Velferd, and in particular its brand VLF Consulting, is an innovative multi-services hub supporting companies in the development of new ideas and solutions in pharmaceutical world, with a strong focus on Regulatory Affairs and Quality Assurance aspects. MEDICAL DEVICES Quality System implementation according ISO 13485 and FDA 21 CFR 820 CE Marking Technical Documentation according to MDR 2017/745 US market: FDA Registration, Establishment Registration and Listing US market Design Control Risk Management and Usability Clinical Evaluation and Clinical Studies Biocompatibility Evaluation according to ISO 10993:2018 Post-market Surveillance Design and Development Testing partner FOOD SUPPLEMENTS AND COSMETICS Technical Dossier creation and maintenance Product Design and Development Raw material research and selection Supplier and production site evaluation SPECIFIC TRAINING IN-HOUSE or ON THE JOB