Watch 2-min demo
Close the consent gap — before and after study close
A consent governance layer designed to operate independently of any EDC.
Post-site closure identity verification
Centralized, multilingual consent across all versions, trials, and countries
Consent linkage to biospecimen metadata
Standalone compatibility with any EDC
Sample chain-of-custody traceability
Automated downstream updates to LIMS, biobanks, analysis pipelines
Protect yourself from consent-related exposure years after site closeout.
Post-trial withdrawals + re-consent with audit trails
Identity verification without active sites
Automated updates to biobanks and metadata systems
Eliminates reliance on site staff post-lock
Two ways to get started
During trial
Launch dynamic consent at enrollment or mid-study
Capture versioned, IRB-approved consent digitally or via paper ingestion
If a hybrid study, link participants securely while sites are active
Enable future-use and post-trial permissions upfront
Support protocol amendments and re-consent in real time
Maintain a continuous, auditable consent record from day one
Seamlessly integrate with EDC / eConsent systems
Post-trial
Re-contact participants after study close-out
Verify identity remotely without site involvement or logins
Digitize and manage legacy or paper consents
Present new consent requests for reuse, follow-up, or withdrawal
Allow participants to grant, decline, or withdraw consent anytime
Deliver real-time visibility into consent status for sponsors
Preserve a centralized, audit-ready consent record across studies and countries
Introducing the first end-to-end biospecimen intelligence solution
The Integrated Specimen Management Suite powered by Embleema & Astoriom is the first end-to-end biospecimen intelligence solution — unifying sample consent and clinical data.
Clinical, patient & sample data with consent intelligence
DIGITAL
Enrich samples with clinical & demographic metadata
Centralized consent information for sample uses across studies and countries
Participant recontact & re-consent workflows for compliance and sample reuse
Sample stewardship & global continuity
PHYSICAL
Ambient → cryo biorepository storage
Stability and biorepository solutions across the sample lifecycle
Chain of custody + compliant handling
Long-term preservation and logistics support
Sample Manager Dashboard
Real-time visibility of consent information for sample use across studies and countries
Unified clinical and sample metadata in one place
Request and obtain consent for new uses of stored samples
Unlock compliant secondary use of existing samples
Featured content
Turn patient consent into a strength, not a risk
Get a walkthrough of dynamic consent for active and closed studies.