Pharmaceutical manufacturing; notification of subsequent changes and change of qualified person.
Changes with regard to a manufacturing authorization according to Section 13 of the German Medicines Act are subject to notification.
Depending on the nature of the notified change, the authorization according to Section 13 AMG may have to be changed by the drug supervisory authority.
Notification shall be made informally to the appropriate government.
The notification must be made before the intended change.
The statutory processing period is three months at the longest. The period begins to run when all documents and information are complete.
Depending on the facts reported, the documents to be submitted may differ considerably.
Please check with the appropriate authority for the required documentation.
Please select a location in "Localization" so that the address of the responsible authority can be filled in.
Prefillable Form, Bavaria-wide:
Formloser Antrag (mit Unterschrift)
This form has to be signed and sent to the responsible authority. You can sign the form manually and send it by email/fax or sign the form electronically with your qualified electronic signature an send it by (secure) email. If the responsible authority has set up a De-Mail account, you can also send the form by De-Mail using an sender-confirmed message.
On the basis of the administrative expenses incurred and the time required and the importance of the matter for the applicant, a fee of between €500 and €50,000 is set (according to the Schedule of Costs - Tariff No. 7.IX.8/Tariff item 1.1).
Responsible for editing:Bayerisches Staatsministerium für Gesundheit, Pflege und Prävention
- Online transactions, Bavaria-wide
- Online transactions, locally limited
- Form, Bavaria-wide
- Form, locally limited
- Prefillable Form, Bavaria-wide
- Legal bases, Bavaria-wide
- Legal bases, locally limited
- Fees, Bavaria-wide
- Fees, locally limited