Join RealTime CTMS to examine how paperless sites and site networks are driving quality and improved timelines for the clinical research industry.
Join Veeva Systems to explore the key qualities and features sites need to look for in their technology partners to increase their connectivity with sponsors and patients.
Join experts from Clinical Research IO to explore how several independent trends in research will make eSource a platform technology for sites.
Join The DPO Centre for this exploration of data protection challenges relating to the handling of sensitive personal data of EU and UK trial participants and how COVID-19 has bought data protection to the forefront of people’s minds.