ComplianceOnline

Medicare and Medicaid EHR Incentives for Eligible Professionals & Hospitals

Instructor: Kosta Makrodimitris
Product ID: 702818
Training Level: Basic to Intermediate
  • Duration: 90 Min

recorded version

$229.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Apr-2013

Training CD

$299.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This training will help you understand the Medicare and Medicaid Electronic Health Records (EHR) Incentive Programs that are offered to eligible professionals and hospitals from the federal government across the states.

Why Should You Attend:

This training will provide the new and expected stages and policies for Medicaid/Medicaid EHR Incentives and discuss their effects across the states and the industry. It will explain what the policies are, predict coming regulations and discuss how the industry (vendors) will be affected. We will explore relevant regulations and standards in the US and globally.

All groups and professionals who have responsibility or need to understand the basics of Medicaid/Medicaid EHR Incentives should attend.

Areas Covered in the Webinar:

  • Overview of Medicare and Medicaid EHR Incentive Program
  • Background for EHR and current landscape
  • Overview of Meaningful use for EHRs
  • Health Information Exchanges (hospitals, professionals and states)
  • Choosing a Program: Medicare or Medicaid?
  • Stage 1 Qualification and Compliance
  • Stage 2 Qualification and Compliance
  • Clinical Quality Measures and EHRs
  • Future of Health Exchanges and EHRs

Who will Benefit:

  • Compliance Officers
  • Privacy Officers
  • Health Information Managers
  • Medical Office Managers
  • Legal Counsel
  • Operations Directors
  • Information Security Officers
  • Compliance Officers
  • Privacy Officers
  • Information Technology Managers
  • Clinical operations teams
  • Clinical data management groups
  • Biostatisticians
  • Medical Writers
  • Medical Doctors
  • Standards experts
  • Medical Office Managers
  • Senior Management
  • Clinical research leaders & members
  • Clinical Scientists
  • Regulatory affairs
  • Medical offices, Hospitals, Health Insurers

Instructor Profile:

Dr. Kosta Makrodimitris, PhD, CF-FDA, CP-EHR, is Biomedical/Health Informatics Advisor, Author & Strategist. He is the principal for K Makrodimitris that specializes in Health IT & BIO business development, eHealth education, Health Information policy. He is certified on EHR/PHR, Clinical Trials, Biotech/Drug Development, and trained in US FDA/DHHS laws, regulations (devices, foods, drugs, personalized health). He is involved as:

  • Medical Devices Committee Member, Writer at The Food and Drug Law Institute
  • Consultant (Health Informatics/Policies/Standards) at DHHS/ONC, Standards & Interoperability Health Information Management Systems Society, Health Level 7(EHR, Genomics, mHealth) , small businesses
  • Nifty-Fifty Nominee nationwide, Speaker, Volunteer at USA Science Festival His multifaceted area of work is in health technology, architecture, policy and decision making.

In academia (Johns Hopkins, University of Virginia), Kosta researched and published articles in archival journals concerning biomedical and chemical informatics. In industry (FannieMae, Sysco, MAKROnanoKosmos), Kosta designed systems, managed analytics projects, cofounded eHealth business contributing to solutions (foods, health, finance). In government (US-FDA/DHHS Commissioner's Fellow), he worked in regulatory science, enterprise architecture, standards & policy in public health. In MD State he was program manager for BIO-economic development. LinkedIn Profile: http://www.linkedin.com/in/kostamakrodimitris

Follow us :
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada
Computer System Validation - Reduce Costs and Avoid 483s

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. ComplianceOnline 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@complianceonline.com call +1-888-717-2436 (Toll Free).

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