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Formazione >> Webinar e Formazione Online >> Information requirements for biocidal product authorisation: Part 1

Information requirements for biocidal product authorisation: Part 1

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FREE ONLINE WEBINAR: To continue supporting our customers' needs this webinar is dedicated to manufacturers only. To allow all interested companies attend, maximum two delegates form the same company will be admitted. Due to the type of event and limited audience capacity, participation of companies not included in this category will not be accepted. Attendance will be confirmed from the event's organizers.

DATE: October 25, 2023 | 3.00 PM - 4.00 PM CET

OFFICIAL LANGUAGE: English

SUBMISSION LINK: https://attendee.gotowebinar.com/register/7013005554280050780

ATTENDEES CAPACITY: 500 delegates

The event will be hosted within Go ToWebinar platform. Your registration request for this webinar will be submitted to the organizer for approval. You will receive information via email regarding your registration status.

Introduction

The Biocidal Products Regulation (BPR, Regulation (EU) 528/2012) concerns the placing on the market and use of biocidal products, which are used to protect humans, animals, materials, or articles against harmful organisms such as pests or bacteria, through the action of the active substances contained in the biocidal product. This webinar aims to provide a general overview of the information requirements to be included in the dossier for the authorisation of a biocidal product.

First, a brief overview of the Regulation will be given. The presentation will then focus on the parts of the Regulation dealing with the information requirements and their waiving, namely Annexes III and IV. Subsequently, we will understand the importance of guidance documents on biocide legislation and activities like data gap analysis and screening of Substances of Concern (SoC) and Endocrine Disruptors (ED) among co-formulants in biocidal products. Finally, a case study will be presented.

Agenda
  • Biocidal Product Regulation (BPR) – introduction
  • Information requirements and guidances
  • Screening SoC & ED
  • Case study
  • Lessons learned & take home message
  • Q&A
Speaker

Luca Romito is a Consultant in the field of chemicals, with a focus on biocidal products, at Eurofins Regulatory and Consultancy Services Italy.