Embleema Study Coordinator App
What should I do in the Study?
How do I generate a manifest for my bio-samples shipment?
What do I need to do once I have collected the laboratory samples?
I made a mistake in an eCRF but cannot edit it anymore, what should I do?
What is PHI (Protected Health Information) and PII (Personally Identifiable Information)?
How should I handle sensitive information such as Personal Identifiable Information (PII)
Can I fill my participants' PRO surveys with them during a visit?
How do I visualize my participant's response to PRO surveys?
I submitted an eCRF and I can't edit it anymore, is this normal?
I have a site query from the Central Study Coordinator, what should I do?