Flow Cytometry Consulting
For biotech, pharma, academic labs, flow cores, and clinical teams
SuperNova Flow Cytometry provides expert consulting across the entire workflow—from experimental design and panel development to validation, SOP creation, regulatory alignment, and data interpretation. We help teams build robust, reproducible, and scalable flow cytometry workflows tailored for research, clinical, and manufacturing environments.
- Pipeline support from R&D to AD/PD, QC, and Manufacturing
- FDA-aligned validation and qualification strategies for IND and BLA
- ATP development, SOP creation, and assay standardization
- Panel design for conventional and spectral flow cytometry
- Support for RUO, CLIA, cGMP, and IVD environments
Built for Every Flow Cytometry Environment
Biotech & Pharma
Pipeline consulting across R&D, AD, PD, QC, and Manufacturing (ATP, SOPs, Guidance)
Regulatory alignment for IND and BLA submissions
Fit-for-purpose assay validation and qualification strategies
Instrument and reagent selection for scalability
Academia
Experimental design to maximize publishable outcomes
Data analysis support for population identification and interpretation
Flow cytometry rigor for grants and manuscripts
Panel design optimization for complex biological questions
Flow Core Facilities
Standardization of protocols across instruments and users
Training programs for staff and researchers
Workflow optimization to reduce inefficiencies and errors
Support for high-throughput and multi-user environments
Clinical & Translational Labs
CLIA-aligned assay workflows and validation strategies
Alignment of data outputs with clinical endpoints
Support for diagnostic and translational applications
Reproducibility and robustness for regulated environments
End-to-End Flow Cytometry Consulting
End-to-End Flow Cytometry ConsultingFrom experimental design to clinical implementation, SuperNova provides consulting across the full flow cytometry
workflow to ensure scientific rigor, regulatory alignment, and operational efficiency.
- Bridge gaps between Discovery, Translational, and Manufacturing teams
- Ensure assay continuity across environments (RUO → GMP → Clinical)
- Reduce delays and costly rework during scale-up
- Align workflows for efficient technology transfer
- High-dimensional and conventional panel design
- Fluorochrome selection and spillover optimization
- Controls strategy (FMO, biological, instrument)
- Assay robustness and reproducibility
- Develop validation plans aligned with FDA expectations
- Support IND and BLA submission readiness
- CLIA and cGMP-aligned assay strategies
- Fit-for-purpose validation based on intended use
- Analytical Target Profile (ATP) development
- SOP creation for sample prep, staining, and acquisition
- Standardized workflows for data analysis
- Designed for RUO, CLIA, cGMP, and IVD environments
- Platform selection (conventional vs spectral)
- Vendor-agnostic recommendations
- Reagent optimization and cost-efficiency
- Scalable solutions for growing programs
- Customized training programs for teams and core facilities
- Gating strategy development and troubleshooting
- High-dimensional data analysis support
- Translating data into biological and clinical insights
- Evaluate team expertise and gaps
- Customized training programs
- On-site and virtual options
- SCYM-aligned competency development
Expertise You Can Trust
SuperNova Flow Cytometry brings deep expertise across academia, biotech, and clinical environments to deliver consulting that is scientifically rigorous, operationally practical, and aligned with regulatory expectations.
- Experience across academia, biotech, and clinical laboratories
- Proven expertise in cell and gene therapy workflows
- Deep understanding of FDA, IND, BLA, CLIA, and cGMP expectations
- Focus on reproducibility, robustness, and scalability
- Bridging scientific rigor with real-world operational execution
Led by Industry & Academic Expertise
Dr. Christian Aguilera-Sandoval is an expert in immunology and flow cytometry with experience spanning academia, biotech, and translational research.
• NIH-funded research and contributions to cell and gene therapy development
• Experience training scientists across academia, core facilities, and industry
• Former immunology instructor at UCLA and UNC-Chapel Hill
• White House, California Senate and California State Assembly recognition for teaching excellence
• Proven experience translating flow cytometry into research and clinical impact
Trusted by scientists, core facilities, and biotech teams across research and clinical environments
Trusted by scientists, core facilities, and biotech teams across research and clinical environments
Simple, Efficient, Impact-Driven
Our consulting process is designed to quickly understand your needs, deliver
tailored solutions, and ensure long-term success.
Free 30-Min Consultation
Discuss your goals, current challenges, and timeline to determine how we can best support your program.
Custom Proposal
Receive a tailored scope of work with defined deliverables, timelines, and transparent pricing.
Execution & Collaboration
Work directly with your team to implement solutions, optimize workflows, and address technical challenges.
Implementation & Training
Ensure long-term success with validated workflows, SOPs, and team training aligned with your environment.
Ready to Optimize Your Flow Cytometry Workflow?
Whether you’re developing a therapy, running a core facility, or preparing your next publication
SuperNova Flow Cytometry helps you get it right the first time.
No obligation. No pressure. Just expert guidance tailored to your needs.