Porta Medica provides complete regulatory services for medical device manufacturers, from clinical trials, through conformity assessment (CE-marking) to post-market clinical follow-up and PMS. We have experts in the field of biocompatibility assessment, clinical trial, risk management, QMS, lawyers and experts in other areas. Porta Medica also provides support to manufacturers in setting regulatory strategy as part of the company's strategy. Not every medical device brings potential to unmet clinical needs and trade. But any medical device that targets unmet clinical needs and has business potential we are able to bring to EU market. Be with us in the EU market faster than the competition.