AIS Audioconferences - Reconciling Part D Enrollment Data: Strategies to Avoid Becoming an Enforcement Target; Wall Street’s 2009 Outlook for Health Plans: Prognosis for the Industry and Individual Plans


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Visit AISEducation.com for more news and strategic information for today's business leaders
 
Audioconference: Wednesday, December 17, 2008
The Obama Administration’s Pharmaceutical Initiatives: Likely Impact on Cost, Utilization and Management
AIS E_Savings Club

The spotlight is on pharmaceutical costs as the Obama administration and new Congress set their sights on major changes to the U.S. health care system. Direct negotiation of Medicare Part D drug prices, reimportation of pharmaceuticals and authorization for generic biologics all have wide support among incoming policymakers. And past experience shows that commercial payers tend to follow the federal government’s lead on these issues. Find out what changes to the pharma regulatory landscape are likely during the upcoming Obama administration, and how they will impact your future strategies and bottom line.

 
Wednesday, December 17, 2008
1:00 - 2:30 Eastern time
12:00 - 1:30 Central time
11:00 - 12:30 Mountain time
10:00 - 11:30 Pacific time
Sponsored by Atlantic Information Services, Inc., publisher of Specialty Pharmacy News, Drug Benefit News and Health Plan Week.

Speakers
Designed For

How the Audioconference Works

Shipping Information

Written Materials

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Print an order form:
If you do not wish to place your order online, click here to download a printable order form (PDF file), then submit your order via fax or mail, as directed on the form.

 

 
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All formats come with written materials*
Join us on December 17!
Order Now Audioconference ($329)
Just $299 (Save $30!)
Pub code: C8P33-ENLAD
Order Now Audioconference and CD ($421)
Just $391 (Save $30!)
Pub code: C8P33 & C8P33T-ENLAD
Order Now Audioconference and MP3 file ($421)
Just $391 (Save $30!)
Pub code: C8P33 & C8P33F-ENLAD
Can't make it on December 17?
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CD ($329) Just $299 (Save $30!)
Pub code: C8P33T
-ENLAD

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MP3 file ($329) Just $299 (Save $30!)
Pub code: C8P33F
-ENLAD


* A copyright release in the Printed Materials will permit you to make photocopies for each person listening to the Audioconference and/or the recording.

With a popular new president and a Democratic-controlled Congress preparing to assume power next month, major changes in pharmaceutical regulation and legislation are highly likely. With the prospect of sudden, dynamic change, unprecedented new challenges and opportunities could soon exist for your organization.

Join us on Dec. 17 and hear two leading pharmaceutical industry analysts assess the chances of dramatic impact on all links in the drug chain, from manufacturers, PBMs and specialty pharmacies to health plans, physicians and patients. You’ll get insider perspectives on questions such as:

  • Will Medicare be able — and willing — to directly negotiate with manufacturers on prices for Part D drugs? How would this impact private plans?
  • Were Medicare able to directly negotiate with manufacturers, would it have the ability to exclude drugs from its formulary when manufacturers refuse to play ball?
  • Will the reimportation of drugs from Canada and other countries be permitted? If so, what would be the ramifications…and for whom?
  • How is coverage of therapies likely to change, including fail-first policies, clinical-data effectiveness, compendia used and least-costly alternatives?
  • What are the chances of legislation that creates an approval pathway for follow-on biologics? How would it address data exclusivity, patent protection and other complex issues?
  • Will Part D coverage of home infusion drugs be extended to also cover the administration and supplies required?
  • Which potential reimbursement changes could impact the market, including rate changes in hospitals and physician offices and the postponement of the Medicare Part B Competitive Acquisition Program?

Team-Wide Training at Its Best (and most cost- and time-efficient). Gather your management team around the table on December 17 for one low single-participant price. And photocopy for each of them as many copies of our printed materials as you need. Managers throughout your organization will learn about major changes ahead that could impact the pharmaceutical regulatory landscape.

 

Speakers

MARC SAMUELS, J.D., is a partner with Washington, D.C.-based HillCo Partners, a strategic advisory firm focused on providing timely, strategic advice about reimbursement policy risks and opportunities presented in the current public and private health care environment. He provides support to product management and corporate reimbursement and policy resources beginning when a product is in Phase II clinical research through the product life cycle to patent expiration. Much of his time is spent educating and advising clients planning significant new initiatives in the regulatory arena, and providing independent expert opinion on policy and business issues in health care, helping to explore the ramifications of various public and reimbursement policy options. Mr. Samuels also works with the investment community to identify potentially material changes in the regulatory and reimbursement environments faced by health care companies and to assess problems and opportunities in potential health care investments before the beginning of active due diligence. He and his partners have each played pivotal roles in developing policy and affecting the regulatory agenda on some of the most critical coverage and payment policy issues affected by Medicare and Medicaid, including age-related macular degeneration, left ventricular assist devices, radiopharmaceuticals, obesity as an illness, anti-cancer therapies, intravenous immunoglobulin, home infusion, average sales price and average manufacturer price reform, and coverage of vaccines, oral antiemetics, and vitamin-enhanced products under Medicare Part D. Mr. Samuels attended the University of Texas School of Law, Yale School of Medicine and the University of Michigan. He is a board member of the University of Houston Health Law & Policy Institute.

BONNIE WASHINGTON is a vice president with Avalere Health LLC.  She provides clients with strategic policy advice on a wide range of issues including Medicare policy development, health reform and commercial strategy. Ms. Washington has particular expertise in the Medicare prescription drug benefit, Medicare Advantage, and pharmaceutical and health plan issues. Prior to joining Avalere, she led health policy development efforts for Novartis Pharmaceuticals Corp. and Ovations, a UnitedHealth Group company. Before her industry experience, Ms. Washington led the Office of Legislation at CMS. Specifically, she advised and represented the CMS administrator on legislation and policy related to Medicare, Medicaid and the State Children’s Health Insurance Program (SCHIP). She also represented the administration before members of Congress and congressional staff. Previously, Ms. Washington served as an analyst with the Office of Management and Budget, advising OMB and White House policy officials on Medicaid and SCHIP policy options. She holds a B.A. from Loyola College in Maryland and an M.Sc. from the London School of Economics.

Moderator: Angela Maas, managing editor of AIS’s Specialty Pharmacy News.

A concluding 30-minute Q&A session will give you a chance to get expert feedback on major changes ahead under President Obama that could impact the pharmaceutical regulatory landscape.

 

Designed Especially For

Government affairs and compliance directors; strategic planners; product development, contracting and marketing executives; pharmacy, clinical services and medical directors; and financial and operations executives at

  • Health plans
  • Specialty pharmacies
  • PBMs and pharmacy benefit administrators
  • Pharmaceutical manufacturers
  • Infusion suites
  • Employers
  • Group-purchasing organizations
  • Physician groups
  • Consulting firms
  • Disease management companies
  • Third-party administrators

 

How the Audioconference Works

1. Register above (or call 800-521-4323 to register).

2. When you register, you will receive a confirmation by e-mail from AISconferences@aispub.com, with a toll-free number and password that will connect you to the Audioconference on Wednesday, December 17, 2008 (1 p.m. Eastern time). There is no limit on the number of participants from your office, but the registration fee covers only one phone dial-in. Additional dial-ins require additional registration fees. For discount pricing on additional phone lines, please contact customer service at 800-521-4323.

3. You will also receive copies of the Printed Materials (in PDF format by e-mail).

4. Listen in to the Audioconference as you follow along with your Printed Materials.

5. The final segment of the Audioconference will let you ask questions and get answers about major changes ahead under President Obama that could impact the pharmaceutical regulatory landscape.

6. Cancellation Policy: To cancel your registration for this event and receive a full refund, you must contact customer service at 800-521-4323 no later than 48 hours prior to the scheduled start of the audioconference. Any cancellations received after dial in information and supplemental materials have been sent (48 hours prior to the start of the audioconference) will receive a CD of the audioconference or a credit valid for one year. Your credit (the cost of the audioconference) will be applied toward the purchase of any AIS product or audioconference.

Can't make it on December 17? Order the CD or MP3 file and Printed Materials.

Remember: A copyright release in the Printed Materials will permit you to make photocopies for each person listening to the Audioconference and/or recording.

This Audioconference limits your time, expense and inconvenience. There is no need to leave your office or incur travel expenses to find out about major changes ahead under President Obama that could impact the pharmaceutical regulatory landscape. And your entire team will benefit at the same low single-participant price. For more information, or to register, call 800-521-4323 or click above.

 

Shipping Information

Please note that CDs and MP3 files will be available within three weeks of the conference date.

Audio CDs (and accompanying written materials) are shipped via UPS. Please give us your street address when you order (UPS does not deliver to PO boxes). You should receive your order within 5-7 business days.* Shipping cost is $5.

MP3 files will be delivered as a download link within a PDF file of the accompanying written materials. Shipping will NOT be charged for this item.

If you order the MP3 file before the conference date (by itself or in combination with the live audioconference), you will be sent an e-mail with the PDF file attached once the file is available.*

After the MP3 file is available*, if you order the MP3 file on this Web site through our secure shopping cart, a link will appear directing you to download the PDF file. This link will be accessible only for 24 hours, so be sure to save the file to your computer. If you order through our customer service department (by phone, mail, fax or e-mail), you will be sent an e-mail with the PDF file attached.

Rush Orders: Please call us at 800-521-4323 to place a rush order.* We will overnight your order for an additional charge of $30, or you can give us your FedEx or UPS account number and we will charge the shipping to your account. Rush orders placed after 3:00pm EST will not be shipped out until the next business day.

*CDs and MP3 files will be available within three weeks of the conference date.

 

Written Materials

Listeners will also receive practical written information to supplement information covered by the audioconference speakers.

 

For further information call 800-521-4323 or e-mail customerserv@aispub.com

 


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