How eConsent helps the site
How eConsent helps the site and comply with the GCP Generally, informed consent (IC) is a process that educates a participant about all the aspects of a given procedure or trial, such as risks, benefits, and alternatives, so that the participant is competent to make a voluntary decision about whether to participate in the procedure […]
How to optimize the study startup (SSU)
Study Startup (SSU) – which encompasses various critical steps required to start a study – is an inherently complex process with typical roadblocks. Given that the work involves professionals and experts across different locations and at various levels – sponsor, Contract Research Organization (CRO), and onsite, the initial scope of Study Startup (SSU) is hard […]