Expertise in Extracellular Vesicles, Nanoparticles, Nanobubbles & VLPs
Our consulting services help researchers and organizations accelerate discovery, streamline analytics, and scale production for biological and synthetic nanoparticles.
Who We Support
Academic and translational research labs
Biotech and biopharma companies
CROs and CDMOs working with EVs, LNPs, nanobubbles, viruses, or virus-like particles
Core Areas
Workflow Design & Feasibility
Optimize isolation, purification, and characterization workflows for EVs, nanobubbles, and VLPs. Identify process gaps and analytical bottlenecks.
Process Development & Scale-Up
Transition from bench to pilot and GMP scale with guidance on reproducibility, yield, and quality control.
Characterization & Analytical Strategy
Develop integrated multi-modal analytics using NTA, flow cytometry, and microscopy to quantify size, concentration, and particle integrity.
Regulatory & Quality Readiness
Align your workflows with cGMP and regulatory expectations for particle-based therapeutics and diagnostics.
Commercialization & Partnership Strategy
Bridge the gap between R&D and scalable operations through partnership, outsourcing, and technology integration strategies.