Clinical
Benchmarks’ USDA clinical and FDA pre-clinical expertise is focused on licensing our client’s products or maintaining/clarifying existing product life cycles. Necessary facilities are in place to house surrogate models for small target or laboratory species in-house. Larger surrogate or target species are managed by our personnel at off-site locations. Inspected and certified by Animal Welfare, all studies conducted onsite are IACUC approved.
Benchmark’s Clinical Services include:
Please contact us if a service is not listed, as it may be available
- Proof of Concept
- Immunogenicity
- Safety and Challenge
- Hyperimmunization for Antibody Production
- Tissue and Immune-Cell Isolation.
- Animal Model Development (Target or Surrogate)
- Sample collection, processing, and storage (performed onsite or shipped directly to client)
- Withdrawal Studies
- Product Development
- Novel Sampling Methods and Analytic Testing
- Reduction
- Refinement
- Replacement
- Novel Sampling Methods and Analytic Testing
- Serum- and Antibody-Response Assays
- Efficacy/Immunogenicity (i.e. Minimum Immunizing Dose)
- Specialized Reagent Production
- Interference
- Vaccine Safety (Target and Surrogate Animal)
- Field Safety
- Data Capture
- Flow Cytometry
- CMI Bioassays
- PCR Cytokine Cascades
- Innate-Response Assays
- Mucosal-Response Assays