How we work
Start with your research goal. Together we define the model and assays, run the study and deliver the results.
Project team
A scientific lead works with you on model and endpoint selection. A project lead coordinates laboratory execution, data review and the final report.
WAYS TO WORK TOGETHER
Begin with contract research, model and product supply, custom development or scientific collaboration—and combine approaches as the program evolves.
Compare candidates through efficacy, safety, mechanism or tumor–immune studies with our scientists. Receive the agreed images, data, analysis and study report.
Helpful information to shareProject goal, candidate details, available samples and intended deliverables
Discuss a contract study ↗We help you source models, culture products and technical documentation, with optional technical support or contract research.
Helpful information to shareModel or product name, catalog number or family code, intended use, study scale and delivery region
Request model supply or product details ↗We build and validate a model or assay for specialized tissues, samples, co-cultures or functional endpoints, then plan its follow-on application with you.
Helpful information to shareTarget model, available samples or materials, primary study endpoint and intended follow-on use
Discuss custom development ↗Collaborate on disease models, method development, research programs or joint validation, with study roles, data use and intended outputs agreed at the outset.
Helpful information to shareScientific question, relevant methods or data, proposed roles and intended outcomes
Discuss a scientific collaboration ↗Collaboration process
At each stage, you receive a defined output: study scope, kickoff plan, milestone data and final report.
Share your research goal, candidate and available samples or data. Our scientists will recommend models, assays and study options.
Agree on your study design, controls, deliverables, timeline and cost, then arrange confidentiality, material transfer and project kickoff.
We provide model updates and interim results at planned milestones and review any required adjustments with you.
Review the images, data and report with our scientists, then plan the next step for your program.
Global project coordination
Our Nanjing team performs core R&D and laboratory work. Shanghai supports clients in China; Philadelphia supports international project discussions. Before kickoff, we confirm the study location, contracting entity, material handling and delivery responsibilities.
Leads organoid model development, drug screening, functional validation, multimodal assays and primary laboratory execution.
Works with clients in China on project discussion, scientific coordination and translational collaboration, in close coordination with the Nanjing R&D team.
Supports scientific discussion, study design and cross-regional coordination for international clients. Primary laboratory work is led by the Nanjing R&D team.
Project & procurement documents
Read the project discussion guide, or request model, report, product, quality and shipping information to support study planning and procurement.
See what to share in the first discussion and how a study moves into planning and kickoff.
See how projects start ↗Request the 2026 English edition covering the PDO 2.0 / ALI platform, model and assay capabilities, and representative research applications.
Request documents ↗Request a model dossier covering source, identity and functional characterization, available readouts and relevant applications.
Request documents ↗Request a sample report outline showing how data, images and analyses are presented, then agree the report structure and deliverables before work begins.
Request documents ↗Instructions and batch documents for product onboarding, procurement and quality review, with CoA or SDS where applicable.
Request documents ↗Company and quality-system materials for procurement, quality discussion and vendor onboarding.
Request documents ↗Plan storage, transport and handoff for the relevant product or study material.
Request documents ↗FAQ
Yes. Start with the study objective, candidate type and what is already available; the detailed plan can take shape during the initial scientific discussion.
Start with the study objective, modality and a de-identified sample overview. If confidential candidate details are needed, we first agree on confidentiality terms and a suitable transfer channel. Use coded sample references; patient identifiers are not needed in website inquiries.
We prepare a timeline and quote based on the models, samples, candidates, readouts, replicates and deliverables your study needs.
We share the current findings promptly and evaluate the best path with you, including continued culture, additional material or an optimized study scope. We then document the current-stage findings and agree the next step under the study plan.
Typical deliverables include model QC, methods, raw data, images, analysis and a study report; the final deliverables are defined in the plan.
The applicable contract or collaboration agreement sets out intellectual-property ownership, data-use rights and publication arrangements for the selected collaboration model.
The international team supports scientific discussion and cross-regional project coordination. The study plan defines laboratory location, contracting, material logistics and billing arrangements.
Availability and international shipping are confirmed during quotation based on the product, batch, destination, storage conditions and applicable requirements.
Share your objective and any available samples or data. Even an early idea is enough to begin.
