Informationsbeauftragte für Pharmazieunternehmen mitteilen
Inhalt
Display the person responsible for information in accordance with the Medicinal Products Act
Begriffe im Kontext
nicht vorhanden
- Vorschriften für und Anforderungen an Erzeugnisse
- Erlangung von Lizenzen, Genehmigungen oder Zulassungen im Hinblick auf die Gründung und Führung eines Unternehmens
Fachlich freigegeben am
07.08.2023
Fachlich freigegeben durch
Ministry of Science and Health Rhineland-Palatinate (MWG)
If there are several information officers, you must clearly delineate their areas of responsibility. In order to assess the demarcation, you must submit the regulations that you, as the permit holder, have laid down in writing or electronically.
In Rhineland-Palatinate, you must submit the documents in the following form:
- Licence to practise medicine / certificate of study (official or notarized copy)
- Proof of practical experience (Signed original; Interim certificates: officially certified copy)
- Curriculum vitae (signed original)
- Certificate of good conduct (original, document type "OB" - sent directly to the authority)
- Form "Declaration of Designation" (signed original)
- Declaration of commitment (signed original)
Gebühr:
17€ - 293€
The fees will be charged at the end of the procedure with the notification being sent.
Mehr erfahren
If you submit your application via the online service, you must submit the required evidence to the competent authority in the original or as a certified copy.
3 - 6 Woche(n)
If the documents to be submitted are incomplete or insufficient, the processing time will be extended accordingly.
Initial application: prior to the placing on the market of finished medicinal products.
Change/change of the person responsible for information: as soon as possible, at least 6 weeks in advance