Elemental IRB
Ethics, faster.
Log In Sign Up
← Back to Glossary
Glossary Term

Source Documents

Clinical Operations

Also known as: source data, source records

Original records of clinical findings, observations, and other activities in a trial, used for reconstructing and evaluating the trial.

Source documents include hospital records, lab printouts, ECGs, signed consent forms, pharmacy records, and investigator notes. Data in the CRF must be traceable to source documents (ALCOA principles).

Need IRB review for your study?

Elemental IRB provides fast, transparent ethical oversight for commercial and academic research.

See pricing →   How it works →