How to improve patient compliance in your medical device study
Here’s an idea that will make you slap your forehead.
You can just stop transcribing case reports on paper.
FDA eSource guidance recommends direct data entry into your EDC. The eCRF becomes electronic source and you eliminate source document verification.
You save money, systems, time and you get to go home early.
Don’t let people confuse you with all kinds of complicated scenarios just because they’re selling systems.
Check out my blog post on Why merging medical records and clinical trial data is a very bad idea and see how merging EMR and clinical trial data can expose you to data breaches and endanger your clinical trial success.
Just keep it simple.
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