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Windhover and IN3 Webinars, divisions of Elsevier Business Intelligence, have served more than 3,000 participants with insightful, thought-provoking and action-oriented discussions of out industry -- straight from the minds of those in the know. And more than 300 of our insightful webinars are available for purchase or complimentary download.

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Archived Webinars

Previous webinars are available for purchase via digital download and contain the original audio in Windows Media® format with accompanying presentation slides (when applicable) in Adobe® PDF format.

2010


February 11, 2010 - Capitalizing on New FDA Guidance: The Promise and Perils of Disseminating Scientific Literature About Off-Label Use of Medical Devices

January 21, 2010 - FDA's Enforcement Initiative: What should you do differently?

January 20, 2010 - The Road to FDA Approval: Advisory Committee Survival Strategies

2009


December 15, 2009 - Public Interest/Private Sector: Collaboration and Conflict in Drug Development

December 11, 2009 - Avoiding the 14 Biggest Mistakes Made by Emerging Life Science Companies in Reimbursement, Valuation, Investor Presentations and Regulatory Strategy

December 9, 2009 - Patient Registries: Integrating New Requirements and Evolving Best Practices

November 24, 2009 - Dealing with Payors: Creative Strategies to Optimize your Drug's Positioning & Reimbursement

October 21, 2009 - Pfiguring Out The Pfizer Settlements

October 14, 2009 - Biotech and Pharma Dealmaking in the Era of Uncertainty

October 1, 2009 - FDA Requirements for Training at Device Facilities: Are you in compliance?

September 30, 2009 - Product Liability: Strategies for Success when Medical Technology and Life Sciences Companies Come Under Attack

July 22, 2009 - FDA Requirements for Device Software: Are You in Compliance?

June 4, 2009 - How to Transform Your Commercial Strategies for Success in the 21st Century

May 20, 2009 - How to Navigate Changing Trends in DTC Advertising

How to Compete in the Brave New World of Follow-on Biologics

April 23, 2009 - Part II: Product Development Strategies for Follow-on Biologics

February 5, 2009 - Part I: Preparing for the Changing Regulatory Landscape of Follow-on Biologics

April 21, 2009 - Comparative Effectiveness Reaches the US: What Can We Learn from NICE?

Pharma Business Strategies for Biomarkers Series

April 9, 2009 - Cancer Biomarkers: Case Studies in Lessons Learned and Experiments in Process

April 2, 2009 - Clinical Case Studies: How Biomarkers Can Help Make a Go/No-Go Decision about Proceeding with a Drug Development Program

March 26, 2009 - Is There a Business Model for Companion Diagnostics?

March 19, 2009 - Biomarker Data’s Influence on Reimbursement: How Can Payors Use Biomarkers in Coverage Decison-Making?

February 19, 2009 - Are Biomarkers the New Requirement for Dealmaking?

February 20, 2009 - How to Prepare for Pricing & Reimbursement Reform in China

January 30, 2009 - Overhead at the J.P. Morgan Healthcare Conference: Key Unbiased Take-Aways for Your Whole Team

January 29, 2009 - Vaccines: Is the Boom Sustainable During the Obama Era

January 21, 2009 - How to Prepare for the EU’s Sweeping New Pharma Legislation

2008


December 16, 2008 - The Chinese Regulatory Outlook — A Changing World for Drug and Device Companies

November 20, 2008 - Webinar: Succeeding in High Potential Markets

November 13, 2008 - Webinar: REMS: The New FDA Post-Market Safety Restrictions for Drugs... AND Devices

October 15, 2008 - Webinar: U.S. FDA Inspections in China

October 7, 2008 - Webinar: PhRMA Code Revisions: The Implications of the Revised PhRMA Code on Industry Policies and Processes: Implementing the Changes

September 16, 2008 - Webinar: Grassroot Strategies for Improving Patient Access to Innovative Medical Technology

September 9, 2008 - Webinar: Change-of-Control Provisions: Great Protection or Traps for the Unwary?

August 27, 2008 - Webinar: Anti-Bribery Compliance in China – Avoiding the Pitfalls

July 17, 2008 - Webinar: Reviving the Primary Care Market: Strategic Considerations and New Growth Alternatives

July 10, 2008 - Webinar: The Road to FDA Approval: Advisory Committee Survival Strategies

June 26, 2008 - Webinar: How To Maximize Your Reimbursement Value Through Pharmacoeconomic and Outcomes Research: Adapting to the Changing Dossier Environment

June 12, 2008 - Webinar: Managing Current Challenges to Ensure Future Growth

May 22, 2008 - Webinar - "The Secrets to Creating an Effective VC/Investor Presentation: What Every Investor Wants to Hear from You!"

March 12, 2008 - Webinar - "Medical Devices: Surviving the New World of Government Investigation, Enforcement and Settlements"

January 31, 2008 - Webinar - "4th Annual Overheard at JP Morgan/H&Q: Key, Unbiased Take-Aways for Your Whole Team "

For more information or to register for these insightful and interactive webinars, please contact:

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Email: a.riley@elsevier.com
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The IN VIVO Blog

IN3 Europe + Investor Day
April 28-30, 2010 · Paris, France

IN3 East + Investor Day
June 9-11, 2010 · Boston, MA

Euro-Biotech Forum
June 28-30, 2010 · Paris, France

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Orphaned No Longer: Big Pharma Embraces Drugs for Niche Markets
Hit hard by late stage pipeline failures and the regulatory and reimbursement challenges of traditional primary care products, Big Pharmas are taking renewed interest in drugs for orphan diseases, where high unmet medical need offers the promise of premium pricing and there's potential to grow the market via approval in multiple indications. . . [MORE] (IN VIVO)

Despite Advances, Regenerative Medicine Faces Funding Crisis
Stem-cell and regenerative medicine firms are scrambling to find business models to harness the field's nascent, rapidly evolving science. Companies deep into clinical trials are still looking for pharma partnerships. . . [MORE] (Start-Up)

The Future of Drug-Eluting Stents Part II: Biodegradable Platforms
The safety profile of drug eluting stents appears to be improving with second and third-generation designs that utilize thinner struts (which are believed to reduce vessel injury and turbulent blood flow) and minimize or eliminate the polymer coating. . . [MORE] (Medtech Insight)

Health Reform in the Balance: What It Means for Biopharma
The long road to enacting health reform appeared to be close to an end with final negotiations taking place in the White House. But the Senate race for Ted Kennedy's open seat in Massachusetts has put the bill, and pharma's hard-fought concessions, in the breach. . . [MORE] (The RPM Report)

Read more from the latest: IN VIVO, Start-Up, The RPM Report, Medtech Insight, "The Pink Sheet", "The Pink Sheet" DAILY, "The Rose Sheet", "The Tan Sheet", PharmAsia News, Pharmaceutical Approvals Monthly, and "The Gray Sheet".




Pharma Deals
  FDA Has Full Plate This Fall for Vaccines: More Than H1N1
  GSK Slides Away From Innovation
  The Billion Dollar REMS: Xenazine?
Device Deals
  Stroke Devices: Facing Challenges Head On
  Vascular Closure Devices at the Crossroads
  What New Her2 Tests Say about Personalized Medicine

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