

Overview: PSUR, as outlined in Article 86 of the MDR and Article 81 of the IVDR, is a critical document that provides comprehensive information on the safety,


For medical device manufacturers aiming to comply with the European Union Medical Device Regulation (EU MDR 2017/745), a robust “State-of-the-art” (SOTA) section is crucial for demonstrating clinical


Our Cosmetic Responsible Person team have recently received a number of queries from clients regarding the use of QR codes on their cosmetic product labelling. “Can a


The EU Regulation 2023/1545 amends EC Regulation 1223/2009 on the labelling of Fragrance Allergens in Cosmetic Products. The EC Regulation 1223/2009 on Cosmetic Products contains a list