Why you Should be Worried about HIPAA 2017


This seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits or (even worse) litigation occurs against your organization under state laws of negligence.
It will also address major changes under the Omnibus Rule and any other applicable updates for 2017. Areas covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to IT.
The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, there is so much misleading information all over regarding the do's and don'ts with HIPAA - I want to add clarity for compliance officers
I will uncover myths versus reality as it relates to this very enigmatic law based on over 1000 risk assessments performed as well as years of experience in dealing directly with the Office of Civil Rights HIPAA auditors.
I will also speak to real life audits conducted by the Federal government (I've been on both sides of these audits) what your highest risks are for being fined (some of the risk factors may surprise you).
In addition, this course will cover the highest risk factors for being sued for wrongful disclosures of PHI and the manner in which patients are now using state laws to sue for wrongful disclosures.
Don't always believe what you read online about HIPAA, especially as it relates to encryption and IT, there are a lot of groups selling more than is necessarily required.

Why you should attend:

There are major changes to HIPAA set forth by the Federal government whereby patients can receive remedies for HIPAA violations and business associates (i.e. law firms) must now comply directly with HIPAA.
Omnibus has changed the HIPAA landscape for good!
State laws are now in place increasing liability for patient remedies!
This once rarely enforced law has changed and you need to know what's going on!
Protect your practice or business!
Why are the Feds enforcing after all these years?
We will be discussing some of the changes taking place in Washington with the Health and Human Services in regards to the enforcement of the HIPAA laws already on the books.
I will also thoroughly go through multiple litigated cases I have been a part of involving patients suing for HIPAA violations - THIS IS A MUST TO UNDERSTAND!!
Changes affecting law firms dealing with protected health information
I will also be discussing factors might cause an unwanted visit or letter from the Office of Civil Rights and how to prepare for the audit and deal with the Feds.

Areas Covered in the Session:

•	History of HIPAA
•	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
•	Business Continuity/Disaster Recovery Planning
•	Business Associates and HIPAA
•	In depth discussions on IT down to the nuts and bolts
•	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.


Day 1 Schedule
Lecture 1: HIPAA -History
Lecture 2: HIPAA Privacy Rule vs HIPAA Security Rule
Lecture 3: HITECH Act
Lecture 4: Information Technology
Lecture 5: Breach Notification Rule
Lecture 6: Omnibus Rule
Lecture 7:Business Associates
Lecture 8: Current Court Cases (precedence)
Lecture 9: Paper Based PHI Concerns
Lecture 10: Disaster Recovery Concerns (Paper)
Lecture 11: Psych and Infectious Disease

Day 2 Schedule

Lecture 1: Choosing a HIPAA Consultant
Lecture 2: Choosing an IT Group
Lecture 3: Disaster Recovery Concerns (Electronic)
Lecture 4: Physical Setup
Lecture 5: Overseas Outsourcing
Lecture 6: BYOD
Lecture 7: Texting and Emailing
Lecture 8: What the Feds are Looking For (low hanging fruit)
Lecture 9: What are Factors That Can Get Your Practice Audited
Lecture 10: State Laws and Patient Ability to Sue
Lecture 11: How to Conduct a Risk Assessment
Lecture 12: How to Write Policies and Procedures

Location:  SFO, CA Date:  September 7th & 8th, 2017 and Time: 9:00 AM to 6:00 PM
Venue:  Hilton San Francisco Airport Bayfront   600 Airport Blvd, Burlingame, CA 94010

Register now and save $200. (Early Bird)
Price: $1,295.00 (Seminar Fee for One Delegate)
Until July 31, Early Bird Price: $1,295.00 From August 01 to September 05, Regular Price: $1,495.00
Register for 5 attendees   Price: $3,885.00      $6,475.00 You Save: $2,590.00 (40%)*

Sponsorship Program benefits for “Quality Assurance Auditing for FDA Regulated Industry” seminar
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/sponsorship  
Contact us today!

NetZealous LLC DBA GlobalCompliancePanel
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
 Website: http://www.globalcompliancepanel.com

Registration Link - http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901046SEMINAR?biotechsciencenews-September-2017-SEO

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Schedule of Presentations:

Thursday, September 7, 2017
Friday, September 8, 2017
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