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Speaker Guidelines

Statement of Purpose: The speaker agrees that the CME activity is for scientific or educational purposes. Any discussion of a company's products will be objective, balanced, and scientifically rigorous.

Technical Assistance: Speakers may seek limited technical assistance from commercial supporters in preparing slides or audiovisual materials but must not let the company influence the content of the program.

Limitations of Data: The speaker must disclose any limitations on the information that is presented, such as data that represent ongoing research, interim analysis, preliminary data, or unsupported opinion.

Discussion of Unapproved Uses: If unapproved (unlabeled) uses are discussed during the CME activity, the speaker must disclose that the product is not approved in the United States for the use under discussion.

Opportunities for Debate: During the CME presentation, the speaker will open the floor for scientific debate or questioning.

Content Validity: Speakers must assure that any clinical recommendations made are valid for use in the care of patients by completing and signing the attestation form. All scientific research referred to, reported in, or used in CME in support or justification of a patient care recommendation must conform to the generally accepted standards of experimental design, data collection, and analysis. The following must be adhered to:

  • Clinical care recommendations must be based on evidence that is accepted within the profession of medicine as adequate justification for their use
  • All the recommendations involving clinical medicine in a CME activity must be based on evidence that is accepted within the profession of medicine as adequate justification for their indications and contraindications in the care of patients
  • A recommendation on clinical care must be more than firmly held beliefs or hopes for efficacy
  • Data or information accepted within the profession of medicine must support the recommendation
  • The conclusions drawn from the data must be those that would be reasonably drawn from those data

The validation of clinical content does not mean that every clinician in the country accepts the recommendation or that the recommendation is part of FDA-labeling. An important part of validity is the scientific integrity of the data from which the conclusions are drawn and the clinical recommendations crafted.

Conflict of Interest: The CME program's policy to identify and resolve conflicts of interest is drawn from the School's Conflict of Interest Policy adopted November 2008. An individual who refuses to disclose relevant financial relationships will be disqualified from being a planning committee member, a teacher or an author of CME and cannot have control of, or responsibility for, the development, management, presentation or evaluation of a CME activity.

For more information: Individuals involved in CME events are encouraged to visit National Faculty Education Initiative web site to take a free 30-minute tutorial on eliminating commercial bias from CME presentations.

Another resource for information for those who plan and participate in CME and improvement programs is the Association of American Medical Colleges (AAMC). The AAMC CME web site is a guide to employ best educational methods of quality improvement and performance improvement principles to close the clinical care gap.


For more information, contact:
Karen Bertke, CME Program Administrator
E-mail: karen.bertke@wright.edu
Phone: 937-775-3435
Fax: (937) 775-3256

Mailing address:
Office of Faculty and Clinical Affairs
Boonshoft School of Medicine
Wright State University
P.O. Box 927
Dayton, OH 45401-0927

Location: University Park
3817 Colonel Glenn Hwy.
Fairborn, OH 45324