OcTechis 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.