Visit MakroCare at Booth #8 in the upcoming 2nd European Symposium on The New Agreed Regulations on Medical Devices – (RMD2017) which will take place 16-17 October 2017, at the Hilton Berlin in Berlin, Germany.
Major topics that will be covered during this conference includes, new Regulations strengthening the rules on placing medical devices on the market, reinforcement surveillance, manufacturers’
responsibilities for the follow-up of the quality, performance and safety of their devices and the improvement trace-ability throughout the supply chain
MakroCare has successfully assisted many Pharma, Biotech and Device companies’ right from designing their Regulatory Strategy to getting product approvals globally. We have been managing
more than 4000 Regulatory submissions (Clinical, Market Authorization and Post Market Maintenance Applications) annually. Our functional services include Strategy & Consulting, Regulatory
Services, Labeling, Submissions, Reg Ops, Development(CPC Cenmon), Medical Risk Management/Safety & Medical Affairs, Technology (Products & Solutions)