In this webinar we provide a high-level overview of the underlying principles of the efficacy assessment, outline the details of what resources applicants can use to meet the requirements and advise on some best practices to follow.

This webinar aims to enhance understanding of an exemption where the substance is used solely for product and process-orientated research and development (PPORD).

This webinar aims to enhance understanding of the evolving regulatory environment for chemical management in South America.

This webinar aims to enhance understanding of the evolving regulatory environment for chemical management in South America.

In this webinar, the chemistry and biocidal activity of BKC is briefly discussed in addition to the current regulatory status under the biocidal products regulation (BPR).

Gain practical insights into exemptions and understand the precise domain of applicability under each regulation. Whether you're navigating FIFRA, TSCA, or FD&CA, this session equips you with essential knowledge for successful registrations.

In this webinar, we will provide an overview of the changes to the WHMIS Regulations. We will delve into key aspects such as the updated SDS requirements, new classification endpoints, changes to improve clarity and precision of Hazard Communication and how this will impact your supply chain. Join us as we navigate the intricacies of WHMIS and equip you with the knowledge needed for a seamless transition.

This webinar will summarise the amendments to KKDİK, and detail the impact on pre-registrations, registrations, SDS and other supply chain obligations. We will provide updates on actions taken by the Ministry to improve the process and finish with recommendations on complying with the new deadlines.

Sign up for this introductory webinar for insight into the fundamental principles of SSbD and how they can be incorporated into product design without extensive disruption.

On November 21st, ECHA published their findings from the second enforcement action for the Biocidal Product Regulation. In this webinar, we provide an overview of what enforcement is and who the Enforcement Forum are within ECHA.

Stay up-to-date with the latest developments in chemical classification and labelling as we dive into the revised CLP (Classification, Labelling, and Packaging) Regulation

This webinar has been developed in response to ECHA - in coordination with various EU member states, publishing the results of the first EU-wide Treated Article Enforcement Action. Sign up for more insight.

This webinar focuses on the 2023 deadlines for REACH-like regulations in Asia Pacific. We will provide attendees with a brief overview of the regulatory background, and summarise key actions required in 2023.

This webinar has been developed in response to the development of a new initiative, the product environmental footprint (PEF), which when launched is expected to have global implications.

The CLP regulation offers alternatives to the different market players to encourage and facilitate the notification of their products. Learn about the submission alternatives in this webinar.

Learn about the difference between sustainability and ESG frameworks and standards and how they’re linked to supply chains.

This webinar is to help companies understand the requirements of Article 89 of the Biocidal Product Regulation (BPR) transitional measures and the diversity of national transitional procedures.

This webinar gives insight into products that can be included together in a family and gives a brief overview of the Dossier preparation and submission process.

This webinar will cover the current UK-REACH Registration model and the steps that companies may need to take in order to register existing and new chemicals.

The registration deadline for Turkey REACH (KKDIK) is a few months away and there are still a large proportion of substances without any Lead Registrants appointed.

This webinar provides insight into the LCA, an internationally recognised tool used to quantify the potential environmental impacts of products (goods and services) throughout their life cycle.

Learn how phasing out and managing PFAS for specialized applications will be imperative for the industry in the future.

The Turkey REACH (KKDIK) registration deadline is fast approaching. By 31 December 2023, all companies manufacturing/importing substances ≥ 1 tonne/year in Turkey must have registered their substance.

In this webinar, we will introduce the concept of borderline products, give an overview of the affected regulations and explain the compliance challenges associated with these products.

This webinar has been developed in response to ECHA’s new update to its efficacy guidelines. Several significant changes have been made to the efficacy guidance, impacting the data requirements applicants need to provide for their BPR product authorisation dossiers.

Find out more about the PPORD exemption and how to submit a PPORD Notification to ECHA or the HSE.

This webinar focuses on the 2023 deadlines for REACH-like regulations in Asia-Pacific.

Learn about the similarities, differences and challenges of using KKDİK tools to prepare for the registration deadline.

This webinar gives an overview of the cosmetic regulations in the European Union and some of the requirements.

This webinar will provide guidance on how to check your obligations and how to create a roadmap for K-REACH compliance.