National Pharma Audioconferences
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WEDNESDAY, NOVEMBER 18, 2020
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Pharma/Device Compliance Webinar: Compliance During a Crisis Series: Session II: Key Components Recommended for Compliance Programs to Thrive in a Tele-Compliance Environment


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WEDNESDAY, JULY 29, 2020
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Pharma/Device Compliance Webinar: Compliance During a Crisis Series: Session I: Have You Incorporated Tele-Compliance into Your Business Continuity Plans?


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THURSDAY, JUNE 4, 2020
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Pharma/Device Compliance Webinar: Response to COVID-19 Webinar Series: Part VI: Global Roundtable on Special Issues Raised by the COVID-19 Pandemic for Medical Device Ethics and Compliance Professionals and In-House Counsel


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THURSDAY, MAY 14, 2020
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Pharma/Device Compliance Webinar: Response to COVID-19 Webinar Series: Part V: Navigating Clinical Trials During the COVID-19 Pandemic


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THURSDAY, APRIL 30, 2020
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Pharma/Device Compliance Webinar: Response to COVID-19 Webinar Series: Part IV: Challenges Posed by Field, Commercial & Medical Personnel Change to Digital/Virtual Promotional Activities in Response to the COVID-19 Pandemic


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THURSDAY, APRIL 23, 2020
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Pharma/Device Compliance Webinar: Response to COVID-19 Webinar Series: Part III: US FCPA and Global Anticorruption Update for Pharma & Med Device


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MONDAY, APRIL 13, 2020
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Pharma/Device Compliance Webinar: Response to COVID-19 Webinar Series: Part II: Managing Pharma & Medical Device Ethics & Compliance Function Remotely


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MONDAY, APRIL 6, 2020
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Pharma/Device Compliance Webinar: Response to COVID-19 Webinar Series: Part I: COVID-19 Pandemic Action Plan for Pharma & Medical Device Ethics & Compliance Teams


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THURSDAY, SEPTEMBER 15, 2016
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Pharma Compliance Webinar: Phrma/Bio Joint Principles on Responsible Sharing of Truthful and Non-Misleading Information about Medicines with Health Care Professionals and Payers


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TUESDAY, JUNE 7, 2016
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Medical Affairs Compliance - Lessons Learned and Best Practices


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WEDNESDAY, JANUARY 11, 2012
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Analysis of the Proposed Sunshine Rule


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MONDAY, DECEMBER 13, 2010
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An Update on FCPA Enforcement in the Life Sciences Industry


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THURSDAY, AUGUST 12, 2010
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Examining the Latest Developments in Drug and Device CIAs How Corporate Integrity Agreements Continue to Reshape Compliance


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WEDNESDAY, JUNE 16, 2010
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Ten Emerging Risk Areas for Drug and Device Companies


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TUESDAY, DECEMBER 1, 2009
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Lessons of Pfizer's $2.3 Billion Off-Label Settlement


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WEDNESDAY, DECEMBER 17, 2008
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How State Attorneys General Are Reshaping Pharmaceutical Marketing and Compliance through Fraud Investigations and Settlements
Analysis of Eli Lilly's $62 Million Zyprexa Settlement and Pfizer's $895 million Bextra Settlement
A National Audioconference Sponsored by Harvard Health Policy Review and Rx Compliance Report


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TUESDAY, DECEMBER 9, 2008
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Advanced Implementation Strategies for a Compliant Grant Process


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THURSDAY, DECEMBER 4, 2008
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The Lessons of Cephalon's $425 Million Off-Label Settlement: A New Model for Off-label Enforcement


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TUESDAY, AUGUST 5, 2008
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Analyzing the Newly Revised PhRMA Code


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TUESDAY, JUNE 17, 2008
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Operating in an Uncertain Environment: The Impact of FDA's Draft Guidance on Medical Journal Reprints and Other Recent Developments


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TUESDAY, MAY 27, 2008
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Dealing with Transparency - How Drug and Device Companies are Operationalizing Disclosure of Educational Grants


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WEDNESDAY, MARCH 26, 2008
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Lessons from Merck's $671 Million Medicaid Drug Pricing Settlement


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WEDNESDAY, JANUARY 9, 2008
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Industry-Supported CME under Fire: Mitigating Risk and Enhancing Compliance


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MONDAY, NOVEMBER 26, 2007
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Lessons of BMS' $515 Million Settlement for Off-label Promotion, Kickbacks and Drug Pricing


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WEDNESDAY, DECEMBER 13, 2006
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The InterMune Off-label Settlement and the Rise of Deferred Prosecution Agreements


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WEDNESDAY, NOVEMBER 29, 2006
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How the Democratic Takeover of Congress will Impact Pharma


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WEDNESDAY, MARCH 8, 2006
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Compliance in a Highly Litigious World - Creating Good Documents and Avoiding Bad Ones


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TUESDAY, DECEMBER 6, 2005
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Global Compliance Systems: The Next Horizon for Pharma Compliance


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THURSDAY, OCTOBER 27, 2005
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Understanding the Inner Workings of FDA: - A Conversation With Peter Barton Hutt,"the Unofficial Dean of Washington Food and Drug Lawyers"


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TUESDAY, SEPTEMBER 13, 2005
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Overview and Implications of PhRMA's DTC Drug Marketing Guidelines


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THURSDAY, JULY 28, 2005
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Pharmaceutical Drug Pricing and Reporting Issues


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WEDNESDAY, JUNE 8, 2005
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Fraud and Abuse Issues for Medical Device Companies


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MONDAY, MAY 2, 2005
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The New California State Law and Other State Laws Targeting Pharmaceutical Sales and Marketing


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MONDAY, APRIL 11, 2005
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FDA's Final Risk Management Guidance: Improving Drug Safety Through RiskMAPs (Risk Minimization Action Plans)


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TUESDAY, FEBRUARY 17, 2005
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Update on the Medicare Drug Benefit and Medicare Advantage Regulations


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THURSDAY, OCTOBER 26, 2004
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The Expanding Scope of Fraud Investigations and Enforcement in Clinical Trials, Publication and Off Label Use


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WEDNESDAY, JUNE 23, 2004
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Lessons of the Pfizer Settlement for Off Label Promotion - Compliance Issues and Practices


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TUESDAY, MAY 11, 2004
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The Lessons of the Medco Settlement and Implications for PBM Regulation, Roles and Operations


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TUESDAY, MARCH 23, 2004
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Analysis of the FDA's Draft Guidance on Direct to Consumer (DTC) Advertising


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TUESDAY, FEBRUARY 10, 2004
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PBM Regulation, Investigation, Prosecution and Compliance


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WEDNESDAY, JANUARY 28, 2004
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The New Medicare-Endorsed Prescription Drug Discount Card Program: How it Will Work and Who Will Participate


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WEDNESDAY, JANUARY 14, 2004
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The Implications of the New Medicare Prescription Drug Legislation for Pharmaceutical Manufacturers, PBMs and Health Plans


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THURSDAY, OCTOBER 16, 2003
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The New Risk Area - Internal Investigations in a Post Sarbanes Oxley World


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THURSDAY, OCTOBER 2, 2003
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Off Label Promotion - Compliance Issues and Practices


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THURSDAY, SEPTEMBER 18, 2003
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Operationalizing the OIG Pharmaceutical Guidance - Grants, Consulting Agreements and Sales and Marketing


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WEDNESDAY, MAY 21, 2003
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An Analysis of the New OIG Model Compliance Guidance for the Pharmaceutical Industry


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TUESDAY, OCTOBER 22, 2002
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An Analysis of the New OIG Model Compliance Guidance for the Pharmaceutical Industry


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TUESDAY, OCTOBER 8, 2002
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The Implications of New Corporate Governance Rules on Compliance in the
Pharmaceutical Industry


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WEDNESDAY, MAY 29, 2002
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HIPAA for Pharmaceutical Manufacturers, PBMs, and Pharmacies


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