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news roundup
Cenduit’s division will provide hands-on experience for managing and enhancing Interactive Response Technology (IRT) systems.
The 200 investigators provide care to approximately 600,000 kidney disease patients.
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CBI's Clinical Technologies Conference, taking place this March in Philadelphia.
CBI's Clinical Technology Congress offers the opportunity for clinical executives to gain insight into utilizing technology to enable efficient, cost-effective trials while maintaining data control. With a focus on process and data stewardship, attendees walk away with best practices to streamline trial execution through enabling technology at the sponsor/CRO, research site and patient level
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The changes will enable study sites to access central lab data in real time, improve inventory management and order tracking, facilitate patient management and safety and more.
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Regulatory
An investigation published by The BMJ has raised concerns from the U.S. and European regulators about the validity of a pivotal trial.
The French national drug safety agency released the timeline of events for the Phase I clinical trial of BIA 10-2474.
With clinical research expert Robert Califf slated to take the helm of the agency, initiatives to streamline trials will be a prime area of focus.
The new approach adopted by the EMA's Pharmacovigilance Risk Assessment Committee builds on existing activities in the member states and the agency.
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Articles
A survey conducted in Germany has shown that in the pharmaceutical environment, the number of SOPs and related documents is increasing.
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Inn the world of clinical research, the data privacy threat is one that was raised long ago and mitigated by regulatory agencies.
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