Skip to main content

HIPAA Compliant Fundraising Under New Rules - 2019

Compliance Key -  Hipaa Compliance Training

HIPAA Compliant Fundraising Under New Rules - 2019


Joel Simon
Joel Simon is one of the nation's leading experts on the fund raising aspects of HIPAA. Joel has been a member of the Maryland bar for 30 years, and his professional experience includes work as the assistant general counsel of a community hospital. Joel is an editor of "Fundraising Under HIPAA" published by the Association of Fundraising Professionals. He has lectured on Fund Raising under HIPAA to national audiences since the original HIPAA regulations were first proposed 17 years ago.
Overview
Not-for-Profit organizations that are governed by HIPAA often need or want to fund raise from their patients, clients, or families. What protocols should be in place to maximize philanthropic opportunities under HIPAA? What compliance measures need to be in place and assessed to properly use protected health information for fund raising.
Why should you attend this webinar?
Institutions that fundraise and have access to of HIPAA protected health information need to be aware of opportunities to hone fund raising strategies to maximize philanthropic revenue for your organization.
Similarly, health related institutions that fund raise must make sure their fundraising practices minimize the compliance risks and satisfy mandates governing the use of patient/client information.
If you are a health care professional who is affiliated with a fund raising institution, you will learn how you can remain both ethically and legally complaint with patient privacy, while assisting both your affiliated institution and your patient/client. 
Institutions will learn about compliance requirements for donor data base management. You will also learn effective and efficient strategies to maintain compliance.
You will learn how to keep your fund raising communication and related policies compliant without impairing operational effectiveness.
Areas Covered in the Session:
  • HIPAA and Fundraising Overview
  • Compliance Requirements
    • Notice of Privacy Practice
    • Opt-out language - what and when
    • Data Base issues
  • Strategies for using health information
    • Clinician engagement
    • Prospect pool segmentation
    • Major Gift strategies
Who can Benefit:
  • CDO and other development staff
  • CDO and IT compliance staff
  • General Counsel and general compliance staff
  • Physician leaders (CMO, department chiefs, division heads)
  • Administrative department heads
  • CNO and other clinical leaders

Labels:
Location: United States

Comments

Post a Comment

Popular posts from this blog

New 2019 HIPAA Guidance on De-Identifying Protected Health Information

Compliance Key  -   HIPAA Compliance Training Overview This seminar will be addressing how practice/business managers or compliance officers need to get their HIPAA house in order, as HIPAA is now fully enforced and the government is not using kid gloves anymore. It will also address major 2019 changes taking place with the Health and Human Services regarding the enforcement of the HIPAA law as well as detailed discussions on the Phase 2 audit process and current events regarding HIPAA cases (both in courtrooms and from real-life Audits). Our instructor - Mr. Brian Tuttle  has over 20 years of experience in working as Compliance auditor and has been an expert witness on multiple HIPAA cases. He`ll thoroughly explain on HOW and in WHAT scenarios patients can claim for cash remedies. More importantly, Brian will show you how to limit those risks by simply taking proactive steps and utilizing best practices. Why should you attend this seminar? This Sem...
Post a Comment
Read more

Classifying Medical Devices in US and EU

Compliance Key INC  -  Healthcare Compliance Webinars Overview The Food and Drug Administration (FDA) has established classifications for approximately 1,700 different generic types of devices and grouped them into 16 medical specialties referred to as panels. Each of these generic types of devices is assigned to one of three regulatory classes based on the level of control necessary to assure the safety and effectiveness of the device.The determination process, how you apply the classification process to your device, is complex and requires several levels of analysis to make the proper device classification. Proper medical device classification is the fundamental first step in submitting your device for approval anywhere in the world. This webinar will detail the medical device classification process for the United States through the FDA and will overview the very complex process for medical device classification within the EU. Specifically, this webinar will provid...
Post a Comment
Read more