OcTech is formed by a group of highly-experienced medical device professionals, aiming to provide an integrated approach through our comprehensive expertise in clinical study design and protocol development, biostatistics, data management, regulatory consulting and medical writing.
  • Expert regulatory and clinical consultants to provide robust evidence development for regulatory submission and marketing
    • Providing strategic and operational support to medical device/IVD clinical studies
    • Average ≥ 12 years of experience in clinical research
    • Previously worked in Fortune 500 companies and academic research
    • Frequent interaction with FDA, China NMPA and other regulatory agencies
    • Extensive experience in collaboration with physicians for publications and presentations
  • Operational excellence through our global resources model to reduce costs and shorten project timelines.