Ali Mirtaghavi

Mdr Clinical Specialist Medical Writer @Convatec

Conducting clinical evaluation workflow for Class I, IIa, IIb and Class devices - Author regulatory documents such as CEP, CER, CEM, PSUR, PMCF, PMS plans, SSCP and Clinical Development Plan - Responsible for conducting clinical evaluation plan and report, as well as ensuring compliances of ostomy and continence care medical devices with MDR (EU)/2017/745 regulations-Specialist in literature search optimization for Medical Device Evaluations, sources of data for State of the Art, benchmarking devices and equivalent devices- Defining performance, safety and adverse event endpoints, using degrees of separation from PICO framework with text mining.