Notification of unexpected or adverse effects

If you become aware of information concerning your authorised biocidal product or the active substances in it, and this information may affect the authorisation, you need to notify the competent authority that granted the authorisation.

If the product has received a Union authorisation, you need to notify the European Commission and ECHA.

The notification must be submitted without delay. Refer to ECHA's Biocidal Products Regulation (BPR) pages and to the legislation, especially Article 47 of the BPR, for information on the notification of unexpected or adverse effects.

Preparing a notification

  • If you need support to prepare your notification, please contact the ECHA Helpdesk for further information.

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