Researchers

Human Saliva Samples

Access human saliva samples from difficult-to-reach or rare patient populations,
including event-based or longitudinal collection.

Saliva Specimen Collection

With Sanguine, you get access to a nationwide reach of patient communities and unparalleled biospecimen collection capabilities to obtain human saliva samples for a diverse range of translational disease research needs.

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.

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.

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Longitudinal and event-based biospecimen and data collection

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Same-day sample collection and delivery

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Nationwide patient member community to meet complex inclusion/exclusion criteria

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Medical record-verified eligibility and pre-screening

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Access to electronic medical records, health histories, patient-reported datasets

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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.

Genetic

Genetic

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Neurodegenerative & Neuropsychological

icons-70-x-70-hematological

Hematologic

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Oncology

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Metabolic

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Infectious Disease

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Autoimmune & Inflammatory

cardiovascular

Cardiovascular

Genetic

Genetic

icons-70-x-70-neurodegenerative

Neurodegenerative & Neuropsychological

icons-70-x-70-hematological

Hematologic

icons-70-x-70-oncology

Oncology

icons-70-x-70-metabolic

Metabolic

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Infectious Disease

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Autoimmune & Inflammatory

cardiovascular

Cardiovascular

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.

Others Services

Longitudinal & Event-Based Collection

Patient Surveys & Questionnaires

Onsite & Same-Day Healthy Control Programs