EDC

One is very common, the other is rarely granted. Learn the key differences between waiver of consent & waiver of written consent for clinical trials

eConsent plays a pivotal role in optimizing modern clinical trials, but the nuance around its adoption for pharmaceutical and medical device companies remains a consideration for implementation teams.

In this blog we cover how eConsent benefits trials and aligns with IRB ethical commitments, how to prepare your IRB submission for approval, and the future impact of large language models on the informed consent process.

An avalanche of data from so many real-world sources is available today, with the promise of more data generated daily—so why not use it?

Castor’s ePRO solution enabled AKRN and Company Z to engage with a participant population that, on their own, might struggle with a technology solution that they’ve never used before.

An electronic data capture (EDC) system is software used to collect, clean, transfer, process, and store data in clinical trials. EDCs are used by contract research organizations (CROs), sponsors, and sites to conduct both simple and complex clinical trials in all phases of research.

Learn how AKRN and Company Y were able to complete their 100-person study in nine months to help test the effectiveness of their PVI analyzer in confirming PVI results.

AKRN Scientific Consulting, a medical device CRO, used Castor’s flexible EDC solution to handle constant mid-study changes for their client.

For successful decentralized clinical trials, researchers must encourage patient engagement. Learn 5 steps that modern companies are taking for better outcomes.

Castor’s eSource platform streamlined collecting, capturing & processing large amounts of clinical data to train AusculThing’s AI algorithm.