Product registration/ notification (cosmetics, biocides, medical devices, detergents, preparations) with German authorities and EC foreign authorities.
Creation of safety assessments (Safety Report) and product Information files (PID) for cosmetics according to the requirements of the new Cosmetics Regulation 1223/2009 Annex I.
Coordination with the authorities and notified body for medical devices.
Risk analysis for medical devices according to DIN EN ISO 14971:2007
Technical documentation for medical devices according to 93/42/EEC and EN ISO 13485
Creation of supplier questionnaires. Product safety.
Interim Management (Cosmetics, REACH, Product Safety, Research & Development, Quality Management)