Medical Writing- CRI006

High-quality medical writing has a multi-million dollar impact on a company’s financial performance. It can prevent the need for additional clinical trials which are often required because of unclear communication and poorly written documents.  Good medical writing can lead to optimal product labeling, allowing successful product promotions and maximization of advertising claims.

Well-written submission documentation can decrease the length of the product marketing approval process and increase the amount of time a product can be sold under patent protection. 

The Medical Writing program offered by Clinwell will give participants comprehensive insight into proper medical and technical writing, as well as what regulatory agencies look for in compliant documentation, submissions and product marketing. Upon completion of this certification, participants will know the fundamentals of effective writing in the regulated environment and be more effective overall

communicators.   This course is valuable to those who write or review documentation in support of clinical trials and regulatory submissions, those who prepare or review articles and abstracts about therapeutic products in any phase of development for professional publication or those new to the discipline and wish to understand the scope of medical writing. Typical attendees include medical writers, reviewers of medical documents, clinical research managers and associates, regulatory affairs professionals, project physicians and medical monitors.