Webinars, Workshops & Virtual Conferences

WEBINAR

Metrics for an FDA-Compliant Quality System: CAPA, Complaints, Supply Chain, Design and Validation

May 22, 2012 - 1:00PM ET / 10:00 AM PT

cGMP Compliance for Phase 1 IND: An Intermediate Level Discussion

May 10, 2012 - Webinar

Medical Device Adverse Event Reporting Requirements from Clinical Trials to Post-Marketing: EU, Canada and US?

May 8, 2012 - Webinar

Patent Reform Strategies in the Life Sciences: Assessing "First-to-File" and Freedom to Operate Under the New Rules - (Sponsored by MERRILL DATASITE®)

May 2, 2012 - Complimentary Webinar

The New U.S. Sunshine Act: Impending Changes For Industry and Health Care Providers

April 26, 2012 - Webinar

Stop the Frustration: 5 Keys to Leading a Great BioPharma or Device Sales Team

April 25, 2012 - Webinar

Training Your Trainers: Effective and Compliant GxP Training Strategies

April 24, 2012 - Webinar

FDA Process Validation Final Guidance: Discover Lessons Learned One Year Later

April 5, 2012 - Webinar

Developing Effective Quality Agreements: Legal and Regulatory Issues in 2012

April 3, 2012 - Webinar

FDA's Current Thinking on Biosimilar Products

March 22, 2012 - Webinar

Reimbursement Basics: What You Need to Know To Answer Investor Questions

March 15, 2012 - Webinar

Current Trends in EU's Evolving Regulatory Environment for Medical Devices and IVDs

March 1, 2012 - Webinar

Breaking through the Fog: How NOT to Kill your Presentation with your Slides

February 28, 2012 - Webinar

Outlook for the Biomedical Industry in 2012: What's Affecting Innovation? - Sponsored by Merrill Datasite ©

February 15, 2012 - Complimentary Webinar

Developing a Compliant Data Trending System: FDA Demands & Quality Issues

February 9, 2012 - Webinar

Medical Device Complaint Handling: What the FDA Wants to See (and How to Show Them)

February 7, 2012 - Webinar

Cleaning Validation: Best Practices for Maintaining a Compliant Global Program

January 24, 2012 - Webinar

Accountable Care Organizations: What You Need to Know Now!

January 17, 2012 - Webinar

Market Access in the Era of Specialty & Biotech (An Elsevier Business Intelligence Webinar in Partnership with inVentiv Health)

December 13, 2011 - Virtual Conference

Human Factors: Navigating the Regulatory Trenches, New Guidance and Usability Requirements

December 6, 2011 - Webinar

China's New 2020 Approach: Rewriting the Rules of Competition in 2012 and Beyond

December 1, 2011 - Webinar

Bridging the Gap Between the Sell- and Buy-sides in BioPharma Business Development
Sponsored by MERRILL DATASITE®

November 29, 2011 - Complimentary Webinar

Managing Your CAPA Program: Building and Utilizing Risk Assessment Tools

November 17, 2011 - Webinar

Clinical Outsourcing: Effective Partnering and Quality Management Strategies

November 8, 2011 - Webinar

The 5 Cs of Good Medical Writing for Pharmaceutical and Medical Device Professionals

November 1, 2011 - Webinar

Navigating FDA's Latest Draft Guidances on Clinical Trials and Benefit-Risk
Sponsored by MERRILL DATASITE®

October 25, 2011 - Complimentary Webinar

Real-World Strategies for Conducting Successful Root Cause Analysis

October 20, 2011 - Webinar

FDA Social Media Guidance: Hey, What's the Problem?

October 5, 2011 - Webinar

The Promise and Perils of Disseminating Scientific Literature: Avoiding Off-Label Use

September 28, 2011 - Webinar

Validating Excel Spreadsheets: A Detailed Roadmap to Compliance

August 18, 2011 - Webinar

Biosimilars & Biobetters: Market Access Opportunities and Regulatory Challenges

August 17, 2011 - Webinar

Functional Food Claims: Avoid Potential Pitfalls or Get Snared by the FDA and FTC

August 16, 2011 - Webinar

Responding to Form 483s: Learn from a Former FDA Device Investigator

July 19, 2011 - Webinar

Off-Label Promotion: Dos and Don'ts for Monitoring and Maintaining Compliance

July 12, 2011 - Webinar

Billing Medicare for Clinical Trials: What Sponsors Need to Know

June 29, 2011 - Webinar

Demystifying the BioPharma Landscape in India: Opportunities and Challenges

June 16, 2011 - Webinar

Electrical Device Compliance: Meeting IEC 60601-1 Third Edition Requirements by 2012

June 14, 2011 - Webinar