Dieses Webinar soll Ihnen helfen, Ihre Rolle in der Lieferkette zu erkennen, Ihre Verpflichtungen zu identifizieren und Sie auf die KKDIK, CLP und SDB Gesetzgebungen in der Türkei vorzubereiten.

Since the Turkey’s KKDIK regulation came into force on 23 December 2017, companies have been pre-registering their substances in advance of the 31 December 2020 pre-registration deadline. In addition, notification is required under the Turkey Classification, Labelling and Packaging (CLP) (also known as SEA) regulation, and Turkish SDS require special certification by a certified SDS expert in order to guarantee compliance.

GRMS2 is a powerful regulatory database and monitoring service for the automotive and related industries, created by Yordas Group in conjunction with ACEA. The focus of this webinar is to showcase how users can get the most out of GRMS2, as well as what reports can be created for horizon scanning purposes, maintaining sight on upcoming regulations that may affect your business.

This webinar will address the recent 2020 updates to CDR that were not part of CDR 2016. In addition, we will discuss how to prepare for CDR, who needs to comply, and what information is required

As we move into the latter half of 2020, it is time to revisit your obligations to comply with Commission Regulation (EU) 2017/542, amending CLP Regulation 1272/2008.

In 2017, the Eurasian Economic Union (EAEU) published a Technical Regulation called EAEU TR 041/2017 (commonly known as “Eurasia REACH”).

Neue Stoffe müssen aufwendig registriert werden, für bestehende Stoffe sind Aufwand und Datenanforderungen geringer. Dieses Webinar fasst die Anforderungen an die Nominierung in Russland zusammen

Do you have customers or entities in Taiwan? This webinar will help you identify your industrial obligations under the new TCCSCA with emphasis on “existing substances”

Endocrine disruptors have recently been the focus of regulatory action in the European Union (EU) due the impact of these substances on human health and the environment. Specific provisions on how to evaluate and assess endocrine disruptors were recently included in several pieces of EU legislation. The purpose of this webinar is to review the requirements related to Endocrine Disruptors in the EU in 2020, look at the criteria to identify them, and discuss the limits of the assessment process.