EY
Fraud Investigation & Dispute Services, Life Sciences team

Tighter competition, regulatory scrutiny and tough enforcement heighten the risk of litigation and non-compliance. In your industry, compliance issues and risk factors need to be addressed at every turn from research and development to marketing strategies and supply chain integrity. And the scrutiny of regulators and customers alike is increasing and rapidly changing.

Our professionals understand the complex issues facing pharmaceutical, biotechnology and medical device companies. We have significant experience helping companies evaluate and manage those aspects of their businesses that pose the greatest potential risks. Our dedicated team includes CPAs, government contract analysts, economists, licensed pharmacists and certified fraud examiners, as well as former pharmaceutical executives, ethics and compliance officers and government auditors, investigators and prosecutors.

For more information visit www.ey.com or contact: Ted Acosta, Principal, Fraud Investigation & Dispute Services (212) 773-3022 or Mariusz Witalis, Partner, Fraud Investigation & Dispute Services +48 22 557 7950.

Global Pharmaceuticals and Life Sciences Industry Group at PwC
The Global Pharmaceuticals and Life Sciences Industry Group at PwC is dedicated to delivering effective solutions to the complex business challenges facing pharmaceutical and life sciences companies. A global leader in serving the pharmaceutical and life sciences industry, PwC has extensive experience working with companies on industry-specific strategic, operational, and financial issues. Our capabilities include assurance, tax and advisory services, as well as industry specialised services in regulatory compliance, risk management, and transaction support. In helping our clients, we draw on the full knowledge and skills of PwC's professionals. More than 184,000 people in 157 countries connect their thinking, experience and solutions to build public trust and enhance value for clients and their stakeholders. www.pwc.com/pharma

Cegedim Relationship Management
Cegedim Relationship Management is the Life Sciences industry's leading global provider of Customer Relationship Management (CRM) and Regulatory Compliance solutions. Cegedim Relationship Management's industry leading aggregate spend solution, AggregateSpend360, helps pharmaceutical and medical device companies efficiently comply with local, regional and global transparency requirements -- such as the Sunshine Act in the US, the Réforme du Médicament in France, disclosure guided by the European Federation of Pharmaceutical Industries and Associations (EFPIA), and anti-bribery regulations such as the UK Bribery Act and Foreign Corrupt Practices Act.

AggregateSpend360 is a pro-active, web-based application that automates and streamlines the tracking and reporting of all expenditures between Life Sciences companies and healthcare professionals. With a flexible business rules engine that transforms, aggregates, and reports data and features that include prebuilt reporting templates and automated report due-date reminders, AggregateSpend360 allows you to align compliance standards across the enterprise and across geographies without overburdening internal resources. The process can be leveraged by accurate customer data management and the integration of a wide range of enterprise applications -- CRM, ERP, Finance, Travel & Expense and HR -- for in-depth analysis and improved business insights.

For more information visit www.cegedim.com/aggregatespend or call (888) 336-3748.

AHM
AHM is a leading global provider of technology and service solutions to manage compliant interactions with healthcare professionals for the highly regulated life sciences industry. For more information visit www.ahmdirect.com.

AlixPartners, LLP
AlixPartners, LLP is a global business-advisory firm offering comprehensive services in four major areas: enterprise improvement, turnaround and restructuring, financial-advisory services and information-management services. We serve life sciences companies with respect to a wide range of complex issues in matters involving litigation, compliance, corporate investigations, economic consulting, valuation, due diligence and transactions. In addition, we provide litigation consulting to companies and their counsel in high-stakes situations involving various types of allegations. Our professionals have testified as expert witnesses and advised companies and their counsel in matters involving the False-Claims Act, the Hatch-Waxman Act, and those involving breach of contract, intellectual property, product liability and antitrust. We specialize in urgent, high-impact situations when results really matter and have more than 1200 professionals in 19 offices across North America, Europe, and Asia. For more information visit: AlixPartners' Life Science Services or contact Yogesh Bahl, Managing Director, 212.845.4082.

Arnold & Porter
Arnold & Porter LLP, an 800 lawyer firm with offices in the US and Europe, is ideally positioned to serve the needs of the Biopharmaceutical and Medical Device community. Our team of more than 50 regulatory and compliance attorneys advise life sciences companies in developing, implementing and refining global compliance programs that address regulatory and enforcement risks confronted at each stage of product research and development, manufacturing, marketing and distribution. We regularly advise companies in matters raising complex compliance issues, developing practical solutions to the challenges associated with conducting clinical trials in jurisdictions with varying healthcare systems, the complexities and risks of pharmaceutical supply chains, interactions with physician and patient populations, managing co-development and co-promotion arrangements, and outsourcing of functions in areas such as research, pharmacovigilance and manufacturing. We also vigorously defend our clients in a broad range of investigations and enforcement matters.

For more information please visit www.arnoldporter.com or contact Daniel A. Kracov, Partner, (202) 942-5120.

Baker & McKenzie
Baker & McKenzie's involvement in the pharmaceutical, healthcare and medical industry stretches over 50 years. Our global team of more than 450 lawyers with deep experience in local regulatory processes and laws affecting pharmaceutical, medical device and biotechnology businesses, helps healthcare companies stay ahead in established markets and gain ground in new ones.

Baker & McKenzie has a legal network spanning 74 locations in 46 countries. We provide a wide range of compliance advice and assistance, including in relation to: anticorruption, trade sanctions and export controls, customs, antitrust, data protection, environmental, healthcare marketing and promotional law, and strategic advice in government enforcement proceedings. In the area of global compliance, we provide integrated counsel to ensure consistency across borders and markets.

For more information, please visit www.bakermckenzie.com, or contact Jane Hobson, Chair Global and EMEA Pharmaceuticals & Healthcare Industry Groups, +44 20 7919 1907.

Clifford Chance
International law firm Clifford Chance combines the highest global standards with local expertise. Leading lawyers from different backgrounds and nationalities come together as one firm, offering unrivalled depth of legal resources across the key markets of the Americas, Asia Pacific, Europe and the Middle East.

Established in the early 1990s, Clifford Chance's Global Healthcare and Life Sciences team consists of more than 100 dedicated lawyers in 36 key centres worldwide. Having cultivated an expertise in the industry over nearly two decades and worked with many of the world's leading pharmaceutical, biotechnology, medical device and health care services companies, we understand the importance of anticipating regulatory and contractual issues in the context of corporate investment, finance, strategy and operations. We have close relations with a number of multi-nationals as well as national and international trade associations in the pharmaceutical and medical device industries.

Clifford Chance has 36 offices in 26 countries and over 3400 legal advisors globally.

For more information, please visit www.CliffordChance.com or contact Peter Dieners, Partner, Germany, +49 211 4355 5468.

Davis Wright Tremaine
Those of us in the Davis Wright Tremaine health care practice group devote nearly all of our time to industry-specific matters. This allows us to develop niche practices within the field that serve needs unique to the health care market. We also understand the business issues and regulatory developments that affect health care delivery and compliance, and as a unified team we can match the attorney with the niche expertise that best addresses client needs. For more information visit our website at www.DWT.com.

Hogan Lovells
Hogan Lovells provides high quality advice to corporations, financial institutions, and governmental entities across the full spectrum of their critical business and legal issues globally and locally. Bringing together the combined strengths of our predecessor firms, we have more than 2,300 lawyers operating out of more than 40 offices in the United States, Latin America, Europe, the Middle East, and Asia. With more than 100 lawyers serving the pharmaceutical and biotechnology sectors, including many with experience at the FDA, CMS and other key agencies and in industry, and others holding advanced degrees in relevant disciplines, we offer timely, effective counsel on matters that include product development, approval and post-approval compliance, and the development of next-generation products. High rankings in Chambers, Legal 500, and other global directories speak to the quality and impact of our services.

Whether your products are traditional drugs or biotechnology products, we work with you to successfully develop and commercialize products, addressing issues of regulatory approvals and compliance; coverage, reimbursement, and pricing; and careful use of intellectual property and regulatory exclusivities to manage product life cycles. Our multidisciplinary team leverages the skills and experience of colleagues in other disciplines - including healthcare compliance (such as coverage, reimbursement, pricing, and fraud and abuse prevention), public policy, intellectual property, corporate and securities law, and litigation - to provide integrated, strategic, and practical advice for successful product development and marketing and effective responses to regulators and competitors.

For more information, visit www.hoganlovells.com or contact Marketing Manager Tara Busby at (202) 637-6912.

King & Spalding
Celebrating more than 125 years of service, King & Spalding is an international law firm that represents a broad array of clients, including half of the Fortune Global 100, with 800 lawyers in 17 offices in the United States, Europe, the Middle East and Asia. The firm has handled matters in over 160 countries on six continents and is consistently recognized for the results it obtains, for uncompromising commitment to quality and for dedication to understanding the business and culture of its clients. In 2013, King & Spalding was chosen by U.S. News & World Report and Best Lawyers as the "Law Firm of the Year" for FDA law and ten King & Spalding lawyers were identified as 'life sciences stars' in the 2013 edition of LMG Life Sciences.

For more information about our FDA & Life Sciences practice, please contact Mark Brown at (202) 626-5443.

Polaris Solutions, BV
Polaris Solutions, BV is the leading management consulting and technology provider of innovative, high quality, end-to-end compliance solutions for life sciences companies. We provide the best and brightest talent, the best industry platforms and best practices to improve clients' businesses, on-time, on-budget and on-scope, to achieve the highest level of customer satisfaction in the industry.

For more information visit www.polarismanagement.com or contact our Amsterdam office at +31.20.240.2518.

Porzio Life Sciences, LLC
Porzio Life Sciences, LLC (PorzioLS) provides the life science industry with Internet-based products enabling companies to comply with marketing and sales federal and state laws and regulations, as well as, distribution licensing, sampling and a growing body of state life science compliance requirements. PorzioLS provides compliance tools and customized services, related to the PDMA, anti-kickback statutes, aggregate spend reporting, OIG and CMS guidances, OPDP promotional violations, False Claims Act and FDA regulations, such as the Porzio Compliance Digest and Porzio AggregateSpendID, a best in class aggregate spend system capable of handling state and federal transparency reporting and dispute resolutions, in addition to sample transparency reporting.

Porzio AggregateSpendID streamlines state and federal marketing disclosures by automating the collection and accurate reporting of expenses directed to healthcare practitioners and organizations. The searchable databases of the Porzio Compliance Digest cover drug and device distribution licensing, transparency legislation, sample and trade product distribution, and trends in government investigations.

Through our Distribution Licensing Services, we identify and attain all required licenses based on a company's unique distribution model. Finally, our formula-based approach to sample accountability, Significant Loss Threshold Assurance, ensures that customers neither over or under report sample losses. These compliance tools and customized services facilitate companies' compliance with federal and state marketing and sales regulations, which has propelled PorzioLS into an industry leader in life science marketing and sales compliance.

The International Life Sciences Transparency Database provides guidance on non-US disclosure requirements pertaining to interactions with HCPs and HCOs and provides easy-to-read excerpts and summaries (in English) on crucial global information including, non-US reporting requirements concerning HCP/HCO transfers of value, anti-bribery and anti-corruption, prohibitions and financial limitations on HCP/HCO interactions and data privacy. The International Database also contains EFPIA, Eucomed, IFPMA and Mecomed international industry and member association codes.

Strengthen your compliance program today by visiting www.porziolifesciences.com or contacting us 877-477-7411.

Sidley Austin
Sidley Austin LLP is a premier law firms with an internationally recognized life sciences practice, representing large to start-ups pharmaceutical, biotechnology, medical device, dietary supplements and food clients. Many lawyers in our team are acknowledged leaders in regulatory, compliance and enforcement. Sidley consistently ranks among the top firms in Asia, Europe and the U.S., and recently was named "Life Cycle: Firm of the Year" by LMG Life Sciences Awards 2013. We also received first-tier national rankings in Biotechnology Law, FDA Law and Healthcare Law in the U.S. News -- Best Lawyers "Best Law Firms" rankings for the fourth consecutive year, and each year since the survey's inception. Sidley is also recognized for service and responsiveness, having been once named the "Most Recommended Law Firm in the Pharmaceutical Industry" in the BTI Industry Power Rankings. For more information visit www.Sidley.com or contact Scott Bass, (202)736-8684 and James Stansel, (202) 736-8092.

Skadden, Arps, Slate, Meagher & Flom LLP
With approximately 1,800 attorneys in 22 offices on five continents, Skadden represents a broad range of clients in all sectors of the health care industry. Skadden represents pharmaceutical and medical technology clients at every stage of a company's development, from initial public offering to global M&A and corporate finance, and all manner of litigation and regulatory matters, including government investigations, mass torts and product liability litigation, intellectual property counseling and patent litigation, and FDA and healthcare compliance. Skadden has assisted many companies in developing and implementing global anti-bribery and anti-corruption compliance programs, and represented numerous companies in related government investigations.

Seton Hall Law School
Seton Hall Law's Center for Health & Pharmaceutical Law & Policy advances scholarship and recommendations for policy on the varied and complex issues posed by health and pharmaceutical law. As a nationally ranked Health Law program, the Center fosters informed dialogue between policymakers, consumer advocates, the medical profession, and industry in the search for solutions to the ethical, legal and social questions presented in the health and pharmaceutical arena.

In addition, the Center is a leader in providing healthcare compliance education and training in the U.S., and Europe and Asia-Pacific on national and international mandates that apply to the safety and promotion of drugs and devices. The Center also hosts conferences and educational programs, inviting leading experts from the public and private sectors to examine cutting edge policy issues.

Launched in April 2007, the Center extends Seton Hall Law School's national reputation in health law to the life sciences arena and offers a challenging health law curriculum through its M.S.J., J.D. and LL.M. degree programs, and online Graduate Certificates, and online M.S.J. The Center operates under the leadership of a full-time Executive Director, Simone Handler-Hutchinson, and draws upon the intellectual strength of the Seton Hall Law School faculty and research fellows who bring to the Center's work nationally recognized expertise in health and pharmaceutical law, not-for-profit governance, intellectual property law and bioethics, among other areas.

For further information or inquiries about the Center and its varied programs, please visit the website at law.shu.edu/CenterforHealth and law.shu.edu/compliance, or contact Simone Handler-Hutchinson, Executive Director of the Center.