pharmaceutical compliance congress
pharmaceutical compliance congress
pharmaceutical compliance congress
pharmaceutical compliance congress
pharmaceutical compliance congress
pharmaceutical compliance congress

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We thank the following Grantors and Exhibitors for their support in helping to make this conference possible.


PwC's Pharmaceutical and Life Sciences Industry Group is dedicated to delivering effective solutions to the complex regulatory, strategic and operational challenges facing pharmaceutical, biotechnology and medical device companies. We provide industry-focused assurance, tax and advisory services to build public trust and enhance value for our clients and their stakeholders. More than 180,000 people in 158 countries across our global network of firms share their thinking, experience and solutions to develop fresh perspectives and practical advice. For more information visit and


You can't predict the future, but you can prepare for a changing market and heightened regulatory landscape. At Deloitte, we help our clients develop strategies, mitigate risks, and prepare for the future of health care. With over 70 years of industry experience and the innovation, deep understanding, and commitment of over 3,000 professionals, we provide a range of technical and advisory services to help clients transform their organizations. Our approach can deliver strategies that take the shape of your business goals, today and into tomorrow. To learn more, visit


Cegedim Relationship Management
Cegedim Relationship Management is a technology information services company delivering innovation to help transform commercial and compliance operations in U.S. healthcare. Its first-to-market and industry leading AggregateSpend360™ solution helps pharmaceutical and medical device companies across the globe comply with various transparency and disclosure regulations, including the U.S. Patient Protection and Affordable Care Act (frequently referred to as the Sunshine Act).

AggregateSpend360 is a proactive, web-based application that automates and streamlines the tracking and reporting of all expenditures between Life Sciences companies and healthcare. Integration with Cegedim's optional data services and a wide range of enterprise applications (CRM, ERP, Finance, Travel & Expense and HR) helps to ensure accurate reporting and provides in-depth analysis and improved insight on HCP expenditures. For more information visit, or call 888-336-3748.

EY's Fraud Investigation & Dispute Services
Dealing with complex issues of fraud, regulatory compliance and business disputes can detract from efforts to succeed. Better management of fraud risk and compliance exposure is a critical business priority -- no matter the industry sector. With our more than 2,000 fraud investigation and dispute professionals around the world, we assemble the right multidisciplinary and culturally aligned team to work with you and your legal advisors. And we work to give you the benefit of our broad sector experience, our deep subject matter knowledge and the latest insights from our work worldwide.

For more information visit or contact Ted Acosta, Principal, Fraud Investigation & Dispute Services, Life Sciences Leader, (212) 773-3022.

Huron Life Sciences
Pharmaceutical, medical device, and biotechnology companies face a highly competitive marketplace and increasing regulatory and government scrutiny. Huron's Life Sciences practice provides the regulatory, operational, financial, and strategic expertise needed to meet these challenges, enabling companies to optimize performance while mitigating compliance risk.

  • Transparency and Disclosure
  • CIA/IRO Support
  • Compliance Monitoring and Auditing
  • Fair Market Value Determination
  • Government Price Reporting
  • Litigation and Investigation Support
For more information visit, call (866) 377-0040 or contact Paul J. Silver, Managing Director, Practice Leader, (678) 672-6160.

Navigant Consulting
In the complex regulatory environment of today's Pharmaceutical, Biotech, Medical Device and Diagnostics industries, companies and their counsel face an increasing number of dispute, regulatory, compliance and investigation issues that have the potential for significant financial, economic and reputational impact. Navigant is the firm of choice when companies and their counsel need a resource who can successfully and efficiently integrate the skills of complex data management and analysis with the synthesis of highly complex healthcare transactions, rules, regulations, data, documents and business practices to bring meaningful value to the co-development of a dispute, regulatory, compliance or investigation strategy and execution.

For more information visit or contact Saul B. Helman, M.D., Managing Director, (317) 294-1228.


AHM is the leading global provider of technology-enabled services designed to manage compliant interactions with healthcare professionals for the highly regulated life sciences industry. Our patented systems are installed with the top global pharmaceutical and biotech companies and used by tens of thousands of industry sales representatives, managers and healthcare professionals. For more information visit

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 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 support our clients with respect to a wide range of US-based compliance advice and assistance, including: FCPA, trade sanctions and export controls, customs, antitrust, data protection, False Claims Act 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, or contact Michael Wagner, Chair North America Pharmaceuticals & Healthcare Industry Group, 1 (312) 861-2965.

Cooley LLP
For over 35 years, attorneys in Cooley's Life Sciences practice have played an instrumental role in the growth of many of the industry's leading life sciences companies. Our client base includes hundreds of public and private companies, based in the United States and abroad, and spans the full spectrum of industry sectors including pharmaceuticals, R&D, therapeutics, drug delivery, drug formulation, and medical devices and technologies.

We deliver an unparalleled combination of innovative legal expertise, deep industry knowledge and practical understanding of our clients' business needs. Cooley is widely recognized as a leading law firm in life sciences and was ranked Law Firm of the Year in Biotechnology by US News & World Report - Best Lawyers "Best Law Firms" in the first year the category was awarded in 2011. Cooley has a leading group of health care and life sciences regulatory attorneys who understand the challenges and opportunities facing the industry. In an environment filled with an increasing number of evolving laws and regulations, our team has the depth of experience necessary to navigate the ever changing rules of the marketplace for providers, manufacturers, suppliers, payors, technology companies and investors in this space.

Cooley's 700 attorneys have an entrepreneurial spirit, deep substantive experience, and a commitment to solving clients' most challenging legal matters. For more information, please visit:

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

Grant Thornton's Life Sciences/Pharmaceutical Practice
Grant Thornton provides audit, tax and advisory services to the life sciences/pharmaceutical industry, one of our firm's three strategic priority industries of focus. Our experience includes working with both large and small life sciences companies within the market, as well as a thorough appreciation for the nuances of different industry verticals. This translates into well-informed ideas and proven solutions that are relevant.

The people in the independent firms of Grant Thornton International Ltd provide personalized attention and the highest-quality service to public and private clients in more than 100 countries. Grant Thornton LLP is the U.S. member firm of Grant Thornton International Ltd, one of the six global audit, tax and advisory organizations. Grant Thornton International Ltd and its member firms are not a worldwide partnership, as each member firm is a separate and distinct legal entity. In the United States, visit Grant Thornton LLP at

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, PLC Which Lawyer?, 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 or contact Marketing Manager Tara Busby at (202) 637-6912.

Intuition Compliance Solutions
Since developing training for the TAP Pharmaceuticals CIA in 2001, Intuition has worked with pharmaceutical companies to design and implement regulatory and compliance training solutions that change behavior and drive compliant performance.

Over the past twelve years, we have grown to be a premier provider of pharma compliance training and communication solutions. As part of our "total solution" approach we have worked with our clients to:

  • Design and develop custom online training courses
  • Build, host, and support customized Web Portals that enable our clients to profile users and deliver, manage, and track training for agencies, CSO's, and other third parties
  • Deploy mobile apps and courses that enable field-based staff to complete required training on iPads and other devices
We've worked with six of the top ten global biopharma companies as well as small- and medium-sized companies to design and deploy solutions that support high-profile compliance initiatives. With our expertise rooted in CIA training, Intuition knows what it takes to design, develop, and deploy high quality solutions that meet the stringent content and tracking requirements of regulators.

For more information about our approach, solutions, and services please contact Dan O'Connor, Managing Director of Compliance Solutions, at (212) 686-7438.

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, uncompromising commitment to quality and dedication to understanding the business and culture of its clients. In the 2013 edition of LMG Life Sciences, ten King & Spalding lawyer have been identified as 'life sciences stars' and the firm was 'highly recommended' in the area of FDA-medical device regulatory work. The firm also retained its 'recommended' status for both government investigations/fraud & abuse and product liability matters on behalf of life sciences clients in 2013.

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

With deep industry experience, insight, and technical support, KPMG LLP is one of the largest providers of audit, tax, and advisory services to pharmaceutical and life sciences companies. We help clients gain practical insight into emerging issues, consider approaches to balance risk and controls, improve performance, and explore the accelerating transformation of this industry, both domestically and globally. For more information about KPMG, please call the KPMG Hotline at 1-877-679-KPMG (5764) or visit us at

MMIS, Inc.
Developed and marketed by MMIS, Inc., the MediSpend® Family of Products are secure hosted platforms sold as, software-as-a-service (SaaS) to meet the needs of industry, academic institutions and physicians. Developed by attorneys and IT specialists with over a dozen years of experience in health care compliance, the MediSpend® Family of Products represents the first global end-to-end compliance solution designed specifically to help pharmaceutical and medical device companies track and report HCP and HCO spend while simultaneously managing physician relationships. MediSpend® is a customizable, comprehensive, compliance platform to enable life science companies to comply with US and international transparency reporting laws.

Pepper Hamilton
For more than 50 years, Pepper Hamilton LLP ( has counseled leading pharmaceutical companies on legal matters, including regulatory compliance, government investigations and litigation. A multi-practice law firm with more than 500 lawyers nationally, the firm provides corporate, litigation and regulatory legal services to clients throughout the nation and the world.

The heart of Pepper's services to the pharmaceutical industry is our Health Effects Litigation Practice Group, which counsels clients and handles litigation involving claimed adverse effects from pharmaceuticals, medical devices, radiation, chemicals, consumer goods, environmental substances and industrial equipment. We represent clients facing investigation and prosecution by government authorities, including the U.S. Attorneys' offices, state Attorneys General and Congressional oversight committees. Our broad and deep pharmaceutical and healthcare industry experience is the cornerstone of our white collar defense and corporate investigation practice.

Our pharmaceutical lawyers work closely with lawyers in many other practice areas, including:

  • Commercial Litigation
  • Construction
  • Environmental Law
  • Health Care
  • Intellectual Property
Pepper Hamilton LLP's White Collar Litigation & Investigations team includes former FBI director and federal judge Louis J. Freeh, and a highly skilled group of former judges, federal and state prosecutors, and experienced corporate counsel. This team brings unparalleled expertise and judgment to legal representation in these areas:
  • White Collar Defense and Regulatory Enforcement
  • Corporate Investigations
  • Business Integrity, Compliance and Ethics
  • Monitorships
Our services are complemented by our alliance with Freeh Group International Solutions LLC (FGIS), an independent global risk management firm. FGIS serves a diverse range of organizations in many industries, working to reduce risk in today's increasingly dangerous and complicated global marketplace. More information about FGIS is available at and contact Thomas M. Gallagher, Partner, (215) 981-4068 for more information about Pepper Hamilton.

Polaris is a management consulting firm focused exclusively on the compliance needs of the life sciences industry. Polaris offers a suite of services that specifically target the compliance risks confronting the life sciences industries, including: compliance risk assessments, auditing and monitoring, policy and SOP development, strategic and operational solutions, aggregate spend services. In addition, Polaris Solutions has developed automated business process workflows which address medical education grants, investigator initiated trials, interactions with HCPs, exhibits, sponsorships and aggregate spend. For more information visit or contact Mark Scallon, Partner, (415) 432-4367.

Porzio Life Sciences
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, 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, 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 licensing and distribution, transparency legislation, sample and trade product distribution, and trends in government investigations.

Through our Licensing & Distribution 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.

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

Ropes & Gray LLP
We routinely advise clients on developing effective compliance policies to avoid the debilitating effects of government investigations, regulatory enforcement actions, or other litigation based on alleged noncompliance with applicable laws and regulations. Our command of FDA regulatory, health care compliance, research compliance and global anti-corruption issues is critical for clients operating in these highly regulated industries. For companies that are the subject of government investigations, our understanding of the government enforcement landscape enables us to defend complex proceedings involving simultaneous civil, criminal and administrative actions.

This depth and breadth of experience, coupled with our interdisciplinary team of leading regulatory, health care compliance, research compliance, government enforcement, and anti-corruption attorneys, has established us as the "go-to" firm when it comes to avoiding and successfully resolving government investigations. Our integrated practice, including our corporate department, also allows clients to eliminate the inefficiencies associated with hiring multiple, independent firms. For more information please visit

Sidley Austin
Sidley Austin LLP is a premier law firms with an internationally recognized life sciences practice, representing major pharmaceutical, biotechnology, medical device, dietary supplements and food clients. Sidley consistently ranks among the top firms in Asia, Europe and the U.S., and most recently Sidley is honored U.S. Life Cycle Firm of the Year by LMG Life Sciences. Many lawyers in our team are acknowledged leaders in life sciences regulatory and compliance, government enforcement and investigation, products liability, corporate, intellectual property and anti-trust matters. 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 or contact Scott Bass, (212)839-5613 and James Stansel, (202) 736-8092.

With more than 1,800 attorneys in 23 offices in the United States, Europe, Asia and Latin America, Skadden represents a broad range of clients in all sectors of the health care industry, including pharmaceuticals and medical technology. 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.


BMI SYSTEM offers software solutions for companies wishing to tackle the rapidly changing legal requirements of the healthcare industry.

Our software solutions enable your organization to meet transparency requirements regarding your relationships with HCPs & HCOs.

They are tailored to match the specific requirements of healthcare companies operating in countries with unique compliance, regulatory and transparency laws.

BMI SYSTEM software solutions facilitate the management of three critical organisational components, namely, Governance, Risk Management and Compliance.

Through the creation of bespoke solutions for a wide range of companies in the pharmaceutical, medical device and cosmetics industries, BMI SYSTEM has become the leader in the development of software dedicated to transparency and regulatory compliance.

The team, based in Paris, London, Brussels, Boston and Hanoi, has been built using a strong expertise in global healthcare regulations, software architecture and design, quality assurance and healthcare project management.

DMH BioPharm Advisors LLC
DMH is a biopharmaceutical consulting and training firm that partners with clients to develop customized solutions to integrate their commercial activities with a culture of compliance. DMH combines their substantive biopharmaceutical commercial experience at the executive and field level, to design, develop and deliver compliance training curriculum that will generate maximum engagement and translate to compliant behavior.

DMH's training materials and workshops are available for license and include a full suite of train-the-trainer, facilitator and participant guides and workshop support materials. DMH offers off-the-shelf and customized curriculum. Training content may be tailored for a learner's organizational position and responsibilities, specific brands, disease states, and market challenges.

Please visit our website at

FTI Consulting
FTI Consulting, Inc. is a global business advisory firm dedicated to helping organizations protect and enhance enterprise value in an increasingly complex legal, regulatory and economic environment. FTI Consulting professionals, who are located in all major business centers throughout the world, work closely with clients to anticipate, illuminate and overcome complex business challenges in areas such as investigations, litigation, mergers and acquisitions, regulatory issues, reputation management and restructuring. More information can be found at or contact Jayson Dukes, Senior Managing Director, (212) 499-3644.

HealthCare Appraisers
HealthCare Appraisers provides a full spectrum of valuation services and Fair Market Value solutions exclusively for the healthcare and life sciences communities nationwide:

  • Pharmaceutical and medical device companies - Compensation arrangements with physicians, researchers, allied health professionals, and others providing advisory, consulting, training, speaking and research services, as well as valuations related to intellectual property and royalty arrangements
  • Physician compensation and service arrangements including employment arrangements, on-call arrangements, medical directorships, co-management arrangements, collections guarantees for hospital-based physicians, joint venture relationships and affiliations
  • Business valuation for ASCs, specialty hospitals, long-term acute care hospitals, physician practices, imaging centers and dialysis centers, CON and other intangible assets
For more information: • (561) 330-3488

Independent Commercial Compliance™ (ICC)
Independent Commercial Compliance™ (ICC) is a full service health care compliance agency with expertise in all compliance related matters in the pharmaceutical and medical device industries. At ICC we specialize in Field Sales Force and Speaker Program Monitoring, building tailored processes to ensure effective monitoring solutions. ICC maintains an established infrastructure of over 25 qualified professionals geographically dispersed throughout the continental United States to monitor sales and marketing field activities. The geographic dispersion allows for reduced monitoring travel costs and increased client efficiencies. Further information on ICC can be found at, and contact Shawn Reardon of ICC at (908) 370-4085.

MedPro Systems
MedPro Systems is the leading provider of healthcare license and regulatory compliance solutions to the Life Science industry with over 200 customers, including 19 of the top 20 pharmaceutical manufacturers. The foundation of MedProID® is a comprehensive database of practitioner and organization licensing information obtained directly from the appropriate State Licensing Boards, for all 50 states & Puerto Rico. The MedProID® suite of products provides powerful software solutions for Practitioner License Validation, Organization License Validation, Prescription Drug Marketing Act (PDMA) Compliance, and State and Federal Sunshine Aggregate Spend reporting requirements. For more information please visit or contact Ray Ungemach, 973-398-7800.

NXLevel Solutions
NXLevel Solutions, through its PharmaCertify™ brand, provides off-the-shelf and custom commercial compliance eLearning, mobile applications, curriculum analysis, and live training workshops to the pharmaceutical and medical device industries. PharmaCertify™ solutions offer practical, real-world compliance knowledge, delivered in balance with the training goals and objectives of your entire organization. Our subject matter expertise covers the critical areas of risk for life sciences staff, including the Sunshine Act; on-label promotion; adverse events; federal and state regulations; speaker programs; and gifts and meals.

For more information about our compliance training products and services, or to see a demo, visit or contact Sean Murphy at (609) 466-2828 ext. 25.

Why settle for the standard when you can have state-of-the-art? PubsHub's suite of software applications, featuring PMSolution℠ and Journals & Congresses℠, leverage advanced technology to help you drive your medical communication initiatives at anytime, from anywhere. Upgrade to the most flexible, intuitive, and innovative solutions on the market with PubsHub.

Second City Communications (SCC)
Second City Communications (SCC) is the innovative corporate services division of the world-renowned improvisational comedy institution, The Second City. Drawing on The Second City's 50-year legacy of training the world's most famous improvisational comedians and connecting with audiences with engaging, insightful content, SCC works with hundreds of Fortune 1000 clients each year in blended learning/training programs, internal communications initiatives, meeting & event support and content marketing assignments. Our theatres and creative teams work under a defining principle of "it's funny because it's true."

RealBiz Shorts is the innovative social communication video series developed by SCC in collaboration with NYSE Governance Services/Corpedia. This subscription library of short, engaging ethics and compliance communications is designed to get attention, improve retention and change perceptions for how these important subjects are received. After all, you can't bore people into changing behavior.

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 and, or contact Simone Handler-Hutchinson, Executive Director of the Center.

The Society of Corporate Compliance & Ethics (SCCE)
The Society of Corporate Compliance & Ethics (SCCE) is a non-profit, pan-industry association dedicated to improving the quality of corporate governance, compliance and ethics.

Our magazine and e-newsletter can keep you informed about how to manage the latest issues. Come to our conferences to build out your network and hear directly from other professionals, at a discounted, members-only rate. The Compliance Academies can provide you with intensive training in the essentials of managing a compliance and ethics program. They are also excellent training for obtaining the Certified Compliance and Ethics Professional (CCEP) designation.

Can't travel? Our online social network ( provides you with online interaction with thousands of compliance and ethics leaders around the world. Or try a web conference to learn right from your desk.

To learn more about the SCCE, visit us at, and join more than 3,400 other professionals who are already members of the SCCE.

TeamMate is the solution of choice for 90,000 auditors in more than 2,200 organizations world-wide. TeamMate AM addresses key audit management functions such as risk assessment, scheduling, documentation, issue tracking, and time reporting, enabling you to standardize and streamline your entire audit process. TeamMate CM is focused on the management and testing of SOX, COBIT®, IT Governance or any other set of internal controls. CM allows you to view and interact with controls through an innovative user-defined structure based on Dimensions and Perspectives of data that leads to greater efficiency and deeper insight when managing your compliance needs. The integration of TeamMate AM and TeamMate CM promotes leveraging and sharing of data and workflows across the Internal Audit and Compliance disciplines. Learn more at

Interested in becoming a Grantor or Exhibiting?
Click Here for more information or contact Justin Sorensen at 206-452-0609.

Overview | Agenda | Promotional Opportunities | Continuing Education | Grantors & Exhibitors
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