Adeyeye said, adding that the production process did not meet Pfizer’s specifications.

    “Meronem (Meropenem trihydrate injection) is an antibiotic used to treat skin and abdominal (stomach area) infections caused by bacteria and meningitis (infection of the membranes that surround the brain and spinal cord) in adults and children 3 months of age and older,” the NAFDAC boss said.

    “The administration of the counterfeit product will pose a high risk to patients as the quality and safety are not guaranteed,” she added.

    Prof. Adeyeye, however, said that healthcare providers and patients have been advised to obtain all medical products from authorised/licensed suppliers, adding that the products’ authenticity and physical condition should be carefully checked before purchase and administration.

    She also implored importers, wholesalers and retailers to maintain vigilance within the supply chain and desist from illegal importation, distribution, and sale of the counterfeit Meronem 1g injection and other substandard medicinal products.

    She further warned that anybody in possession of the counterfeit product should stop using it, adding that it should be submitted to the nearest NAFDAC office, while calling on those in possession of the counterfeit product to seek immediate medical advice from a qualified healthcare professional if they already used the product, or suffered from any adverse reaction after using the product.

    The Agency has also warned the Nigerian public against the consumption of a recalled energy drink known as ‘G Fuel’ due to the high level of caffeine it contains.

    Read Also: NAFDAC alerts Nigerians to fake injection in circulation

    The warning which came from a public alert with No. 034/2023, issued in Abuja by NAFDAC Director General, noted that the brand of energy drinks manufactured by T&E Imports and GPAE Trading Corp, was not registered by NAFDAC and has the potential of causing headaches, insomnia, irritability, and nervousness.

    Adeyeye also said the energy drink had been recalled by the Netherlands Food and Consumer Product Safety Authority (NVWA) and the Canadian Food Inspection Agency (CFIA).

    “The product is not registered by NAFDAC, which implored consumers and retailers to refrain from using, selling, serving, or distributing the implicated product,” the DG said.

    “Members of the public are encouraged to report any suspicion of distribution and sale of unwholesome packaged food products to the nearest NAFDAC office.

    “Healthcare professionals and patients are also encouraged to report adverse events or side effects related to the use of any substandard NAFDAC-regulated product to the nearest NAFDAC office.

    “NAFDAC could also be reached on 0800-162-3322 or via email: sf.alert@nafdac.gov.ng or at pharmacovigilance@nafdac.gov.ng,” she added.

    Adeyeye also cautioned pregnant women not to take the products because of the possible health effects of consuming too much caffeine which include the risk of miscarriage and a chance of low birth weight.

  • NAFDAC alerts Nigerians to fake injection in circulation

    NAFDAC alerts Nigerians to fake injection in circulation

    The National Agency for Food and Drug Administration and Control (NAFDAC) has alerted Nigerians, particularly healthcare providers, to one batch of counterfeit Meronem 1g injection in circulation across the country.

    The information is contained in a public alert Number 036/2023 by the agency’s Director General, Prof. Mojisola Adeyeye, and issued to the News Agency of Nigeria (NAN) yesterday in Abuja.

    Adeyeye said the Marketing Authorisation Holder (MAH), Pfizer, reported the incident, as received through a patient notification platform on a suspicious park of Meronem 1g injection purchase.

    She quoted Pfizer as saying the vial content did not dissolve when reconstituted for use and that further visual inspection of the pack was observed.

    It was also reported that the crimp code did not match the code reported on the production documentation batch of 2A21F11, which is the semi-finished batch used for 4A21I17.

    Adeyeye said the production process did not meet with the Pfizer’s specifications.

    “The vial label compares favourably to the purported artwork version.

    “Meronem (Meropenem trihydrate injection) is an antibiotic used to treat skin and abdominal (stomach area) infections caused by bacteria and meningitis (infection of the membranes that surround the brain and spinal cord) in adults and children from three months old and older.

    “The administration of the counterfeit product will pose a high risk to patients as the quality and safety are not guaranteed,” she said.

    The NAFDAC boss said healthcare providers and patients were advised to obtain all medical products from authorised/licensed suppliers.

    She advised that products’ authenticity and physical condition should be carefully checked before purchase and administration.

    Adeyeye also implored importers, wholesalers and retailers to maintain vigilance within the supply chain and desist from illegal importation, distribution, and sale of the counterfeit Meronem 1g injection and other substandard medicinal products.

    Read Also: NAFDAC gets Global Fund’s $933m grant

    The NAFDAC boss said anybody in the possession of the counterfeit product should stop using it and submit it to the nearest NAFDAC office.

    She also urged those with the possession of the counterfeit product to seek immediate medical advice from a qualified healthcare professional, if they have used the product, or suffered from any adverse reaction after using the product.

    Adeyeye also advised healthcare professionals and consumers to report any suspicion of adverse drug reactions, or substandard and falsified medicines to the nearest NAFDAC office, or NAFDAC phone number on 0800-162-3322 or via email: sf.alert@nafdac.gov.ng.

    The NAFDAC also urged healthcare professionals and patients to report adverse events or side effects related to the use of a medicinal product to the nearest NAFDAC office, or through the use of the E-reporting platforms available on the NAFDAC website www.nafdac.gov.ng.

    She advised members of the public to report any adverse effect of the product via the Med- safety application available for download on android and IOS stores or via e-mail on pharmacovigilance@nafdac.gov.ng.

  • NAFDAC alerts Nigerians to counterfeit injection in circulation

    NAFDAC alerts Nigerians to counterfeit injection in circulation

    The National Agency for Food and Drug Administration and Control (NAFDAC) has alerted Nigerians, particularly healthcare providers, to one batch of counterfeit Meronem 1g Injection being purchased in Nigeria.

    The information is contained in a public alert No. 036/2023, signed by the Director-General of the agency, Prof. Mojisola Adeyeye, and issued to the News Agency of Nigeria (NAN) in Abuja on Tuesday.

    Adeyeye said the Marketing Authorization Holder (MAH) Pfizer, reported the incident, as received through a patient notification platform, concerning a suspicious park of Meronem 1g injection purchase.

    She reported Pfizer as saying that the vial content did not dissolve when reconstituted for use and that further visual inspection of the pack was  observed.

    It was also reported that the crimp code did not match the code reported on the production documentation batch of 2A21F11, which is the semi-finished batch used for 4A21I17.

    Read Also: LASU VC cleared over alleged certificate racketeering

    The D-G said that the production process did not meet with the Pfizer’s specifications.

    “The vial label compares favourably to the purported artwork version.

    “Meronem (Meropenem trihydrate injection) is an antibiotic used to treat skin and abdominal (stomach area) infections caused by bacteria and meningitis (infection of the membranes that surround the brain and spinal cord) in adults and children 3 months of age and older.

    “The administration of the counterfeit product will pose a high risk to patients as the quality and safety are not guaranteed,” Adeyeye said.

    The NAFDAC boss, however, said that healthcare providers and patients were advised to obtain all medical products from authorised/licensed suppliers.

    According to her, products’ authenticity and physical condition should be carefully checked before purchase and administration.

    She also implored importers, wholesalers and retailers to maintain vigilance within the supply chain and desist from illegal importation, distribution, and sale of the counterfeit Meronem 1g injection and other substandard medicinal products.

    Adeyeye said that anybody in the  possession of the counterfeit product should stop using it, as well as submit it to the nearest NAFDAC office.

    She also called on those with the possession of the counterfeit product to seek immediate medical advice from a qualified healthcare professional if they already used the product, or suffered from any adverse reaction after using the product.

    The D-G also advised healthcare professionals and consumers to report any suspicion of adverse drug reactions, or substandard and falsified medicines to the nearest NAFDAC office, or NAFDAC phone number on  0800-162-3322 or via email: sf.alert@nafdac.gov.ng.

    Adeyeye also encouraged healthcare professionals and patients to report adverse events or side effects related to the use of a medicinal product to the nearest NAFDAC office, or through the use of the E-reporting platforms available on the NAFDAC website www.nafdac.gov.ng.

    The public are also urged to report any adverse effect of the product via the Med- safety application available for download on android and IOS stores or via e-mail on pharmacovigilance@nafdac.gov.ng

    (NAN) (www.nannews.ng)

  • NAFDAC gets Global Fund’s $933m grant

    NAFDAC gets Global Fund’s $933m grant

    The National Agency for Food and Drug Administration and Control (NAFDAC) has got the green light to access Global Fund’s 2024-2026 grant of $933 million to Nigeria, The Nation learnt yesterday.

    The Global Fund is an international financing institution dedicated to combating HIV/AIDS, Tuberculosis, as well as Malaria and Resilient and Sustainable Systems through support to countries in their efforts to address global health challenges and strengthen health systems.

    The National Agency for the Control of AIDS (NACA) is the principal recipient of the fund.

    NAFDAC’s Director General, Prof. Mojisola Adeyeye, announced that the management of the agency’s $2 million component of the outgoing Global Fund 2021-2023 grant was responsible for its further inclusion as a beneficiary of the fund’s 2024-26 grant.

    Adeyeye, who spoke at a meeting with the Global Fund and the National Agency for the Control of AIDS (NACA) in Abuja, said through vital support from the Global Fund’s Resilient and Sustainable Systems for Health (GF-RSSH) grant, NAFDAC had been met critical parts of its mandate in safeguarding the nation’s health.

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    Global Fund and NACA declared NAFDAC’s utilisation of the existing grant satisfactory.

    The acting Executive Secretary of the Country Coordinating Mechanism for Global Fund Nigeria, Mr. Ibrahim Olaitan, said the decision to continue the collaboration was due to NAFDAC’s proven transparency and accountability with the outgoing grant.

    He said NAFDAC’s management of the grant met all criteria to guarantee its participation in the next grant, adding: “The NAFDAC support is cross-cutting for laboratory strengthening, quality control, and quality assurance for the ATM products.”

    Corroborating Global Fund, NACA’s Director General Gambo Aliyu said: “With $2 million, this is remarkable and this is what we want to encourage to see more for the entities we disbursed money to. We want to hold this kind of a meeting to hear from them to tell us what they do. In terms of transparency, Global Fund’s money is very safe with NAFDAC.”

  • NAFDAC to benefit from Global Funds $.9b grant to Nigeria

    NAFDAC to benefit from Global Funds $.9b grant to Nigeria

    The National Agency for Food and Drug Administration and Control (NAFDAC) has received approval to benefit from the Global Fund’s grant of $933 million for Nigeria covering the period 2024-2026, according to a statement on Monday, November 6.

    The Global Fund is an international financing institution dedicated to combating HIV/AIDS, Tuberculosis, and Malaria and Resilient and Sustainable Systems through support to countries in their efforts to address global health challenges and strengthen health systems.

    The National Agency for the Control of AIDS (NACA) is the principal recipient of the fund.

    According to the Director General (DG) of NAFDAC, Prof Mojisola Adeyeye, the management of the NAFDAC’s $2m component of the outgoing Global Fund 2021-2023 grant was responsible for the agency’s further inclusion as a beneficiary from the Fund’s 2024-26 grant.

    Adeyeye, at a meeting with the Global Fund and the National Agency for the Control of AIDS (NACA) in Abuja, said through vital support from the Global Fund’s Resilient and Sustainable Systems for Health (GF-RSSH) grant, NAFDAC has been able to meet critical parts of its mandate in safeguarding the nation’s health space.

    Global Fund and the National Agency for the Control of AIDS (NACA) declared NAFDAC’s utilization of the existing grant satisfactory.

    Ibrahim Olaitan, the acting Executive Secretary, Country Coordinating Mechanism for Global Fund Nigeria said the decision to continue with the collaborations was down to NAFDAC’s proven transparency and accountability with the outgoing grant.

    He said NAFDAC’s management of the grant met all criteria to guarantee its participation in the next grant, adding, “The NAFDAC support is cross-cutting for laboratory strengthening, quality control and quality assurance for the ATM products”.

    Corroborating Global Fund, NACA’s DG, Gambo Aliyu said: “With $2m, this is remarkable and this is what we want to encourage to see more for the entities we disbursed money to. We want to hold this kind of meeting to hear from them to tell us what they do. In terms of transparency, Global Fund money is very safe with NAFDAC”.

    Among other areas the $2.3m 2021-23 grant was able to strengthen, Adeyeye said: “Under the GF-RSSH grant, several budget lines were implemented by NAFDAC during Grant Cycle 6, totalling $2,305,695.03, for strengthening NAFDAC role and capacity in pharmacovigilance and ADR monitoring and reporting-$36,965.00.

    Read Also: NAFDAC to review sanction on exporters of substandard products

    “$944,605.00 for strengthening one of the NAFDAC ISO 17025 laboratories (CDCL Yaba) to conduct a comprehensive analysis of ATM and other disease program medicines.

    “The purpose is to support and strengthen existing NAFDAC Laboratories to sustain their ISO-17025 Accreditation and to get WHO Prequalification.

    “It is good to share the success story that the Central Drug Control Laboratory, Yaba has attained World Health Organisation Prequalification, partly because of the GF support.

    “Another impactful support from GF was the support to NAFDAC for phased implementation of traceability of health products at $1,131,328.82 – BL136.

    “This budget line has been instrumental in rolling out a phased implementation of traceability for health products in Nigeria.”

  • NAFDAC to review sanction on exporters of substandard products

    NAFDAC to review sanction on exporters of substandard products

    The National Agency for Food and Drug Administration and Control (NAFDAC) has promised to review sanctions for exporters of substandard products.

       The Director-General of NAFDAC, Prof Mojisola Adeyeye, said this at a news conference, while expressing displeasure at the level substandard goods were being rejected in some foreign countries.

    She said the agency has been able to identify some of the reasons, including non-compliance to guidelines established by NAFDAC to encourage participatory exports.

    Adeyeye stated that almost all exported food products were being processed in the country without the statutory testing by NAFDAC. According to her, some of the goods are exported without NAFDAC’s quality control and safety tests hence their rejection.

    Other reasons included the non-utilisation of hitherto free laboratory testing by NAFDAC for export samples, coupled with the connivance of unscrupulous agents. Also identified was the exclusion of NAFDAC’s requirements for its regulated products in the mandatory pre-shipment inspection in the National Export Supervision Scheme (NESS) as administered by the Federal Government appointed Pre-shipment Inspection Agents (PIAs).

    Adeyeye stated that some of the exporters were unwilling to comply with minimal sanitary and phytosanitary measures required for exports to countries with stringent market access, as well as poor packaging by some manufacturers.

    The NAFDAC boss noted that many exporters have formed the habit of disregarding importation requirements of trading partner countries. She also mentioned “penchant for sourcing from open markets for exports without any form of minimal safety or quality specifications and unwillingness to invest in pre-export activities that help to ensure sustainable export”.

    Read Also: NAFDAC destroys N5.4m of unwholesome drugs, food

    The DG boss said to ratify these challenges as part of the outcome of its recent meeting with the United Kingdom Food Standard Agency (FSA), the agency would be commencing six regulatory measures to address the situation. She listed immediate inclusion and implementation, as a matter of urgency, NAFDAC Good Manufacturing Practices (GMP), Good Hygienic Practices (GHP) and laboratory testings such as mycotoxin, pesticide residue, and heavy metals certification for regulated food and drug products.

    She said the National Export Supervision Scheme (NESS) would also be carried out on some of these products as administered by the Federal Government appointed Pre-shipment Inspection Agents (PIAs). Other measures, she mentioned, were the inclusion of NAFDAC in the Central Bank of Nigeria (CBN) Export Proceed (NXP) form processing and engagement with the Comptroller-General of Customs as the new administrator of the Nigeria Single Window Trade portal to facilitate this.

    She said NAFDAC had earlier engaged with CBN (Trade and Exchange Division) and the Federal Ministry of Finance (Home Finance) on this same matter. She said the agency would also be strengthening in-country regulatory infrastructure on export with the introduction of NAFDAC Regulations on Export 2022. Adeyeye added that the regulation was already hosted on NAFDAC’s website with e-copy sent to exporters, trade associations and professional bodies for their input and comments within the next 60 days, which began on October 11. She said the agency would also be collaborating with the Nigerian Exports Promotion Council (NEPC) on regulation of goods.

     According to her, the agency will continue with awareness meetings with the export trade operators on the NAFDAC’s guidelines.

  • NAFDAC destroys N.5b unwholesome drugs, food

    NAFDAC destroys N.5b unwholesome drugs, food

    The National Agency for Food and Drug Administration and Control (NAFDAC) has reiterated its determination to sanitize the food and drug subsectors as it carried out the destruction of confiscated unwholesome products worth N.5b in Abuja on Wednesday.

    The destruction of the unwholesome products carried out at the Kuje dump site hollowing seizures and voluntary handover from the Federal Capital Territory (FCT) and Nasarawa State includes psychoactive and controlled substances, antibiotics, antihypertensives, antimalarials, herbal snuff, and herbal remedies either handed over, confiscated from hawkers, expired, fake, or substandard.

    The Director General (DG), Prof Mojisola Adeyeye put the estimated street value of the destroyed products at N535m.

    Reiterating NAFDAC’s determination not to relent in its efforts to sanitize the food and drugs subsector, the DG, who was represented at the destruction site by the agency’s Director, Investigation and Enforcement, Francis Ononiwu, said, “I have said it on several platforms that Drug counterfeiting is an act of economic sabotage, and it also represents a serious threat to public health, and NAFDAC under my watch has been repositioned to fight this menace.

    “The Agency has adopted a proactive approach by engaging political, traditional, faith leaders, journalists, and other Nigerians to sensitize their wards on the dangers of dealing with substandard and falsified medicines”.

    She urged Nigerians to be on the lookout for spurious and counterfeit medicines, unwholesome foods, and other regulated products and report the same to NAFDAC.

    Read Also: NAFDAC moves to harness Southeast’s potential for improved productivity

    “NAFDAC on its part will ensure continuous surveillance and heightened raids on these products and we shall continue to enforce the regulations governing these products in Nigeria”, she added.

    According to her, some of the drugs destroyed are drugs seized from criminal drug hawkers “In July this year the Agency launched a media sensitization campaign on the ‘Dangers of Drug Hawking and Ripening of Fruits with Carbide’.

    “The campaign was launched here in FCT and later taken to all the six geopolitical zones of the federation where our message highlighted the dangers of drug hawking and ripening of fruits with carbide.

    “The campaign was followed by coordinated raids on drug hawkers and also on illegal distributors of unregistered herbal medicines. These activities resulted in mop-up of expired, substandard, and falsified orthodox and traditional medicines from circulation”‘ she added.

    Some of the destroyed unwholesome products were confiscated from drug hawkers, food products such as spaghetti, vegetable oil, and non-alcoholic beverages, including a 1 X 40ft container of unregistered Faurecia instant powdered milk that was handed over to the NAFDAC by the Nigeria Customs Service (NCS).

    Also burnt were cosmetics such as creams, lotion, and pomade, including skin-lightening creams seized from spas and beauty centers; chemicals such as fake insecticides and Medical Devices; as well as expired and unwholesome products voluntarily handed over for destruction by compliant companies, Non-governmental organizations (NGOs) and Association of Community Pharmacy of Nigeria (ACPN), among others.

  • Why EU, UK, others reject Nigerian food, drug exports, by NAFDAC

    Why EU, UK, others reject Nigerian food, drug exports, by NAFDAC

    The National Agency for Food and Drug Administration and Control (NAFDAC) has declared that it will no longer tolerate the unquantifiable embarrassment brought on Nigeria by the unscrupulous exporters that sidestepped the regulator only to have their goods rejected by the country of destination.

    The agency said henceforth, no exporters should export any NAFDAC Regulated product without it being certified of its safety and quality status including full compliance with the destination country government requirements.

    According to the agency’s Director General (DG), Prof. Mojisola Adeyeye, this is to avert colossal economic loss resulting from the rejection of non-compliant exports by the trading partners and the embarrassment brought on the image of the country.

    Adeyeye, while addressing the media in Abuja on Tuesday on Nigeria’s export rejects and continued efforts of her agency to change the narrative steps have commenced on the urgent need to nip the negative trend in the bud

    She listed the reasons behind the rejection of the exported food and drug to the United Kingdom (UK), the European Union (EU), and other places, saying, “The challenge bedeviling the export process of NAFDAC regulated products especially, assuring safety and quality status of food exports in Nigeria has been traced to:/ non-compliance with advisory guidelines established by NAFDAC to encourage participatory exports.

    Read Also: NAFDAC moves to harness Southeast’s potential for improved productivity

    “Almost all exported food products are processed without the statutory testing by NAFDAC. Therefore, it is not surprising that all the items exported without NAFDAC quality control and safety tests are rejected.

    “Non-utilization of hitherto free laboratory testing by NAFDAC for export samples coupled with the connivance of unscrupulous agents.

    “Exclusion of NAFDAC’s requirements for its regulated products in the mandatory pre-shipment inspection in the National Export Supervision Scheme (NESS) as administered by the FGN appointed Pre-shipment Inspection Agents (PIAs).

    “Unwillingness of exporters to comply with minimal sanitary and phytosanitary measures required for exports to countries with stringent market access.

    “Poor packaging, disregard for importation requirements of trading partners countries f. Penchant for sourcing from open markets for exports without any form of minimal safety or quality specifications

    “Unwillingness to invest in pre-export activities that help to ensure sustainable exports as well as disinformation on the roles of NAFDAC in the pre-shipment inspection and verification exercise of container stuffing”.

    The DG however said the agency has initiated several steps to curb the negative trend while urging exporters of NAFDAC’s regulated products to take advantage of the regulations and save the country further embarrassment from the international community.

    She also disclosed that the agency is on the verge of reviewing its extant tariff-based sanction regime for recalcitrant exporters for optimal effect.

  • NAFDAC moves to harness Southeast’s potential for improved productivity

    NAFDAC moves to harness Southeast’s potential for improved productivity

    The National Agency for Food and Drugs Administration and Control (NAFDAC) has said that it has begun moves to harness the potential in the Southeast geopolitical zone for improved manufacturing productivity.

     The agency also revealed plans to work with governors of the Southeast to set up industrial hubs to revitalize the region’s economy.

     The new Zonal Director of NAFDAC in the Southeast, Martins Iluyomade, who made this known during a media parley in Enugu, noted that the Southeast is the economic heartbeat of the nation, adding that in terms of production output, the Southeast is supposed to be the China of Nigeria if well harnessed.

     “The people of the Southeast are very industrious, very innovative, very hard-working and business-minded people. My mission here is to harness all these potentials. To make sure that we are able to produce what cannot only be used locally by getting NAFDAC approvals but things for export”, Iluyomade said.

     He disclosed that the agency was willing to tap into the renewed synergy among the governors in the region for the repositioning of the zone’s economy.

     “The Southeast governors some days ago were saying that it is time to build the Southeast and build economic zones. I key into that vision seriously because I believe that the Southeast can actually be the China of Nigeria. If we are going to be self-reliant, we need people in the Southeast to rise up to their potential.

     “I see that the Southeast governors are forming a bloc. Before, they were operating in silos. But with the way things are now, I can see that they are forming a bloc. They are having several meetings to ensure that there is peace in the region and to see that they generate economic activities.

     “We have specific programmes to do with them to see how we can partner to create those industrial hubs. I am telling you that if we are able to actualise these hubs, China will come and learn from us.

     “We will send them our proposals. They are the ones driving; our duty is regulatory. Ours is that we are ready to assist them in setting up those projects, in setting up the factories and we will do all the things we are supposed to do.

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     “NAFDAC is coming on board to make sure that we fulfil the potentials of the Southeast. The nation will be better for it. We want to work with every stakeholder in this region to make this goal work.

     “And I am telling you that with certain things that have happened recently, a lot of companies are planning to relocate to the region and we will be helping them to set up”.

     The NAFDAC chief continued: “We want to create an economic hub for this country in line with the federal government agenda. There is a problem in the country which is a shortage of foreign direct investment, money not coming in from oil, so people start to look elsewhere outside oil in terms of export so we could get balance of trade.

     “If you look at which zone can do that kind of thing, it is the Southeast zone. I will engage stakeholders to achieve this. NAFDAC has come to help people attain their potential. My duty is to engage all the stakeholders to make sure that things are done in line with international best practices and NAFDAC will be there to assist.

     “We don’t want to be seen as enemies. Why NAFDAC was established was to help you to produce products that everybody can use. I am saying this now, for those who have the brain to produce imitation, the same brain can do original. One of my jobs here is to assist those doing imitation to transit to doing original. We are here to help our people build a major economic hub”.

  • NAFDAC sensitises Ibadan stakeholders on online products registration

    NAFDAC sensitises Ibadan stakeholders on online products registration

    The National Agency for Food and Drug Administration and Control (NAFDAC) has sensitised producers and marketers of its new online products and company registrations. The Oyo State Coordinator, NAFDAC, Matthew Adeoye, said during a stakeholders’ meeting in Ibadan that NAFDAC Automated Products Administration and Monitoring System (NAPAMS) offered significant reduction on the timeline for registration.

     Adeoye said that the online registration was part of the Agency’s efforts to facilitate faster processes and remove bottlenecks associated with traveling for follow-ups. “NAPAMS provides a medium for the application for products registration with NAFDAC and data capture of all existing and current products it has approved. It also offers stage-by-stage status feedback to applicants regarding update on the application. The process is seamless that an applicant can monitor (online) all the processes from registration, payment, status/stages of registered product at the applicant’s zone due to decentralisation,” he said.

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     Also, Mrs Roseline Ajayi, Director, NAFDAC South West Zonal Office, Ibadan, said the meeting sought to interact and update the stakeholders on the direction of the agency and to clarify issues with navigating the portal. Ajayi said that product quality, safety and wholesomeness must not be neglected due to the country’s current economic crises