GAP analysis for the transition to MDR 2017/745)
Clinical Evaluation Tools
Critical evaluation of scientific literature (All Classes)
Clinical Investigation (Class III / Implantable Device)
Clinical Evalutation Report
Post Market Surveillance Tools (PMS Plan, PMS Report, PMS Safety Update Report, Eudamed Update, )
Post Market Clinical FollowUP Tools (PMS Plan, PMS Report, PMS Safety Update Report, Eudamed Update, )
Easy to keep in contact with the manufacturer
Easy tools to share and kept a feedback with your customers (i.e: Medical Doctors)
Easy tools for custom survey using artifical intelligence (AI) and innovative instrument (i.e: Robot phone call and chat-in)
Easy dashboard to watch video, datasheet from the manufacturer of medical devices always update
Easy to keep in contact with the manufacturer
Post market Surveillance easy to do online
Easy tools to share and kept a feedback with your customers using online survey
Easy tools for custom survey using artifical intelligence (AI) and innovative instrument (i.e: Robot phone call and chat-in)
The MDR platform is the first platform to help manufacturer, distributor and medical doctors with the new requirements according to MDR 2017/745. The tools will help you to simply the process, to improve your business, to keep business informations from your data.
