NAFDAC

 These regulations prescribe the minimum food safety requirements for preparation, processing, manufacturing, packaging, storing, transportation, distribution, handling and offering of food for sale or supply to the consumer.

These regulations prescribe the minimum current good manufacturing practice requirements for methods to be used in, and the facilities and controls to be used for, the manufacture, processing, packing, or holding of a medicinal product for human or animal use, to ensure that such medicinal product meets the requirements of safety, and has the identity and strength and meets the quality and purity characteristics that it purports or is represented to possess.

 These regulations prescribe the minimum requirements for good distribution practice in the public and private sectors for finished pharmaceutical products and shall apply to all persons and companies involved in any aspect of the distribution of pharmaceutical products from the manufacturing site to the point of use. These include but are not limited to governments at all levels, public and private health and storage facilities, manufacturers of finished pharmaceutical products, importers, exporters, distributors, wholesalers, suppliers, retailers, freighters, forwarding agents and transporters.

These regulations prescribe the minimum current good manufacturing practice
requirements for manufacturing, processing, packaging or holding of a food or food
product for human and animal use, to ensure that such food or food products meet the requirements of safety, quality, wholesomeness and suitability for consumption.

These regulations shall apply to authorised medicinal products for human and
veterinary use and any pharmacovigilance activity connected therewith. These
regulations shall apply to but are not limited to pharmaceuticals, nutriceuticals,
traditional and complementary medicines, vaccines, biologicals and medica

These regulations prescribe good clinical practice requirements for the conduct of
clinical trials, including multi-centre trials, on participants involving medicinal products to ensure that the rights, safety and well-being of trial participants are
protected and that the results of the clinical trials are credible.

Wine Regulations 2005

Spirit Drinks Regulations 2005

Soft Drinks Regulations 2005

Processed Food Registration Regulations 2005