How will the new EU General Data Protection Regulation (GDPR) affect my clinical trial?
How do you cope with data protection and data privacy in your database?
Case study – Ambulatory ECG analysis and reporting for arrhythmia detection
How can staicy capture, analyze and report data of a wearable medical device?
We produce unprecedented quantities of data on a daily basis and it requires a solid data management platform to process and visualize this data. View this 30 min. webinar to better understand how staicy brings health and research data together and delivers insightful, actionable analytics.
How do you guarantee to deliver high-quality data at the end of your trial?
How can staicy empower patients and support Patient Reported Outcomes?
How can staicy’s EDC and dashboard technology help manage your study?
US Food and Drug Administration medical device regulators have published new draft guidance recommending proper use of electronic records and signatures in clinical investigations.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.