Compliance

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.

Learn key compliance requirements, data collection tips, and important dates for the EU Medical Device Regulation in this white paper.

Learn the full impact of PMCF under the EU MDR and how to best prepare your medical device studies.

Learn key compliance requirements, data collection tips, and important dates for the EU Medical Device Regulation in this white paper.