To all Market Authorization Holders, Importers and Local Manufactures of Medicines, Medical Device, Borderline Products, and Cosmetics.
Hereby inform you all that the custom clearance of all Medicines, Medical Devices, Borderline Products, Cosmetics and Raw Materials for manufacturing will be facilitated through ASYCUDA system after 19.09.2024.
On 19.09.2024 onwards all consignees need to upload their documents to the ASYCUDA system according to the following format,
* Mandatory documents
NM4 - This becomes mandatory when requested by NMRA or product is unregistered.
NM5 - This becomes mandatory in sample importations.
CEO / NMRA