Elements Advisory
Regulatory support for active substances and biocidal products

Webinar PT11/12

Webinar PT11 and PT12, biocidal product authorization

 

Webinar: Regulatory Challenges and Opportunities for PT11 and PT12 Biocidal Products

Friday, June 19, at 11:00 -12:15 am (CET)

Many active substances used in PT11 and PT12 are currently still part of the EU Review Programme and the end of their evaluation is approaching.

⚠️Active substance approvals can be expected relatively soon; prepare for product authorisation to keep your products on the market.

In this webinar, regulators, efficacy testing experts and regulatory consultants share practical insights on their experience and how to prepare.

Speakers:

  • CTGB (NL Competent Authority)

  • Eurofins (Testing laboratory)

  • Elements Advisory (Risk Assessment – ERA & HH RA)

Content:

  • Key differences between PT11 and PT12 use patterns

  • How to approach risk assessment (HH & ERA)

  • Efficacy testing strategies and expectations

  • Impact of the Review Programme on your timelines

  • Common pitfalls in PT11/PT12-related BPR dossiers

👉 Register now to learn how to succesfully prepare your PT11/12 BPR dossier

Please express your interest using the form below. Please note that this is not a binding step.