Kudi Konsult guarantees you a comprehensive consulting service throughout the NAFDAC approval process and this involves a careful analysis of your product, advice on best practices, interface with NAFDAC and follow-up to ensure the registration is completed speedily.
To get started you can click on the Start Now button which will lead you to a self service dashboard where you can input all necessary information for the service you desire and make payment online. If you would prefer to talk to a Consultant please hit the chat button below or call 0909 505 5379 (Available Mon-Fri 9am-5pm)
FAQs ON NAFDAC REGISTRATION IN NIGERIA
In order to register a product with NAFDAC, you must first critically examine the guidelines applicable to the product and fulfill all requirements and conditions attached. Afterwards, you may check this link and click e-Registration for Registration form and Guidelines.
However, the procedure is as follows;
You prepare and submit your application form together with all supporting documents.
You make payment as assessed.
The documents are verified and a date for inspection of facility is fixed.
The inspection of the facility/ sampling of products is done, followed by laboratory analysis of the product.
Final vetting and approval meeting follow.
Then the NAFDAC Registration Number and certificate of registration is issued.
The documents include:
Evidence of Registration with Corporate Affairs Commission (CAC) (Business Name and/ or incorporation)
Site use Agreement (Where applicable)
Evidence of Trademark approval (optional for micro scale enterprise)
One vetting Sample and three labels
Copy of Receipt of Payment for production registration
Food handler’s certificate / medical fitness certificate for production staff, this should include the following: Sputum test, stool test, Urinary test, Widal test, Hepatitis B test.
SOPs for production, distribution /Recall, Quality assurance, Cleaning of equipment, receiving of packaging materials, Personal Hygiene, and for cleaning of the environment (for small-scale enterprises)
Water analysis (where applicable) List of raw material and their source(s)
Certificate of analysis of raw materials (optional for micro scale)
Certificate of analysis of finished products (optional for micro scale)
A signed and endorsed certificate of Pharmaceutical Product (for drug products)
Original copy of the Power of Attorney from the product manufacturer (if imported).
Letter of invitation from manufacturer to inspect factory abroad, full names and site of plant (where applicable)
Permit to import samples (for imported products)
Certificate of Free Sale (for imported products)