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Understanding Exclusions from Participation in Federal Health Care Programs
2/12/2015 10:00 AM - 11:00 AM
online event Fremont, California United States
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Summary:

Overview: OIG was established in the U.S. Department of Health and Human Services (Department) to identify and eliminate fraud, waste, and abuse in the Department's programs and to promote efficiency and economy in Departmental operations. OIG carries out this mission through a nationwide program of audits, inspections, and investigations. In addition, the Secretary has delegated authority to OIG to exclude from participation in Medicare, Medicaid, and other Federal health care programs Persons that have engaged in fraud or abuse and to impose civil money penalties (CMPs) for certain misconduct related to Federal health care programs.

The effect of OIG exclusion is that no Federal health care program payment may be made for any items or services furnished (1) by an excluded person or (2) at the medical direction or on the prescription of an excluded person.

The exclusion and the payment prohibition continue to apply to an individual even if he or she changes from one health care profession to another while excluded. This payment prohibition applies to all methods of Federal health care program payment, whether from itemized claims, cost reports, fee schedules, capitated payments, a prospective payment system or other bundled payment, or other payment system and Applies even if the payment is made to a State agency or a person that is not excluded.

Webinar On Risk Management and RiskBased Monitoring
2/2/2015 1:00 PM - 2:00 PM
Online Mississauga Canada
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Summary:

This course provides an understanding of risk management principles and makes the links between study level risk management and the implementation of risk based monitoring.

Webinar On The FDA 510k and QSubmission Best Practices
2/4/2015 1:00 PM - 2:00 PM
Online Mississauga Canada
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Summary:

This webinar will provide an opportunity to get familiar with an FDA's process to communicate with the industry early in the process for sustainable 510(k) preparation and submission.

Webinar On The FDA Medical Device Approval Process Preparation of 510ks IDEs PMAs
2/5/2015 1:00 PM - 3:00 PM
Online Mississauga Canada
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Summary:

This web presentation presents an overview of the requirement to obtain FDA permission to market a Medical Device products.

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