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Bring existing study media into ACAM

ACAM imports recordings, documents, scanned assessments, and media libraries from Zoom, Dropbox, and AWS S3, then routes them into compliant processing, review, and audit workflows.

Migration should not slow down adoption

Many clinical teams already have valuable recordings, scanned forms, and study files stored outside their EDC. ACAM helps centralize those assets into a compliant workflow so teams can start with the data they already have.

Zoom Dropbox AWS S3
Import Queue
Session_PT0142_W12.mp4
Imported ✓
Interview_PT0089_W8.mp4
Processing ⟳
Assessment_PT0201_W4.pdf
Transcript Ready
Review_PT0156_W16.mp4
Review Pending

Connect the sources your teams already use

Zoom

Import remote assessment recordings and interview media for transcription, playback, review, and traceability.

Dropbox

Ingest study folders, scanned assessments, PDFs, images, and media files into ACAM workflows.

AWS S3

Connect existing S3 media libraries or backups and route source assets into ACAM processing and review.

From external source to compliant review

Connect Source Zoom, Dropbox, or AWS S3
Select Files Choose recordings and documents
Map Context Study, site, participant, visit
Import Queue Track import progress
Process Convert, transcribe, extract
Review Available for clinical review

Imported media becomes part of the clinical study record

ACAM helps imported files become clinically meaningful by associating them with the right study context and downstream review workflow.

Study
Site
Participant
Visit
Assessment
Session

Designed for easier onboarding

Faster migration

Bring existing study assets into ACAM without rebuilding from scratch.

Centralized review

Review new and historical media in one controlled platform.

Reduced manual transfers

Avoid repetitive download, rename, upload, and tracking work.

Unified compliance controls

Apply ACAM traceability and audit workflows to imported data.

Ready to modernize clinical assessment data capture?

See how ACAM helps your team capture new clinical data, import existing study media, process recordings and documents, support reviewers, and maintain compliance across regulated study workflows.