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news roundup
Cerner Corporation is offering select U.S. health systems and academic research centers complimentary access to critical de-identified COVID-19 patient data to help fight the pandemic.
PHARMASEAL is expanding the capability of the Engility platform. Electronic trial master file document(eTMF) storage is now available alongside Clinical Trial Management in the same integrated platform.
Pharm-Olam developed a 12-week program, Core Global Competencies for Clinical Research Auditing, which IACOR has independently accredited to ensure consistently high standards of clinical research auditing across the industry.
There is still time to register and participate in the virtual The 2nd Annual Medical Hero Appreci-a-thon to express appreciation for all “Medical Heroes”—medical and healthcare professionals, researchers and study volunteers.
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In this article, the author proposes a risk-balanced approach to outsource clinical studies, which requires both parties to be transparent, objective, and work collaboratively early in the outsourcing process.
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In this interview, Ravi Jandhyala, consultant pharmaceutical physician at Medialis and an expert in rare disease patient registries, discusses how to overcome clinical trial registry challenges.
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Blog Posts
COVID-19 will not only leave a long legacy on public health, but it may also force companies that have been lagging behind the disruption curve to adopt technologies and processes that will make clinical trials more efficient.
Vivienne van de Walle, MD, PhD, CPI, FAPCR is co-founder and owner of PT&R (PreCare Trial & Recruitment), an independent research site in The Netherlands, and has been an advocate for virtual site visits over the past five plus years. Read more about her thoughts on virtual trials.
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