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news roundup
Results show that large molecules continue to outperform small molecules, particularly in the early phases of development.
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FREE eCLINICAL CASE STUDY
Learn how a global life sciences organization quickly and efficiently rolled out multiple eClinical–based research studies...several in just a few days…saving them substantial time and decreasing costs by >50%.
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Medidata announced that Techfields Pharma has selected its Clinical Cloud solution to power a Phase II ischemic stroke study.
For the third year in a row, Veeva Systems' 2016 Paperless TMF Survey: CRO Report shows trial master file (TMF) owners shows an increased use of eTMF solutions among CROs, as well as other benefits.
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Partnerships in Clinical Trials USA 2016, celebrating its 25th year. October 5-7 / Boston Convention Center. Push Novel Drugs to Market through Clinical Trials Innovation, Technology and Strategic Relationships. Spotlight session on Zika.
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Vote now and at the end of the month, we will provide your answers with expert analysis.
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New challenges in pharmacovigilance – preparing for ICH E2B (R3) and IDMP implementation
Live Webinar: Wednesday September 21 at 11:00 AM EDT
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Articles
Nearly one year has passed since CFDA was pushed to accelerate its activities to promulgate new or updated regulations and guidelines, and those reforms are rebuilding smoother processes for innovative drug development in China.
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 Click here to watch a short video about Covance's Xcellerate Forecasting & Site Selection tool, which helps forecast study timelines and supports selection of optimal investigator sites.
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Beyond any general economic considerations, what might the new reality facing the country and the European community be after Brexit, and, how will the changes impact the pharmaceutical and life sciences industry? |
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Drive better outcomes with improved trial design
Live Webinar: Tuesday, December 6 at 11am EST
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Blog Posts
Gastroenterologists across the U.S. frequently see patients diagnosed, or misdiagnosed, with GERD and are dissatisfied with PPI treatment. Frequently, the wrong endpoints in trials are the culprit. |
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Regulatory Changes in India and What It Means for Clinical Research in the Country
Live Webinar: Wednesday, October 19 at 11:00am EDT
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Oncology
A joint meeting in Brussels of the European Organization for Research and Treatment of Cancer, the US National Cancer Institute, the EMA, and the American Association for Cancer Research, responds to the perceived need for multi-stakeholder collaborations in oncology drug development.
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Simplifying the complexities of global rare disease drug development
Live Webinar: Thursday, September 15 at 11:00 EDT
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A tricky issue for clinical research sponsors is to decide which individuals should have priority access to drugs in limited supply.
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Optimizing real-world evidence programs to generate value
Tailored approaches for emerging biopharma
Live Webinar: Wednesday, September 14 at 10:00am EDT
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Many new solutions to find patients for clinical trials use technologies around biomarkers and EHRs in the oncology space. |
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Transforming Patient Recruitment through Patient and Site Engagement
On Demand
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