How we work
Tell us about your research goal, candidate or model needs. We work with you to design the study, run the experiments and interpret 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.
Work with our scientists to select models and assays for candidate comparison, efficacy, safety, mechanism or tumor–immune studies. Deliverables include a defined package of data, images and a study report.
Helpful information to shareProject goal, candidate details, available samples and intended deliverables
Discuss a contract study ↗We confirm available models, culture products, technical documentation and delivery requirements for your study, with technical support or contract research available when needed.
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.
You share the research objective, candidate or model needs, along with any available samples or data; our scientists then discuss suitable models, assays and study options with you.
Together, you and our team define the study design, controls, deliverables, milestones and cost, then confirm confidentiality, material transfer and kickoff requirements.
We provide model updates and interim results at planned milestones and review any required adjustments with you.
You receive the agreed data, images, analyses and report, then review the findings with our team and plan the next study or development step.
Global project coordination
Nanjing leads core R&D and primary laboratory execution. Shanghai works with clients and partners in China, while Philadelphia supports scientific discussion and cross-regional coordination for international clients. The kickoff plan clearly sets out the laboratory location, contracting entity, material flow and delivery arrangements for smooth cross-regional execution.
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 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 explain the current findings and discuss the options with you: continue culture, add material, adjust the study scope or bring the current stage to a close. We agree on the next step together 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.
During quotation, we assess the product, batch, destination, storage conditions and applicable requirements, then provide the appropriate international supply and shipping plan.
Share your objective and any available samples or data. Even an early idea is enough to begin.
How we work
Tell us about your research goal, candidate or model needs. We work with you to design the study, run the experiments and interpret 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.
Work with our scientists to select models and assays for candidate comparison, efficacy, safety, mechanism or tumor–immune studies. Deliverables include a defined package of data, images and a study report.
Helpful information to shareProject goal, candidate details, available samples and intended deliverables
Discuss a contract study ↗We confirm available models, culture products, technical documentation and delivery requirements for your study, with technical support or contract research available when needed.
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.
You share the research objective, candidate or model needs, along with any available samples or data; our scientists then discuss suitable models, assays and study options with you.
Together, you and our team define the study design, controls, deliverables, milestones and cost, then confirm confidentiality, material transfer and kickoff requirements.
We provide model updates and interim results at planned milestones and review any required adjustments with you.
You receive the agreed data, images, analyses and report, then review the findings with our team and plan the next study or development step.
Global project coordination
Nanjing leads core R&D and primary laboratory execution. Shanghai works with clients and partners in China, while Philadelphia supports scientific discussion and cross-regional coordination for international clients. The kickoff plan clearly sets out the laboratory location, contracting entity, material flow and delivery arrangements for smooth cross-regional execution.
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 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 explain the current findings and discuss the options with you: continue culture, add material, adjust the study scope or bring the current stage to a close. We agree on the next step together 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.
During quotation, we assess the product, batch, destination, storage conditions and applicable requirements, then provide the appropriate international supply and shipping plan.
Share your objective and any available samples or data. Even an early idea is enough to begin.
