by Mednet | Aug 25, 2020 | Blog
We recently had a chance to catch-up with Jean Brislance, Senior Quality Compliance Engineer, to learn more about the work he is doing at Mednet and his thoughts on the challenges and opportunities for clinical trials. Jean’s role at Mednet is a critical one – he...
by Mednet | Aug 13, 2020 | Blog
The clinical trial industry continues to experience rapid change. The increasing complexity of trial designs, growing pressures to build and execute more quickly, and demands for new automation and new data sources are driving technology decisions. As new technologies...
by Mednet | Aug 6, 2020 | Blog
The COVID-19 pandemic has led to numerous changes in the way we conduct clinical trials. Health authorities, sponsors, and CROs have rallied to keep clinical research moving forward as research teams, site personnel, and trial participants find themselves in various...
by Mednet | Jul 28, 2020 | Blog
Looking across the pharmaceutical, biotech, and medical device industries, we can see many different changes to how trials are being conducted during the COVID-19 pandemic. The pandemic has highlighted the importance of some existing needs and created new requirements...
by Mednet | Jul 21, 2020 | Blog
The medical device industry, like most industries, has felt the repercussions of the COVID-19 pandemic. Medical device teams have always had to face the “hurry up and wait” dynamics of moving complex diagnostic and therapeutic innovations through even more complex...
by Mednet | Jul 14, 2020 | Blog
As the clinical research industry works to find new ways of operating during the COVID-19 pandemic, one of the groups feeling increased pressure to perform are Contract Research Organizations (CROs). Our CRO partners across the industry are striving to manage the...
