Course Development: Intermediate Medical Writing, Devices

We are looking for an experienced subject matter expert (SME) to develop our Intermediate Medical Writing: Medical Devices course with the most up to date regulations and practices.This course will provide an overview of some of the more complex documents prepared by regulatory and medical writers, including key sections of the Premarket Approval, Premarket Notification applications and PostMarket for medical devices. It will introduce the components of each of these documents and teach techniques for improving document quality in order to advance regulatory writer careers.