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news roundup
A recent analysis finds that pre-market development time for breakthrough-designated drugs is 2.2 years shorter than for those without.
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Immuno-Oncology Insights:
Top 5 Challenges in Today's Immuno-Oncology Trials
On Demand
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The Covance Central Laboratory in Geneva provides services for global clinical trials in Europe and Africa.
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Overcoming regulatory and statistical hurdles of biosimilars drug development
Designing smarter trials
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Agreement combines PAREXEL’s LIQUENT InSight RIM platform and EMC's Documentum.
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Mitigating risk using Risk-based Monitoring
On Demand
Learn how risk-based monitoring (RBM) is transforming clinical development by mitigating risk while optimizing execution. Understand how to achieve enhanced patient safety with improved quality to execute your RBM studies with confidence.
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Updated people moves and company awards.
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Blog Posts
Mike Graziano, VP of Toxicology at Bristol-Myers Squibb, will elaborate on Biocelerate's toxicology data sharing initiative.
Pharmacists have new prominence in a new European system, created jointly with drugmakers and wholesalers and parallel traders.
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mHealth
There has been an increased interest in the potential of e-health and m-health in low- and middle-income countries.
A significant increase in usage of wearables and devices to collect patient data in clinical trials is likely as these devices can provide data such as mobility, sleep, heart rate that would otherwise be unavailable.
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Articles
Governments and patient advocate organizations can incentivize pharmaceutical companies that engage in orphan drug development.
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