The most essential and unavoidable issue is to obtain marketing authorization (MA) from the local authorities :
> Follow-up of the files
AGMED’s requirements have increased significantly as far as strict regulation is concerned and this requires special attention and rigour.
For fast, reliable and profitable file submissions, we have a team which is dedicated to the service of registering your products for submission and the monitoring and follow-up of files with the administration at the Ministry of Health.
Hence you will benefit not only from the expertise of our team, but also from privileged contacts with :
> Management of pharmacy and medicines
> National Laboratory for the control of medicines
THEY HAVE BEEN WITH US FOR 15 YEARS
Our experience is your guarantee to success