Webcast - Pharmaceutical/Biotech Accounting & Reporting Update Conference 2012

Get updates on changing regulations and the latest best accounting practices for pharmaceutical and biotech companies

Webcast - Pharmaceutical/Biotech Accounting & Reporting Update Conference 2012

CPE Credit: 8 Hours

Price: $499.00

NASBA Field of Study: Accounting

$499 per day or take both days for just $899!

Overview

Get the most recent updates on changing regulations, industry trends and the latest life sciences accounting and reporting best practices. Discover how health care reform, the credit crisis, the SEC and international tax planning will impact the financial reporting of pharmaceutical and biotech companies. Plus, gain technical guidance from top level pharmaceutical finance officers and government regulators in this highly focused two-day webcast.

This two-day webcast is comprised of two 8-hour sessions. Take both days for just $899!
 

DAY ONE HIGHLIGHTS


•  The current environment and key emerging
   trends

•  Health care reform update

•  Regulatory update: aggregate spend reporting
   and the Sunshine Act

•  Accounting for debt financing and equity
   transactions

•  Valuation considerations

DAY TWO HIGHLIGHTS


•  FASB and technical accounting update

•  Revenue recognition and leases

•  Deal-making in the industry

•  M&A activity: current trends and expectations
   in the industry

•  Projecting pharmaceutical business trends

•  SEC comment letters

•  Leadership in pharmaceuticals and
   biotechnology

 

This is a live broadcast of our
Pharmaceutical/Biotech Accounting & Reporting Update Conference 2012

Agenda

MAY 16, 2012


Chairman’s Welcome & Opening Remarks
8:45 – 9:00 AM

The Current Environment & Key Emerging Trends
9:00 – 10:15 AM

Growth market and emerging opportunities
Market and health care trends
Scientific and technological trends
In-house discovery vs. in-licensing and strategic alliances

Break
10:15 – 10:30 AM

Health Care Reform Update
10:30 AM – 12:00 PM

New proposed rules for AMP and BP and the overall impact to the Medicaid Drug Program
Potential impact on AMP calculation methodology and Medicaid rebate liabilities
Emerging industry best practices to address the proposed rules
Preparations that will be necessary to comply with proposed new rules
Best practices for compliance
Systems and procedural requirements
Documentation and testing practices

Luncheon
12:00 – 12:45 PM

Regulatory Update: Aggregate Spend Reporting & the Sunshine Act
12:45 – 2:00 PM

Update/status of the proposed changes to the Sunshine Act
Issues within the Spend Reporting Compliance Continuum
Aggregate spend disputes and inquiries from health care professionals

Break
2:00 – 2:15 PM

Valuation Considerations
2:15 – 3:45 PM

M&A and intangible asset valuations
Changes to the AICPA practice aid for IPR&D
Alternative methodologies for IPR&D valuation
Discount rate considerations
Inventory valuation and complexities in the pharmaceutical industry
Contingent consideration: accounting treatment and royalty arrangements
Day Two impairment considerations and “Step 0”

Break
3:45 – 4:00 PM

Accounting for Debt Financing & Equity Transactions
4:00 – 5:00 PM

In-depth analysis of accounting issues
Equity derivatives
Convertible securities
Accounting for debt modifications

Cocktail Reception
5:00 – 6:00 P
M

 

MAY 17, 2012


FASB & Technical Accounting Update: Roundtable Brief (Part I)
8:30 – 10:00 AM

Revenue recognition and leases
Collaborations, joint ventures and other alliances
Current rules and new developments

Break
10:00 – 10:15 AM

FASB & Technical Accounting Update: Roundtable Brief (Part II)
10:15 AM – 12:00 PM

Non-GAAP measures
Loss contingencies
Income taxes, including repatriation of earnings
Impairments

Luncheon
12:00 – 1:00 PM

Deal-Making in the Industry
1:00 – 2:15 PM

M&A activity: current trends and expectations in the industry
M&A best practices
   – Initial interest and due diligence
   – Contract support
   – Closing and integration

Key diligence areas of focus and value drivers: US vs. ex-US emerging markets

Break
2:15 – 2:30
PM

SEC Comment Letters
2:30 – 3:45 PM

Key SEC staff messages
Current issues impacting pharmaceutical companies
Past areas of SEC staff focus
Potential outcomes of a comment letter
How does a review result in enforcement investigation?
Best practices footnote disclosures
Responding to the staff

Break
3:45 – 4:00 PM

Leadership in Pharmaceuticals & Biotechnology: Executive Roundtable
4:00 – 5:00 PM

Life cycle management issues
The impact of health care reform on the pharmaceutical and biotechnology industries
Drug portfolio diversification
Exclusivity losses
Projecting pharmaceutical business trends in highly competitive markets

Conference Ends
5:00 P
M

 

Location

Eastern Time
Live Webcast from
Iselin
NJ

Speakers

SPEAKERS INCLUDE


Ben Barrameda, Partner, Cumulus Consulting LLC

Glenn Hunzinger, Transactions Services Director, PwC

David Levi, Director of Technical Accounting, Bristol-Myers Squibb

Mark Linver, Managing Director, Huron Life Sciences

Debbie Paul, Senior Vice President North America, EvaluatePharma USA, Inc.

John Pennett, Partner-in-Charge, Life Sciences Group, EisnerAmper

Reuven Pinsky, Director, Transaction Services, PwC

Jeffrey Schaeffer, Senior Manager, National Professional Practice, Ernst & Young LLP

Jay Seliber, Assurance Partner, PwC

Donald Walker, Senior Managing Director, FTI Consulting

Kristina Winch, USP Technical Accounting and Controls Manager, Bristol-Myers Squibb

…and more!

Workshop

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Forum

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