22 results
How do you cope with data protection and data privacy in your database?
Case study – Ambulatory ECG analysis and reporting for arrhythmia detection
View this webinar to learn how staicy can integrate seamlessly your internal and external clinical applications and utilize her proprietary functionality to uniquely select geographical storage location for your data.
How will the new EU General Data Protection Regulation (GDPR) affect my clinical trial?
Digital health
How do you guarantee to deliver high-quality data at the end of your trial?
The main goal of any EDC solution is to be secure, user friendly and customized to fit your specific trial. View this webinar and find out how easy it is to build an eCRF with edc2go.
US Food and Drug Administration medical device regulators have published new draft guidance recommending proper use of electronic records and signatures in clinical investigations. The new guidance applies to clinical trial sponsors and investigators as well as Institutional Review Boards (IRB) and clinical research organizations (CRO) that must comply with 21 CFR Part 11 regulations pertaining to electronic records and signatures.
From data to insights in minutes
The pharmaceutical and medical device industries continuously look for opportunities to effectively and efficiently manage data collected in clinical trials to deliver meaningful treatments to those in need. A fundamental requirement for informed decision-making and reliable performance reporting is the consolidation of all collected information, often heterogeneous and disparate, into one location where they can be linked together for analysis.