Introduction
The REACH Regulation requires companies to submit registration dossiers for substances they manufacture within or import into the EU in quantities of one tonne or more per year. Upon submission, the European Chemicals Agency (ECHA) assigns registration numbers. Following this, ECHA evaluates the dossiers, which includes conducting compliance checks and examining testing proposals to ensure the quality and adequacy of the submitted data. Based on these evaluations, ECHA issues decisions that registrants must comply with.
In this webinar, we will briefly introduce updates on registrations under EU REACH, explain how authorities evaluate dossiers, and provide advise on how registrants can ensure compliance during dossier evaluation and meet REACH requirements.
Time
Language | Date | Time | Speaker | Registration |
English | March 27 2025 | 3pm (GMT+8, Beijing Time) | Yolanda Zhang | |
4pm (GMT+1, Central European Time) | Adam Hembrecht | |||
1pm (GMT-4, US Eastern time) | Lucy Wang |
Registration Fee
Free
Main Contents
- Brief introduction to EU REACH;
- Global REACH registration statistics;
- Evaluation status; and
- Strategies for compliance under evaluation and case analysis.
Speaker
Yolanda Zhang, Chemical Regulatory Consultant, CIRS China
Yolanda obtained her Master's Degree from Leeds University and has been working for several years at the CIRS Group as a senior regulatory consultant. She specializes in global chemical regulations, including China REACH, EU REACH, Global GHS, and K-REACH, and has provided professional regulatory consultancy services to numerous enterprises.
Adam Hembrecht, Junior Regulatory Consultant, CIRS EU
Adam is a junior regulatory consultant from CIRS EU based in Dublin, Ireland. He mainly focuses on the chemical regulations in the EU and UK. He graduated from Dublin City University (DCU) with honours in 2016 holding a Chemical and Pharmaceutical Science degree. He continued in academia, carrying out an MSc through research in the Stability of Peptide cross-linkages in Monoclonal antibodies with Technological University Dublin (TU-Dublin Tallaght). Following this he spent a year in the Quality department of the largest contract development and manufacturing organization (CDMO) in Ireland ensuring the quality of raw materials for pharmaceutical processes.
Lucy Wang, Chemical Regulatory Consultant, CIRS USA
Lucy graduated from George Washington University with a Master's degree in Environmental and Green Chemistry. She has been researching chemical regulations in different countries and is responsible for the US market at CIRS. Lucy helps to serve enterprises with professional regulatory compliance consultancy.
Registration
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Contact us
Chemical Inspection & Regulation Service (CIRS)
Addr: 11/F., Building 1, Dongguan Hi-Tech Park, 288 Qiuyi Road, Binjiang District, Hangzhou 310052, China
TEL: +86 571 8720 6574
Email: service@cirs-group.com