White Papers

May 04, 2017
Sponsored Content
Oncology trials are undeniably complex. Discover how you can successfully mitigate risks and maximize trial success by creating a comprehensive strategy that plans for the differences in immunotherapy development and proactively monitors execution.
Apr 25, 2017
Sponsored Content
By Oracle
ACT’s 16-chapter video series captures conversations with both user and vendor experts about RTSM and IRT and the hottest trends affecting this important market segment. Learn about how systems are being improved to keep up with today’s needs for efficient clinical trial management; how new tools can help companies be more proactive in managing their trials; the benefits of configurable systems, and more.
Apr 24, 2017
Sponsored Content
Data insights in real time, all the time? That’s just one of the benefits of a modern approach to clinical data management. Clinical teams can run the trial they want – collecting data from all areas of research to make better, more informed decisions. No longer are teams burdened with inflexible systems that silo data and are unable to support the complex trials needed in today’s market.
Apr 14, 2017
Sponsored Content
As technology advances and with Good Distribution Practices (GDP) regulations constantly changing, delivering quality product to patient comes with its challenges and costs.
TempEZ™, part of Almac’s Next Generation Temperature Management Solutions, provides life science companies with an end to end regulatory compliant solution, giving full visibility of your temperature data from any stakeholder within your supply chain. It ensures product quality and integrity from manufacture through to patient administration.
Find out more about this next generation innovation by listening to Almac’s temperature management expert, Heather Bogle, Supply Chain Solutions Manager as she guides you through how TempEZ™ can help tackle these changing GDP regulations.
Apr 11, 2017
Sponsored Content
Clinical trial sponsors face many disclosure risks as they register trials and report results information to worldwide registries and health authorities. Most don’t know how they are performing against local laws or internal policies. Atlas Global Compliance mitigates these risks, providing early insight into global disclosure performance.
Apr 04, 2017
Sponsored Content
Mobile apps are an important link between researchers and patients, but using them in clinical development requires rigorous preparation. Download this white paper to learn more about data strategies for mobile apps throughout the trial life cycle, the current and future regulatory environment, and how to provide deeper patient engagement.
Apr 03, 2017
Sponsored Content
QuintilesIMS, with Bristol-Myers Squibb, shares insights on the evolution of the regulatory affairs profession and industry, including significant technology enhancements. Examine the shift of regulatory affairs to local hubs and how it is creating opportunities for regulatory professionals to work directly with regulators providing thought leadership and supporting product development.
Apr 01, 2017
Sponsored Content
A key step in translational science is the move from animal and other preclinical studies to initial human testing. Discover how our experts help to reduce uncertainty for FIH trials.
Apr 01, 2017
Sponsored Content
Discover a hassle-free, customized integration solution that is leading the industry to a new and better way of reliably transferring site and user information automatically.
Apr 01, 2017
Sponsored Content
FIH studies that need to include woman will find that successful enrollment is achievable with the correct strategies. This paper explores challenges in recruiting women and strategies for improving the recruitment rates.
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