Visit MakroCare in the upcoming 10th Annual EU Medical Device Clinical Research Conference which will take place at Berlin, Germany on March 20-21, 2018.
Major topics that will be covered during this conference includes, aligning clinical strategies with MDR & MEDDEV Regulatory Requirements, obtaining a greater volume of clinical data to
support Regulatory & Access Goals, integration of unique initiatives such as IIS to broaden indications & maintain budgets
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)