Our team supports investigators from first study steps to biospecimen metadata tracking, storage and sample life-cycle, improving scientific rigor, and reproducibility.
Areas of Consultation
Before Submitting Your Study
Get input on study design, IRB considerations, and pre-analytical factors
- Study Design & Protocol Development
- Informed consent language considerations
- Pre-analytical variables
- Regulatory & Compliance Guidance
Request consultation at this stage
When Setting Up Operations
Assistance with workflows, data management, and cost estimation
- Biospecimen Processing & Storage
- Data Management & LIMS integration
- Specimen Collection Planning
- Cost Estimation
During Collection Processing
Guidance on retention strategies and readiness for analysis
- Long-Term Storage
- Readiness for Analysis
- Metadata Tracking
