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BioClinica
Risk-Based Monitoring and Related Initiatives – A Data Management Professional’s Perspective. A FREE WEBINAR presented by industry expert Jonathan Andrus. Watch the Webinar NOW.

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ACRP
ACRP Training Improves Performance – Courses Cover: Good Clinical Practice, Fundamentals, Project Management, Risk-Based Monitoring, Ethics, and More. 9 New Courses Coming January 2014! www.acrpnet.org/courses

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Medidata(CTM Monitoring)
Case study: Read how DSP Clinical improved their CRA productivity by using Medidata CTMS to streamline their site monitoring operations. [Download Now]

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BioClinica
Could you benefit from better Clinical Trials Supplies management?. Click Here for the Podcast and companion White Paper

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Implementing Rare Disease Registries: Unique Challenges & Proactive Solutions
On Demand Webcast
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Risk-based Monitoring Tools for Application
On Demand Webcast
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Drug Development Strategies in China
Pharma and biotech firms who are relative newcomers to the Chinese market aren't aware that the regulatory climate has changed dramatically in recent years. SFDA approval times for Clinical Trials Approvals have dropped to 7-9 months for small molecules. There are also opportunities in China for sponsors that have not yet completed Phase II trials to create a parallel approval strategy. Even without final details (like final dosing) it’s possible to file a CTA for Phase III based on the most current early phase results. This parallel submission strategy can shave several months off the final approval time in China. Learn more.

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IRT and EDC
The Unified Experience describes how sponsors and CROs can integrate and streamline complex processes spanning randomization, trial supply management and data collection for better clinical trials. Click here.

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Editors’ Series: Monitoring Clinical Trials - Models, Myths and Momentum
Live Webcast: December 5, 2013 at 11:00 AM EST
Register free at www.appliedclinicaltrialsonline.com/Monitoring

Lisa Henderson
Editor in Chief lhenderson@advanstar.com