Researchers

Employer Onsite Collection
Programs

Research Biospecimens On-Demand

Processing and measurement delays after biospecimen collection can negatively impact research results. With a Sanguine-managed onsite donation program at your research facility or office complex, you can obtain fresh specimens from your colleagues within minutes of collection. Onsite programs enable employees at all seniority levels to participate in your organization’s R&D as blood or other biospecimen donors.

Read the blog or watch the webinar on-demand to learn how researchers use our Onsite Collection Program

Convenient

  • Streamlined, easy access to healthy samples
  • Samples ready for pickup immediately after collection
  • Enable the best science with fast, fresh specimens

Experienced Provider

  • Informed consent, IRB, and regulatory compliance managed on your behalf
  • Employee privacy protected through HIPAA compliance
  • Program setup within 8 weeks of contract

Flexible & Customizable

  • Specify inclusion/ exclusion criteria
  • Support team manages logistics and requests
  • Accommodate specimen collection-specific requirements and changes        

Blood Donor Programs in Action

>90%

Fulfillment Rate

200+

Healthy Participant
Studies Completed

700+

Onsite Employee
Participants

18

Organizations with Onsite Programs

135+

Same-Day Studies
Completed

1

Convenient

2

Quick Turnaround Time

3

Customizable

4

Longitudinal Sampling

maximize sample viability

Maximize Sample Viability

Match control for demographic variables

Match Control for
Demographic Variables

One Partner for Biospecimen Procurement

   Explore our service offerings to cut timelines and costs, reduce variability, and translate your data into insights.

 

Disease State & Healthy Leukopaks
Human PBMCs
Human Serum and Plasma
Biorepository Services
Longitudinal Sampling & Event-Based Collection
Lymphocyte Isolation
Noninvasive Skin Tapes
PBMCs Isolation Services for Clinical Trials
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

icons-70-x-70-infectious-disease

Infectious Disease

icons-70-x-70-auto-immune-inflammatory

Autoimmune & Inflammatory

cardiovascular

Cardiovascular

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.

 Get started with the program