eConsent Readiness in 12 Countries
eConsent is imperative for continuing research during the COVID-19 pandemic and beyond, but regulations can vary widely across borders. Download this whitepaper to learn the regulatory stances of 12 countries on the use of eSignature and eConsent in clinical trials.
Demystifying CDISC standards in the modern era of Decentralized Clinical Trials
Learn key compliance requirements, data collection tips, and important dates for the EU Medical Device Regulation in this white paper.
Essential Guide to Post-Market Clinical Follow Up (PMCF) Data Collection for Medical Device Manufacturers
Learn the full impact of PMCF under the EU MDR and how to best prepare your medical device studies.