Regulatory Affairs Consultant at ServiREACH specializing in REACH and CLP. I work on technical consultations and documentation to ensure regulatory compliance and enable the marketing of products in the EU.
Advanced Vocational Training Certificate in the manufacture of pharmaceutical, biotechnological and related products (Sep 2021–May 2023). UNED Chemistry (from Sep 2024).
I’m Jana Barnes, a Regulatory Affairs consultant at ServiREACH specializing in REACH and CLP. I help resolve technical queries related to the application and compliance of these regulations and transform regulatory requirements into key documentation to ensure smooth progress. I bring previous experience in Regulatory Affairs in the cosmetics industry, including the preparation of safety dossiers and the integration of technical information, as well as quality control and R&D/regulatory tasks in the chemical industry. On this page, I share practical articles on REACH and CLP, compliance criteria, and best practices for documentation for Regulatory Affairs, Quality, and Environmental teams.
Do you know what Annex XIV of REACH is and how to apply for an authorization? One of the key mechanisms of the REACH Regulation is Annex XIV, which includes substances that, due to the risks associated with their use, require prior authorisation to continue being used or placed on
The European Commission has approved hypochlorous acid as an active substance for use in type 1, 2, 3, 4 and 5 biocides. The approval date for PTs 2, 3, 4 and 5 is 01 July 2022 and 01 July 2021 for PT1s. (EU) Commission Implementing Regulation 2021/347 of 25 February
The content written by this author is based on their professional experience at Servireach. The information shared is for informational and practical purposes and does not replace professional legal advice when necessary.
