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Review Date: 12/12/2026 Effective Date: 13/12/2021Doc. Ref. No: R&RGDL00801National Agency for Food & Drug Administration & Control (NAFDAC)Drug Registration and Regulatory Affairs (R&R) DirectorateGUIDELINES
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Read the NAFDAC guidelines carefully to understand the requirements.
02
Gather all the necessary documentation and information needed to fill out the guidelines.
03
Fill in all the required fields accurately and completely.
04
Review the filled out guidelines to ensure all information is correct.
05
Submit the completed guidelines to NAFDAC for approval.
Who needs nafdac guidelines on good?
01
Pharmaceutical companies
02
Food and beverage producers
03
Cosmetics manufacturers
04
Medical device manufacturers
05
Importers and exporters of regulated products
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What is nafdac guidelines on good?
NAFDAC guidelines on good refer to the set of rules and regulations set by the National Agency for Food and Drug Administration and Control to ensure the quality of goods produced, distributed, or sold in Nigeria.
Who is required to file nafdac guidelines on good?
All companies and individuals involved in the manufacturing, distribution, or sale of goods in Nigeria are required to file NAFDAC guidelines on good.
How to fill out nafdac guidelines on good?
NAFDAC guidelines on good can be filled out online through the NAFDAC website or by submitting physical copies to the nearest NAFDAC office.
What is the purpose of nafdac guidelines on good?
The purpose of NAFDAC guidelines on good is to ensure that goods produced, distributed, or sold in Nigeria meet the required quality standards and do not pose any health risks to consumers.
What information must be reported on nafdac guidelines on good?
Information such as the name of the manufacturer, ingredients used, production process, storage conditions, expiry date, and batch number must be reported on NAFDAC guidelines on good.
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