Submission of manual applications for foreign manufacturing site registrations (Previous online approvals)

Please be advised that, for all foreign manufacturing site registrations previously approved via the online system, a manual dossier should be submitted.

Following supporting document submission is mandatory with the manual dossier.

• Copy of the e-NMRA manufacturing site approval certificate issued by the National Medicines Regulatory Authority
• Previous payment receipt
• Copy of the previously issued approval letter for the manufacturing site (if available)

Deadline for the submission-05/09/2026

CEO/NMRA

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