Modular Solution for Cosmetics Compliance
Check the Conformity of your Formulas
Secure your regulatory documents for each zone
Optimize on-site risk management
Manage your Safety Data Sheets efficiently
Automate your regulatory monitoring
Ensure the traceability of your substances
Maintain good HSE risk management
Managing cosmetic regulatory data across the U.S., Canada, and Europe is no longer just a compliance issue. It is a data management challenge that directly impacts consistency, risk, and scalability for cosmetic brands.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
ECHA's report highlights a growing trend in using alternatives to animal testing for chemical toxicity, with increased implementation of read-across and in vitro methods. This aligns with REACH's goals and is notably advancing in Vietnam with government support.
The Biocidal Products Regulations (BPR) EU No. 528/2012, effective from September 2013, replaced the French Directive No. 98/8 EC. It introduces new provisions like data sharing and Union authorization, aiming to enhance human and environmental protection and simplify marketing authorization.
This guide offers technical advice on BPR obligations for active microorganisms and biocidal products, covering identification, effectiveness, and impact on humans, animals, and the environment. It replaces previous guidance documents, aligning with Annex II and III of the BPR.
Learn about the key changes in WHMIS 2015, aligned with GHS, including hazard classification, SDS requirements, labeling, and enforcement. Stay compliant with the key dates provided.
"Certibiocide" is a personal certificate for individuals handling biocides, requiring a 3-day training. It applies to specific biocide types and is valid for 5 years. Companies must comply with certain obligations, though no direct sanctions are specified for non-compliance.
This blog provides an overview of the regulatory processes and costs associated with obtaining marketing authorisation for biocidal products in the EU, including national, mutual recognition, and EU-wide authorisations. It also details the specific fees set by the French government for various authorisation evaluations.
