Simple, stratified, block and minimisation. How each one allocates participants, and when to pick which.
Telemedicine, connected devices and wider recruitment. The benefits, the limits, and where DCTs are heading.
What a CRF and an eCRF hold, and how the design of the form shapes the data you end up with.
What eCOA covers, how it compares with other collection methods, and where it fits into a protocol.
What separates trial management from data capture, and which one your study needs first.
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Where real-world data comes from, the technology to handle it, and the regulatory expectations around RWE.
The benefits, the technology involved, and the CNIL rules that apply to decentralised studies in France.
The coordination, oversight and tooling that keep a study safe, compliant and on schedule.
Regulations, benefits and adoption in the field. Replay of the Datacapt webinar on electronic consent.
The regulations an EDC must meet, from 21 CFR Part 11 to GDPR and ISO 27001, and how to judge a vendor's compliance.
Collecting outcomes on patients' own devices, the effect on compliance and recall bias, and the sync back to the EDC.
Retention rules, secure archiving and controlled access, and how to arrive at an inspection ready.