The 2017 appropriation act highlighting the various Expenditures for the ministry of environment

These guidelines are for the interest of the general public and in particular, importers of finished bulk food, food raw materials and animal feed into Nigeria. The document emphasizes that no finished bulk food and/or food raw materials should be imported without obtaining Import Permit. It also provides for payment, submission of documents for first endorsement, joint inspection of consignment, second endorsement, the release of consignment and tariff.

These guidelines are developed for the interest of the general public and in particular, importers of Narcotic and Controlled Substances, Pharmaceutical raw materials and restricted chemicals into Nigeria. The document emphasizes that pharmaceutical raw materials and restricted chemicals should not be imported without obtaining an Import permit and permit to clear where applicable.

These guidelines are for the interest of the general public and in particular importers of finished pharmaceutical, nutraceutical and herbal products (Human and Veterinary) into Nigeria. The document provides for payment, submission of documents for first endorsement, first endorsement, and joint inspection of consignment, second endorsement and release of the consignment.

These guidelines are for the interest of the general public and in particular, importers of food products into Nigeria. The document provides the procedures for application, verification of the application, payment, submission of application, review of the application, first endorsement, joint inspection of consignment, second endorsement, the release of consignment and tariff.

These guidelines are for the interest of the general public and in particular, importers of cosmetics and medical devices into Nigeria. The document emphasizes that no cosmetics and medical devices shall be manufactured, imported, exported, advertised, sold, distributed or used in Nigeria unless it has been registered under the provisions of the National Agency for Food and Drug Administration and Control (NAFDAC) Act CAP N1 (LFN) 2004, other related legislations and the accompanying guidelines.

These guidelines are for the interest of the general public and in particular importers of general chemicals, agrochemicals and raw materials into Nigeria. The document emphasizes that no general chemicals, agrochemicals or raw materials shall be imported without obtaining an Import permit or approval. It provides for payment, submission of documents for first endorsement, joint inspection of consignment, second endorsement and release of the consignment.

These guidelines are for the interest of the general public and in particular individuals and organizations intending to conduct clinical trials in Nigeria. This document emphasizes that no person shall import, procure or manufacture a drug product, cosmetic or medical device for a clinical test in Nigeria unless he is a holder of a valid clinical trial approval and the trial is to be conducted under the terms of the approval and the provisions of any regulations in force.

The guideline has an overall objective to encourage and facilitate timely paediatric medicinal product development in Nigeria. It provides an outline of critical issues in paediatric drug development and the approaches to the safe, efficient and ethical study of medicinal products in the paediatric population.

This document details the minimum requirements for accreditation to sell and supply ionizing radiation generating equipment – Diagnostic Radiology for medical applications. It emphasizes that the requirements should be applied in addition to the Nigerian Radiation Safety in Diagnostic and Interventional Radiology Regulations 2006; the Nigerian Radiation Safety in Radiotherapy Regulations 2006; and the Nigerian Radiation Safety in Nuclear Medicine Regulations 2006.

These regulations apply to cocoa and cocoa products that are manufactured, imported, exported, advertised, sold, distributed or used in Nigeria. The document provides information on labels, conditions for claims that food is cocoa-based, prohibitions, maximum limits of contaminants, permitted additives, penalty, and forfeiture after conviction.

These regulations apply to procedures and processes that will ensure appropriate importation, exportation, manufacturing, storage, warehousing, distribution, inspection, use for medical and scientific purposes, disposal as well as documentation of controlled medicines in Nigeria, in such a manner as to maintain the security and integrity of the product throughout the supply chain. They provide information on prohibition, application of registration, validity, Suspension or cancellation of certificate of registration, permit or authorization, importation of controlled medicines, labelling, storage facility, distribution, procurement, selection and quantification, inspection, dispensing disposal of controlled medicines, penalty, and forfeiture after conviction.

These regulations apply to all advertisements and promotion of cosmetics products (both single and compound entity) manufactured, imported, exported, sold, distributed or used in Nigeria.

These regulations provide for the registration of all cosmetics manufactured, imported, exported, advertised, sold, distributed or used in Nigeria. It provides information on labelling information and the net content of cosmetic products.

These regulations guide the manufacture, import, export and distribution of safe cosmetics products and penalties for offenders of the regulations.

This document provides the Nigerian Nuclear Regulatory Authority (NNRA) minimum requirements for authorization of diagnostic radiology facilities in Nigeria. It states that the requirements should be applied in addition to the Nigerian Basic Ionizing Radiation Regulations 2003; the Nigerian Radiation Safety in Diagnostic and Interventional Radiology Regulations 2006; the Nigerian Radiation Safety in Radiotherapy Regulations 2006; and the Nigerian Radiation Safety in Nuclear Medicine Regulations 2006.

This document provides the Nigerian Nuclear Regulatory Authority (NNRA) requirements for authorization of diagnostic radiology practice.

Nigerian Nuclear Regulatory Authority (NNRA) requirement for registration of drilling rig to an NNRA authorized client. It emphasizes that NNRA requires that rig owners intending to lease their rigs for storage or handling of radioactive sources to only one NNRA licensed client with valid authorization need to obtain a certificate of registration of premises for those rigs.

The 2017 appropriation act highlighting the various Expenditures for the FCSC

These regulations apply to all advertisements or promotion of drug products both single and compound entities, manufactured, imported, exported, sold, distributed or used in Nigeria. It emphasizes that no person shall advertise any drug or related product unless it has been registered by the Agency. No person shall advertise any drug product unless the advertisement has the pre-clearance and approval of the Agency; and no person shall engage in consumer promotions of any kind, including but not limited to gifts or free samples of drug or related products to the consuming public.