Documentation of Clinical Risk Factors

Objectives:   * Attendees will better understand current concepts related to the documentation of intake data.
* Attendees will improve their informed consent processes.
* Attending doctors will be better prepared to document new clinical problems.
* Attending doctors will improve their records to benefit their patience and protect themselves in the case of litigation.

Description:   Dr. James Demetrious will provide a review of intake and informed consent documentation. Emphasis will be placed upon the documentation of clinical risk factors. He will discuss meaningful ways to improve the informed consent process and the means to improve clinical charting and communications to protect your practice and family.
Sponsor:   NCMIC
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