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
Learn about the risks of non-compliance with the new medical devices regulation in Europe, including financial losses, damage to brand image, and sanctions by Member States. Understand evolving obligations and how to ensure compliance to avoid these risks.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Navigate the new Medical Device Regulation with ease. Discover changes in classification, roles, and compliance to ensure safety and transparency in Europe.
Discover the key changes in the EU Medical Devices Regulation, its impact on classifications, compliance deadlines, and implications for businesses.
Ensure your medical devices comply with Regulation (EU) 2017/745. Learn about certification deadlines and requirements for new and existing devices.
