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HIPAA Professional 2018 - HIPAA Compliance Officer Training | HIPAA Professional 2018

Date2018-02-08 - 2018-02-09

Deadline2018-02-07

VenueWashington, DC, USA - United States USA - United States

KeywordsHIPAA Training; Plasma Drug Levels; Compliance Officer

Websitehttp://www.globalcompliancepanel.com/con...

Topics/Call fo Papers

Overview:
This lesson will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order as HIPAA is now fully enforced and the government is not using kid gloves any more.
It will also address major changes under the Omnibus Rule and any other applicable updates for 2018 and beyond.
There are an enormous amount of issues and risks for covered entities and business associates these days.
I will speak on specific experiences from over 17 years of experience in working as an outsourced compliance auditor, expert witness on multiple HIPAA cases, and thoroughly explain how patients are now able to get cash remedies for wrongful disclosures of private health information.
More importantly I will show you how to limit those risks by simply taking proactive steps and utilizing best practices.
We will go into detail on the highest risk factors and how they commonly occur
Why you should attend:
The HIPAA Omnibus Rule has changed the HIPAA landscape for good!
This once rarely enforced law has changed and you need to know what's going on!
What are the new roles and responsibilities for compliance officers?
Protect your practice or business!
These day's trial attorney's pose a higher risk than the Federal government!
State laws are now in place increasing liability for patient remedies!
What factors might spurn a lawsuit or a HIPAA audit? ...are you doing these things?
Why are the Feds enforcing after all these years?
We will be discussing 2018 changes taking place in Washington with the Health and Human Services in regards to the enforcement of the HIPAA laws already on the books as well as some detailed discussions on the audit process as well as some current events regarding HIPAA cases (both in courtrooms and from live audits)
Areas Covered in the Session:
• History of HIPAA
• HITECH
• HIPAA Omnibus Rule
• How to perform a HIPAA Security Risk Assessment
• What is involved in a Federal audit and how is it conducted
• Risk factors for a federal audit
• EHR and HIPAA
• Business Continuity/Disaster Recovery Planning
• Business Associates and HIPAA
• In depth discussions on IT down to the nuts and bolts
• BYOD
• Risk factors that can cause an audit (low hanging fruit)
• New rules which grant states ability to sue citing HIPAA on behalf of a patient
• New funding measures
• ..much, much more
Who will benefit:
• Practice Managers
• Compliance Officers, and any business associates privy to private health information and under the auspices of this law
Agenda:
Day 1 Schedule
Lecture 1:
• HIPAA Privacy Rule vs HIPAA Security Rule
• HITECH Act
Lecture 2:
• HIPAA -History
• Information Technology
• Breach Notification Rule
Lecture 3:
• Omnibus Rule
• Business Associates
Lecture 4:
• Current Court Cases (precedence)
• Paper Based PHI Concerns
• Disaster Recovery Concerns (Paper)
Day 2 Schedule
Lecture 1:
• Psych and Infectious Disease
• BYOD
• Texting and Emailing
Lecture 2:
• Choosing a HIPAA Consultant
• Choosing an IT Group
• Disaster Recovery Concerns (Electronic)
Lecture 3:
• Physical Setup
• Overseas Outsourcing
• What the Feds are Looking For (low hanging fruit)
Lecture 4:
• What are Factors That Can Get Your Practice Audited
• State Laws and Patient Ability to Sue
• How to Conduct a Risk Assessment
Speaker:
Brian L Tuttle
Sr Compliance Consultant & IT Manager, InGauge Healthcare Solutions
Brian L Tuttle, CPHIT, CHP, CHA, CBRA, CISSP, CCNA
Brian Tuttle is a Certified Professional in Health IT (CPHIT), Certified HIPAA Professional (CHP), Certified HIPAA Administrator (CHA), Certified Business Resilience Auditor (CBRA), Certified Information Systems Security Professional (CISSP) with over 17 years' experience in Health IT and Compliance Consulting.
With vast experience in health IT systems (i.e. practice management, EHR systems, imaging, transcription, medical messaging, etc.) as well as over 17 years' experience in standard Health IT with multiple certifications and hands-on knowledge, Brian serves as compliance consultant and has conducted onsite and remote risk assessments for over 1000 medical practices, hospitals, health departments, insurance plans, and business associates throughout the United States.
In addition, Mr Tuttle has served in multiple litigated court cases serving as an expert witness offering input related to best practices and requirements for securing and providing patient access to protected health information. Mr. Tuttle has also worked directly with the Office of Civil Rights (OCR) both in defending covered entities and business associates as well as being asked by the Federal government to audit covered entities and business associates on behalf of the OCR.
Almost all of Brian's clients are earned by referral with little or no advertising.
Brian is well known and highly regarded in medical circles throughout the United States for his quality work and down home southern charm
Mr Tuttle has a Master's Degree in Health Sciences from Georgia State University
Location: Washington, DC Date: February 8th & 9th, 2018 and Time: 9:00 AM to 6:00 PM
Venue: WILL BE ANNOUNCED SOON
Price:
Price: $1,295.00 (Seminar Fee for One Delegate)
Register now and save $200. (Early Bird)
Until January 10, Early Bird Price: $1,295.00 From January 11 to February 06, Regular Price: $1,495.00
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*
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At this seminar, world-renowned FDA Regulated Industry subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about FDA Regulated Industry and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to FDA Regulated Industry.
As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in FDA Regulatory -related industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants.
For More Information- https://www.globalcompliancepanel.com/control/spon...
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john.robinson-AT-globalcompliancepanel.com
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Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com
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Last modified: 2017-12-07 15:21:25