Diagnostics Companies
Prospective and retrospective research collection programs shaped around assay-development needs.

Research collection, built to specification
We help sponsors, diagnostics companies, biotech and pharma teams, CROs, and academic partners turn defined research needs into coordinated collection programs.
Recruitment & collection feasibility
Explore current disease-area populations and start a conversation about what your research program needs collected.
Unique participants & prospects
In the current consolidated network. Disease-area records may overlap and should not be added together to calculate unique people.
Selected research area
A substantial respiratory research population for sponsors exploring asthma-focused recruitment and prospective collection feasibility.
Potential research & collection opportunities
These are feasibility opportunities, not confirmed specimen availability or guaranteed eligible donors. Collection feasibility is confirmed project-by-project.
Disease-area counts reflect participant/prospect records and may overlap across research areas; they do not sum to the 1,400–1,500 unique people in the consolidated network. Counts are shown as approximate ranges rounded to the nearest hundred to protect participant privacy. Counts indicate recruitment and collection feasibility populations, not guaranteed eligible donors.
Related research experience
These programs have no matching participant-network category or count. A study record does not establish a participant cohort or enrollment.
Available inventory
Partner-reported lung oncology, normal/adjacent control tissue, and oncology FFPE categories. Quantities and QC confirmed during quotation; research use only.
Clinical research programs
Requirement-led
We begin with the exact collection need—not a predetermined menu.
Geography-aware
Participant, site, and delivery considerations are addressed in the operating plan.
Documentation-minded
Study details remain connected through collection and client-directed delivery.
Capabilities
From participant identification through client-directed delivery, each element is shaped around the study—not forced into an off-the-shelf process.
Study-specific collection programs aligned to your protocol, population, and timeline.
Explore 02Focused outreach and participant coordination for defined study criteria.
Explore 03The requested context, organized around each collection event.
Explore 04Clear, traceable documentation shaped to study requirements.
Explore 05Defined preparation and client-directed delivery workflows.
Explore 06An operational model built around the specimen, cohort, geography, and data you need.
ExploreA clear path from need to delivery
We assess the indication, specimen requirements, cohort, data needs, geography, and schedule.
Your requirements become a practical collection workflow with defined milestones and responsibilities.
Potential participants are identified and coordinated against the study’s defined requirements.
Collection events are scheduled and conducted according to the agreed research workflow.
Requested preparation and documentation steps are completed according to client direction.
Materials are coordinated for delivery to the client-designated destination and schedule.
Our network
Spectrum Clinical Research Labs works alongside established organizations across biospecimen research, diagnostics, and clinical research services to expand the reach and flexibility of our collection programs.
Industry Collaborator
Industry Collaborator
Industry Collaborator
Who we support
We collaborate with organizations seeking a responsive research collection partner and a clear operating path.
Prospective and retrospective research collection programs shaped around assay-development needs.
Targeted biospecimen and clinical-data coordination for discovery and development programs.
An operational collection partner that can work within study-specific requirements and timelines.
Purpose-built collection support for investigator-led and collaborative research programs.
Start a conversation
Share the indication, specimen type, cohort, geography, and timeline. We’ll start with the right questions.