Electronic Patient Reported Outcome (ePRO)

AKRN Scientific Consulting, a medical device CRO, used Castor’s flexible EDC solution to handle constant mid-study changes for their client.

Castor is shifting the research paradigm for eCRF in clinical trials, transitioning from old, inefficient processes to a comprehensive CDMS & DCT platform.

Registry studies focused on a specific medical device are a valuable tool to capture the safety and outcomes of the device over its lifetime. Read more here.

Patient reported outcome measures in clinical trials have traditionally been done on paper. Surveys are a common way…

Clinical trials are experiencing significant disruption worldwide due to the COVID-19 pandemic. Medical research is not immune to…

As of early April 2020, over 1,000,000 people have been confirmed infected with the SARS-CoV-2 coronavirus, and governments…

Patients suffering from arthralgia at risk of an inflammatory rheumatic disease depend on an appropriate referral. But general…

Respiratory syncytial virus (RSV) is the secondary cause of death after malaria for children <5 years of age…

Dexamethasone is a synthetic glucocorticoid used by patients for immune-suppressive effects. But the drug can have severe side…

To ensure ongoing regulatory compliance under the EU MDR, medical device manufacturers must demonstrate the safety and performance…