Eurofins BioPharma Product Testing Italy’s Post

There have been various changes to the RP since it was first introduced in the Review Programme Regulation (Regulation (EU) No 1062/2014) including two previous extensions. The most recent proposed extension presents a final deadline for all substances to be evaluated before December 31, 2030. To make this deadline achievable, the EU Commission, the Biocidal Products Committee (BPC), the MS CAs and ECHA have also identified a variety of actions intended to accelerate the progress of the RP. These proposed actions will have a significant impact on ongoing evaluations and introduce further regulatory deadlines that the Biocides industry must meet. Get insight into the proposed actions and regulatory deadlines here: https://lnkd.in/g5b3NtgX #BPR #BiocidalProducts #ECHA #BPC #BiocidalActiveSubstance #EUCommission #EU #BiocidalReviewProgramme

On November 21st, ECHA published their findings from the second enforcement action for the Biocidal Product Regulation. The report found that nearly half of all biocidal products evaluated are not fully compliant with either the BPR or the national regulations and that there are significant gaps in industry knowledge. In next week's Enforcement and the BPR webinar, we provide an overview of what enforcement is and who the Enforcement Forum are within ECHA. We will also provide a summary of the key outcomes of the first two BPR enforcement actions as well as an overview of the upcoming third enforcement action. To build your understanding of the outcomes of the Biocides Enforcement actions and to stay on top of the upcoming actions sign up for the webinar: https://lnkd.in/gynBw567 #enforcement #BPR #biocidalproducts #regulation #compliance #ECHA #webinar #YordasGroup

This is an upcoming webinar tomorrow on this very hot topic in the Biocides sector! 

Updates on Biocides! ECHA recently updated all supporting documents for applications under the BPR. Only the overview of Biocidal Product Family remains the same (last version:2021). When submitting an application under the BPR, remember that additional documents could be required besides the dossier itself. Always check the most updated templates on ECHA page https://lnkd.in/df7sRYMU #biocides #BPR #ECHA

Europe discovers 1 in 3 biocide products are non-compliant The national enforcement authorities in 29 countries checked over 3 500 biocidal products. Overall, 37 % of the checked biocides were non-compliant with at least one of the checked legal requirements. https://loom.ly/L3seIms #europe #enforcement #biocides

🚩Update of Supporting Documents🚩 ECHA has recently updated key supporting documents for applications under the Biocidal Products Regulation (BPR), with the exception of the Biocidal Product Family overview template. To ensure the smooth processing of your application, it is important to use the latest version of this template. Failure to do so may result in the rejection of your application. Stay informed and comply with the latest requirements. https://lnkd.in/eP33FFTP #ECHA #bpr #biocides #knoell

#biocides - Notify us by 31 January 2025 if you want to keep 𝘛𝘦𝘵𝘳𝘢𝘩𝘺𝘥𝘳𝘰-1,3,4,6-𝘵𝘦𝘵𝘳𝘢𝘬𝘪𝘴(𝘩𝘺𝘥𝘳𝘰𝘹𝘺𝘮𝘦𝘵𝘩𝘺𝘭)𝘪𝘮𝘪𝘥𝘢𝘻𝘰[4,5-𝘥]𝘪𝘮𝘪𝘥𝘢𝘻𝘰𝘭𝘦-2,5 (1𝘏,3𝘏)-𝘥𝘪𝘰𝘯𝘦 (𝘛𝘔𝘈𝘋) in the biocides Review Programme. Your action is needed, as companies have withdrawn their interest in getting the substance approved for uses in: ➡️ slimicides (product-type 12). #ChemicalSafetyEU #ChemicalSafety

📢 𝗘𝗻𝘃𝗶𝗿𝗼𝗻𝗺𝗲𝗻𝘁𝗮𝗹 𝗥𝗶𝘀𝗸 𝗔𝘀𝘀𝗲𝘀𝘀𝗺𝗲𝗻𝘁 : 𝗧𝗵𝗲 𝗻𝗲𝘄 𝗘𝗠𝗔 𝗚𝘂𝗶𝗱𝗲𝗹𝗶𝗻𝗲 𝗵𝗮𝘀 𝗯𝗲𝗲𝗻 𝗽𝘂𝗯𝗹𝗶𝘀𝗵𝗲𝗱! ➡ https://lnkd.in/eXHvSDcF 💊 The Environmental Risk Assessment (ERA) is a mandatory requirement when submitting a Marketing Authorisation Application (MAA). ✅ The new Guideline on the environmental risk assessment of medicinal products for human use recommends a double assessment to evaluate the potential impacts of active substances on the environment: 🔸 Risk Assessment 🔸 Hazard Assessment The new Guideline will be effective from September 2024. ➡ For more details on new recommendations, at CEHTRA, we answer your questions and provide guidance on new practices to follow. #pharma #EMA #guideline #environment #riskassessment

"One in three checked biocidal products found to be non-compliant EU-wide enforcement project found about 60 active substances in biocidal products that are not allowed on the EU, EEA and Swiss markets. One in three of the checked products did not comply with at least one of the checked legal requirements." #biocides #biocidi #health #safety #integratedpestmanagement https://lnkd.in/d5RkaSDM

⚡ Last week our EU Regulatory experts Koen Van Maldegem and Maud Grunchard were pleased to present an interactive webinar organised by Chemical Watch news & events by Enhesa, focusing on the myriad of potential regulatory issues to take into account when seeking authorisation for biocidal products in the EU. 💬 Koen and Maud were happy to answer a range of interesting questions from the audience, spanning the forthcoming BPR Refit, the anticipated amendment of the Review Programme Regulation, backlog dossiers, potential issues related to Mutual Recognition and Union authorisation. ❓ If you have questions related to the above topics or you are seeking assistance with any aspect of the EU product authorisation process, don't hesitate to get in touch! For more on our EU Regulatory practice, click here: #FieldfisherBelgium #EURegulatory #biocides #BPR #productauthorisation