![]() ![]() ![]() Once all the requirements are met, the applicant will be issued a renewed Certificate of Registration.For products approved at the meeting, ‘Notification of Registration’ is issued to the applicant while ‘Compliance Directive’ is issued to those not approved.For products labels with compliance issues, compliant artworks may be submitted with a commitment letter from manufacturer. After documentation review, required GMP inspection and Product analysis in lab, products are sent for approval meetings.Visit the NAFDAC office and submit the application package to the Liaison Office of the Director (LOD). ![]() Make sure that you have all the documents listed in the “Required Documents” section of this page.The applicant must prepare an application letter on the company letterhead addressed to the Director General requesting to get the concerned product registered.Before visiting the office, the applicant needs to perform some pre-processes which are explained in further steps.The contact link of NAFDAC can be found below contact link.To Renew License to Manufacture of Drugs for Sale in person, the applicant has to visit the office of Director General of National Agency for Food and Drug Administration and Control.
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