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News Roundup: 2014 Compilation of Human Research Standards Available

Articles: How Local IRBs Can Work with Centralized IRBs

Blog Posts: Interactive Informed Consent

Marketplace: Marketplace

	2014 Edition of International Compilation of Human Research Standards Available
	IRB Services Selects IntraLinks
	Mytrus eConsent Chosen by IRB
	WRB Academy Online Learning for GCP, Research Ethics

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Applied Clinical Trials launches new e-book, Risk-Based Monitoring for Clinical Trials

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	How Local IRBs Can Work with Centralized IRBs
	RAPS: Final FDA Guidance on IRBs Illustrates Common Problems Faced in Trial Setup Phase

	Interactive Informed Consent, Better Informed Patients
	Sample Banking for Future Clinical Research

Clinical Data Disclosure and Transparency

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Corporate Translations
The preferred supplier of translations to the life science industry www.corptransinc.com

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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. Read more.

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Risk-based Monitoring Tools for Application
On Demand Webcast
To Register Free Click here.

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Editors’ Series: Monitoring Clinical Trials - Models, Myths and Momentum
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CHINA REPORT
China is the third largest pharmaceutical market in the world and will become the second largest ahead of Japan by 2015. Everything you need to know to do business in the country; key economic sector data and exclusive interviews from regional leaders. Read More.

Lisa Henderson
Editor in Chief [email protected]

SPOTLIGHT EVENT
ClinTech 2014
Mar. 11-13, 2014
Cambridge, MA
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