It can be difficult to navigate the nuances of REACH registrations for both your registrations and re-registrations, which can be essential to avoid lost time and money. 

A selection of Extended One Generation Reproductive Toxicology studies (EOGRTS) have recently been reviewed by ECHA (the European Chemicals Agency). The Agency identified seven critical issues in the design and conduct of these studies under OECD Test Guideline 443. 

Register for our upcoming webinar to hear our in-house DART and regulatory experts discuss these issues.  

If you are unable to join us on the day, be sure to register to access the on-demand webinar recording.  

DATE
Thursday, November 4, 2021
11:00 AM – 12:00 PM EDT (4:00 PM – 5:00 PM CET)

REGISTRATION
https://www2.criver.com/l/60962/2021-10-18/jpm3kn