Clinical trial start-up, protocol development, study management, report writing and submissions for the following medical device indications: ischemic stroke; hemorrhagic stroke: aneurysm and vasospasm; heart failure; ophthalmology; urological surgery; peripheral vascular disease; mitral valve surgery; drug-eluting stents; women’s health.Development of European clinical business strategy – both pre-market and post-market within the commercial environmentClinical trial management from start-up to close-outCreation and fostering of relationships with key physician and site … READ MORE
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With European CE mark approval being essential to a robust global market, and with increasing demands on post market study requirements by Notified Bodies, a strong European clinical trial infrastructure is more critical than ever. For companies with … READ MORE
