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 […]
Expedite the study enrollment with Decentralized Trials
Expedite the study enrollment with DCT Decentralized Clinical Trials (DCT): Decentralized clinical trials (DCTs) are the focus point in many industry discussions and activities due to numerous benefits for patients and researchers, including high clinical trial efficiency. Clinical trials have largely traversed from site-based traditional trials to site-less DCTs, especially during the Covid-19 pandemic. But […]