Medicinal products for human use, manufacture
Description
The production of medicinal products for human use in Hesse is centrally monitored by the Hessian State Office for Health and Care (HLfGP). The legal basis is in particular the German Medicines Act (AMG). The Regional Council also issues permits for production as well as certificates for the import and export of pharmaceuticals.
Competent office
Hessian State Office for Health and Care (HLfGP)
Contact point
Please contact the Hessian State Office for Health and Care (HLfGP).
;Please contact the Hessian State Office for Health and Care (HLfGP).
Contact person
Hessisches Landesamt für Gesundheit und Pflege - Abteilung V Pharmazie
Address
postal address
(Zentrale Postanschrift)
Post office box 11 03 52
64218 Darmstadt
address
Contact
Internet
Required documents
Depending on the type of application (further information can be found on the homepage of the Hessian State Office for Health and Care).
Notes (specifics)
The higher federal authorities are responsible for questions regarding the approval of medicinal products, Federal Institute for Drugs and Medical Devices (BfArM), Paul-Ehrlich-Institut (PEI)
Area of validity
Hesse
Official approval
Officially approved by Hessian Ministry of Social Affairs and Integration on 25.10.2016
Keywords
Import, Arznei, Arzneimittel Herstellung, Medikamente, Pharmazie, Arzneimittel, Einfuhr, free-sales-zertifikat, Zertifikat, Handel, Export