Germany · Supplements
Supplement Adverse Event Reporting in Germany
A practical guide to Supplement Adverse Event Reporting for supplements sold in Germany: who it applies to, what to prepare, and the mistakes that cause rejection.
Who needs this
- Serious adverse events must be reported to the authority within the local timeline
- Online sellers listing supplements for buyers in Germany
Documents you need
- Adverse event reporting procedure
- Ingredient and dosage review
- Product information file
- GMP certificate
Compliance checklist
Tick each item as you collect it. Saved in this browser only.
How to comply
- Set up adverse event handling
- Check whether ingredients are permitted locally
- Prepare the product information file
- Register or notify where required
Brief for your lab or agent
Copy this into an email, then edit the product and channel.
Request: Supplement Adverse Event Reporting — Germany Product category: Supplements Authority: Germany national regulator Legal basis: National supplements requirements in Germany Documents we already have: 1. Adverse event reporting procedure 2. Ingredient and dosage review 3. Product information file 4. GMP certificate Questions: 1. Does our product fall under Supplement Adverse Event Reporting in Germany? 2. Which test standards or evidence do you accept? 3. What is the current fee and lead time? 4. Is a local representative required, and can you act as one?
Cost and timeline
Before sale; notification review takes weeks.
Dossier and testing costs vary by ingredient.
Common rejection reasons
- Serious event not reported
- Ingredient not permitted
- Claims too strong for the category
- Label missing required warnings
Official sources
FAQ
Who needs Supplement Adverse Event Reporting in Germany?
Serious adverse events must be reported to the authority within the local timeline Online sellers listing supplements for buyers in Germany.
What documents are required for Supplement Adverse Event Reporting?
Adverse event reporting procedure; Ingredient and dosage review; Product information file; and gmp certificate.
What is the first step for Supplement Adverse Event Reporting?
Set up adverse event handling. Before sale; notification review takes weeks.
How long does Supplement Adverse Event Reporting take?
Before sale; notification review takes weeks.
How much does Supplement Adverse Event Reporting cost?
Dossier and testing costs vary by ingredient.
What happens if I sell without it?
Seizure, fines, and listing removal.
Who regulates Supplement Adverse Event Reporting in Germany?
Germany national regulator.
Related requirements
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