QuintilesIMS Blog

Fresh ideas and insights from our experts around the globe

How automation, harmonization and outsourcing are changing the way the industry conducts pharmacovigilance.
Karen Knecht
Becoming familiar with the new MACRA Quality Payment Program (QPP) is a first step in undertaking the implementation of its complex requirements.
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Chris Bamford
How Regulation 536/2014 will impact the way developers conduct research in the EU.
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Kenric England
The importance of stage gate reviews to good clinical research project management.
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Ray Huml
A look at the six challenges companies face when pursuing this potentially lucrative development path.
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Annie Bing
When clinical research sites join networks, they can leverage the expertise of the collective, generating real benefits for sponsors.
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Sylvie Dupin
On dealing with the unpredictability of seasonal studies.
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Barbara Gillespie
A follow-up report on the CardioVascular Clinical Trialists Forum, and the opportunities to enhance collaboration between cardiologists, endocrinologists, and nephrologists for the benefit of patients with chronic kidney disease.
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Lana Pauls
A look at the FDA’s approach to using social media to track and manage adverse event reports.
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Catherine de Castro
How QuntilesIMS is building an army of project managers ready to tackle every risk that comes their way.
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Marie Lux
How patient-driven study design reduces the barriers to trial participation.
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