Researchers
Human Skin Samples
A Non-Invasive Approach To Epidermal Sample Collection
Skin Specimen Collection
Skin taping has gained popularity as a non-invasive approach to epidermal research as it offers many of the same benefits of collected skin biopsies, but without the discomfort associated with the procedure. Sanguine utilizes skin taping procedures in conjunction with our direct-to-patient model to collect skin samples directly within the patient home.
Our unique patient-centric engagement model enhances the accuracy and timeliness of information on health status, disease activity, and other patient data so you can make informed study design decisions and conduct your research confidently.
Looking for other sample types? We can deliver several other human biofluids and tissue samples, such as whole blood, PBMCs, serum, and stool.
Why Sanguine
Our patient-centric approach translates into an enhanced ability to recruit and retain study participants, enabling access to difficult-to-reach patient populations and challenging sample collection timepoints.
Longitudinal and event-based biospecimen and data collection
Same-day sample collection and delivery
Nationwide patient member community to meet complex inclusion/exclusion criteria
Medical record-verified eligibility and pre-screening
Access to electronic medical records, health histories, patient-reported datasets
Long-term follow-up with study participants
We Specialize in These Conditions
Behind our therapeutic experience are patient member communities made up of more than 60,000 total members ready to advance science and medicine for the conditions they live with.
Get Samples for My Research
Compliance & Quality Assured
Sanguine utilizes two internationally-recognized IRBs (Advarra and WCG IRB) for review and approval of all study protocols, specific study documentation, and study participant facing information. Both Advarra and WCG IRB are organized and operates in compliance with: FDA, OHRP, and International Conference on Harmonization (ICH).
Sanguine operates under an electronic informed consent process which executes 21 CFR part 11 compliant e-signatures, and Sanguine systems interacting with study participant information are HIPAA-compliant.