14 Imber St.
MedicSense assists Medical Devices manufacturers dealing with clinical, regulatory and QA requirements. We provide technical and regulatory services from early stages of the product to certification (FDA, CE etc.), design pre-clinical/clinical trials, CRO activities, establishment of QMSs, Israeli Registration Holder, EAR, U.S. Agent and Standards Review. MedicSense is comprised of a highly competent multidisciplinary team. Our strengths are based on our extensive engineering, techno-regulatory background and experience with a wide range of technologies. We know how to get products past the regulatory hurdles providing pragmatic solutions. We understand the needs of the vibrant high tech medical device industry and the dynamic regulatory environment.