aca24@aca-pharma.de/ +49 341 223 292 36

Product notification according to the CLP Regulation – Live dossier creation in IUCLID

Individual Inhouse Online Seminar – upon request

Formulators and importers of mixtures that are classified as hazardous have to submit a mixture notification (‘Poison Centre Notification’) via ECHA’s PCN portal – regardless of the tonnage. Part of this notification is the Unique Form Identifier – the UFI code.

In our interactive online seminar, you will get to know,

  • which regulatory requirements of the product notification (Art. 45 & Annex VIII, CLP) apply to you,
  • which sources of information you can use to prepare the notification dossier and
  • how to carry out a central (EU-wide) product notification via PCN (ECHA); also for Northern Ireland & UK (‘NPIS’) in IUCLID.

We will prepare the product notification live in IUCLID using an example. You can create your own product notification in parallel and submit it via the ECHA’s PCN portal.

For further information or questions about the seminar, please contact:

Bianca Leubner
Telefon: +49 (0) 341-223 292 36
Email: aca_campus@aca-pharma.eu

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