Visit MakroCare in the upcoming 12th Semi-Annual IVD Clinical & Regulatory Affairs Conference which will take place at Arlington, VA on October 22-23 2019.
Major topics that will be covered during this conference include, Considerations while Navigating Regulatory Pathways for Novel IVD Tests, Companion Diagnostics, & Precision Medicine,
Addressing Clinical Trial Design & Validation of Technological Advancements, with Insights on Challenging International Regulations including EU IVDR & Asian Regulatory Pathways.
MakroCare has successfully helped many Medical 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, EU MDR and IVDR
Services, Labeling, CER, UDI, Post Marketing and Data Solutions. Makrocare presents keys to successfully mastering the new MDR & IVDR.