Speakers


Susanna Mäentausta	Dr Rainer Otter	Poul Bo Larsen
Director, Product Stewardship & Regulatory Affairs, Kemira, Finland	Director, Regulatory Affairs, BASF, Germany	Chief Toxicologist, DHI, Denmark
REACH experiences and learnings in a medium-sized chemical company from 2010 towards 2018	Industry perspective on REACH registered chemicals suspected to be endocrine disrupting chemicals	Non-test methods, read across


Catherine Cornu	Dr Uta Herbst	Henrik Søren Larsen
Senior Scientific Officer, Dossier submission and PIC Unit; European Chemicals Agency (ECHA), Finland	Unit Chemicals Safety, German Federal Institute for Risk Assessment (BfR), Germany	Head of Chemicals Division, Danish Environmental Protection Agency, Denmark
Road to REACH 2018 – How ECHA can support your registration	Experiences on registrations in Germany - The REACH compliance project	What have we learned, what do we expect and how can we help you? From the perspective of a competent authority


Emma Jansson	Rikke Birgitte Bach	Marianne Lyngsaae
REACH Specialist, Swedish Paint and Printing Ink Makers Association (SVEFF), Sweden	Specialist, Corporate Environmental Management, Novo Nordisk A/S, Denmark	Quality System Manager, REACH Advisor, Brenntag Nordic, Denmark
Working with exposure scenarios at formulator level	A pharma perspective on authorisation	Management of ES information in SDS


Romualdo Benigni	Evgenia Stoyanova	Finn Pedersen
Administrator, (Q)SARs, Test Guidelines; Environment Directorate, OECD	Socio-Economic Analyst, Risk Management Implementation Unit, ECHA	Deputy Head of Chemicals Division, Danish Environmental Protection Agency, Denmark
The OECD QSAR Toolbox: a helpful tool to fill data gaps	Lessons learned on application for authorisation	Authorisations under REACH as a control measure


Hugo Waeterschoot	Julius Waller	Sigrídur Ingimarsdóttir
REACH Advisor, Eurometaux, Belgium and Industry Observer, the Member State Committee (ECHA)	Partner, EPPA, Belgium	General Manager, Regulatory Affairs; Haldor Topsøe A/S, Denmark
Authorisation under REACH: How to best anticipate or prepare for authorisation with special attention to SME’s	Experience in authorisation for producers and downstream users	Industry strategies for 2018 registrations


Jerker Ligthart	Heidi Morka	Franziska Kramer Birkved
Senior Chemicals Advisor; ChemSec, International Chemical Secretariat, Sweden	Head of Section, Chemicals; Norwegian Environment Agency, Norway	Senior Scientist; Novozymes, Denmark
How to use the SIN List and SINimilarity as tools in a proactive substitution work for SVHC substances	Use of registration data and exposure scenarios in regulatory co-operation and enforcement	Registration of enzymes as UVCB – respiratory sensitizers and exposure scenarios


Mikael Poulsen	Dr Torsten Funk
Programme Manager, Partnership for Substitution of Harmful Chemicals	Regulatory Compliance Manager Chemical Safety, Sika Services AG, Switzerland
Partnership for substitution of harmful chemicals: Objectives and results	Safe end use of products under REACH - a formulator's perspective