The Provider Self Disclosure Protocol (SDP) and the OIG- Compliance: Self - Reporting to OIG - When should this happen and how to do it?

This training on OIG Self-Disclosure Protocol will help the attendees on the revised self-disclosure protocol (SDP), the process and procedures for self-reporting and the risks of not self-reporting. It will also review the need for the organization to be aware of excluded entities.

Recorded Version Only

(PPT + Recorded Streaming Link)

$249.00
1x Person - Unlimited viewing for 6 Months (For multiple locations contact Customer Care)
rec Recorded Link and Ref. material will be available in My Account Section
Last Recorded Date: Feb-2019

CD or USB Drive Only

(PPT + Recorded Training File)

$349.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days
Customer Care

Fax: +1-650-362-2367

Email: customercare@fdatrainingalert.com

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Areas Covered in the Webinar:
  • Is disclosure required? HHS says that often there is a legal duty or ethical duty to report violations.
  • The better question: Is there an advantage to self-reported disclosure?
  • Creates a presumption that a good, solid compliance program is in place
  • Can reduce monetary penalties
  • Provides flexibility in the return of any overcharges
  • Speeds up case resolution and management
  • Avoids corporate integrity agreements
  • What if I do not self-report, will things go hard on my facility?
  • Who can use the SDP?
  • What conduct or actions fall under SDP?
  • What conduct does not fall under SDP?
  • What must be submitted if a facility self-reports general violations?
  • What must be submitted in a case of false billing?
  • What must be submitted in a case involving an excluded person?
  • Eleven elements required.
  • Resolution of SDP matters.
Who Will Benefit: This webinar will provide valuable assistance to decision-makers in nursing homes, SNFs, medical offices, practice groups, hospitals, academic medical centers, insurers, business associates (shredding, data storage, systems vendors, billing services, etc.), such as:

  • Compliance directors
  • CEOs
  • CFOs
  • Administrators
  • Nursing managers
  • IT managers
  • Chief information officers
  • Health information managers
  • Healthcare counsels/lawyers
  • Office managers
  • Contract managers
Instructor Profile:
Laura S Hargraves Laura S Hargraves

Independent Business Owner, Bridging Documentation

Laura S Hargraves, MS CCC- SLP RAC-CT, has been working in all aspects of the healthcare industry for the past 30 years. Ms. Hargraves has been providing compliance and oversight of documentation to meeting changing guidelines during this period. She has a background in education, which helps her maximize her ability to communicate these changes to the various professionals that she works with. She is an expert in documentation/compliance/audits and reviews. Ms. Hargraves is also a professional presenter on topics related to Medicare, MDS 3.0, and documentation.

Topic Background:

In April of 2013, the Office of the Inspector General (OIG) of the United States Department of Health and Human Services issued new procedures called the SDP for facilities to self-report various violations. Knowledge of these procedures supports your team’s compliance goals. If there is a need for self-reporting, it indicates that your team’s compliance program is working.

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. FDATrainingAlert would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@fdatrainingalert.com call +1-888-771-6965 (Toll Free).

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