The Dark Report's Latest Audio Conference

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The Dark Report presents a brand-new audio conference...

How to Stay Legal in 2011: New Legal Issues and Regulatory Changes Affecting Clinical Laboratories and Pathology Groups

Tips and tactics for keeping your laboratory fully compliant
with new federal and state requirements



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YOUR PRESENTERS:

Richard Cooper, Attorney, McDonald Hopkins

Jane Pine Wood, Attorney, McDonald Hopkins

Justin M. Clark (Moderator), Director of Operations, THE DARK REPORT

Richard Cooper
Richard Cooper
Jane Pine Wood
Jane Pine Wood
Justin M. Clark of THE DARK REPORT
Justin M. Clark

___________________________________________________________________________

LIVE RECORDINGS AVAILABLE: Order Audio Now!

Lawmakers, regulators, and judges have been busy in 2010. New laws, amended regulatory requirements, and recent court decisions present clinical laboratories and anatomic pathology groups with new responsibilities-along with increased legal and compliance risk.

To help your laboratory stay "street legal" and fully compliant with these new regulations, you won't want to miss this DARK REPORT and DarkDaily.com annual legal/regulatory audio conference on Tuesday, October 19, 2010.

During the information-packed session you, your lab team and your attorney can all get concise information about the latest legal and regulatory developments-and find out what steps your laboratory can take to fulfill its responsibilities. Leading the discussion will be two of the nation's keenest legal minds in clinical laboratory and anatomic pathology issues: Jane Pine Wood and Richard Cooper of McDonald Hopkins.

New Legal Requirements and How They Could Impact Your Lab

Take self-reporting for starters. Are your lab's management and legal teams up-to-date on the new requirements for self-reporting? Self-reporting can be triggered by a host of issues, ranging from the discovery of Stark violations to errors affecting patient safety to overpayments made by federal and state payers. It even applies to overpayments from private Medicare Advantage health payers. So it's critical that your laboratory understands self-reporting obligations and has the right policies and procedures in place to guide your staff.

You'll also get the latest information on a brand-new legal/regulatory program known as the Medicare Recovery Audit Contractor program, or "RAC." Find out why Medicare now gives recovery audit contractors the power to conduct "medical necessity" audits at your hospital, health system or lab. RAC auditors can analyze claims with payment dates going back to October 1, 2007. The possible consequences are severe because every RAC audit has the potential to reveal Medicare fraud or abuse issues—possibly for your lab or pathology group! Our experts will alert you to key points that can help you avoid an audit—and its resulting problems.

Another change in federal law, effective in early 2010, was to the HIPAA disclosure rules. In the event of a breach of protected health information (PHI), labs and other providers are required to publicly disclose specific facts about the breach. This summer, the Boston Globe revealed that as many as 40,000 pathology reports and billing information from four local pathology groups had been found at a public dump.

Needless to say, this breach of PHI caught the four pathology groups and their parent hospitals by surprise. Find out how you can prepare your lab for these types of unexpected incidents involving PHI—as defined by federal laws—when you order to attend this very special event.

Get Answers From Two Clinical Lab and Pathology Experts

Legal experts Wood and Cooper will also address CLIA-the Clinical Laboratory Improvement Act. They'll help you understand what CLIA is looking for during lab inspections and how that's changing. You'll learn about the steps your laboratory should take when a deficiency is identified and "opened." Because serious deficiencies found during a CLIA inspection can result in sanctions against the pathologist who's on the license as the lab's medical director, this is information that pathologists can't afford to be without.

"How to Stay Legal in 2011: New Legal Issues and Regulatory Changes Affecting Clinical Laboratories and Pathology Groups" will introduce you to six brand-new or recent changes in laws, regulations, and market practices that govern how clinical labs and pathology groups conduct their affairs. Find out what you can do to ensure your lab stays on the right side of the law.

Register Today and Get Answers to Your Specific Questions!

And don't forget the question-and-answer session that allows you to pose your specific questions to these well-respected experts in laboratory medicine law and compliance. This direct access will help provide your team with the latest legal knowledge and precedents and get advice and insight tailored to the unique needs of your laboratory.

This learning session will help you better understand the steps your laboratory should take to comply with recent new laws and regulations. Best of all, our audio conference format allows you to assemble your senior executive team, compliance officers, and legal advisors to participate with you on the call. So don't wait! Order live digital recordings of this audio conference today!

THE DARK REPORT AUDIO CONFERENCE AT A GLANCE


COST: $245 Per 90 minute recording

TO ORDER RECORDINGS NOW:
Click here or call 1-800-560-6363 toll-free

For one low price—just $245—you and your entire team can take part in this fast-paced, insightful audio conference. Best of all you can here the questions asked to the panel at the end of the recorded session.

Here's just some of what you’ll learn during this in-depth 90-minute conference:

  • How to get your lab ready for "RAC": Why Medicare's Recovery Audit Contractor program may soon be at your hospital or laboratory.

  • Self-reporting surprises: The new regulations that require labs to report breaches of protected health information (PHI) as well as overpayments from Medicare, Medicaid, and Medicare Advantage.

  • Why your lab may be violating state law-in different states at the same time-and what you can do to fix the problem.

  • Tracking what new with CLIA lab inspections, plus insights into how to prepare your lab team for a clean inspection.

  • The latest on the new requirement that physicians sign lab test orders, plus the surprising news that most AP test requisitions don't comply with current law.

  • New HIPAA rules: How to prepare your lab to report privacy breaches to the right federal agency.

  • How your lab should respond when competing labs "give away" EMRs to doctors at no charge.

  • Conducting a compliance audit at your lab: Why it's your best insurance-but only if you follow these five essential steps.

  • EMR "donations" by labs to office-based physicians: The essential do's and don'ts.


    …plus much more!

How to Order:
1. Online
2. Call toll free: 800-560-6363.

Your audio conference audio order includes:

  • Downloadable PowerPoint presentations from our speakers
  • A full transcript emailed to you soon after the conference

    Order Now! Or for more information, call us toll-free at 800-560-6363.
Distinguished Presenters:

Richard CooperRichard Cooper, Esq. is Head of the National Healthcare Practice Group of McDonald Hopkins. He also serves on the firm’s Board of Directors. Mr. Cooper has a national health law practice that includes the representation of a large number of laboratories on corporate, regulatory/compliance, contracting, strategic, venture and M&A/joint venture matters. Laboratory clients include both independent and hospital-owned laboratories plus clinical, anatomic and specialty labs. He has been involved in a substantial number of lab M&A/joint venture transactions and frequently counsels clients on strategic planning issues related to preparing labs for sale. He received his JD from Georgetown University.

 


Jane Pine WoodJane Pine Wood is a member of McDonald Hopkins, LLC which specializes in health law, including regulatory, compliance, and contractual matters, including Medicaid and Medicare reimbursement issues. Ms. Wood represents physicians, hospitals, clinical and anatomic laboratories, imaging centers, home health agencies, mental health providers, clinics, independent practice associations and integrated delivery systems in corporate, regulatory, reimbursement, contractual and other areas. She received her J.D. degree in 1987 from Vanderbilt University School of Law and is admitted to practice in Massachusetts, Ohio and Tennessee.

 

 



Yes, i want to register Now!

 

ACCENT® Continuing Education Credit
The American Association of Clinical Chemistry (AACC) designates this program for a maximum of 1.5 ACCENT® credit hours towards the AACC Clinical Chemist’s Recognition Award. AACC is an approved provider of continuing education for clinical laboratory scientists in the states of California, Florida, Louisiana, Montana, Nevada, North Dakota, Rhode Island, and West Virginia.

 

 

 

 

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