Spend less time assembling data for R&D program decisions.
Trusted by 200+ life science labs





















Supporting 250+ instrument types, more than 1,000 experiments each month, and millions of samples across diagnostics, genomics, biotech, and regulated testing.
Built for translational and clinical-stage biotech teams.
When evidence spans instruments, CROs and internal teams, review preparation grows. Start with one costly assay or partner handoff. Keep the research and analysis tools that work.
Published Customer Outcomes
From assay data to usable evidence.
Less manual reporting and admin
Across a Biotech's connected assay-data workflows.
Lower data-entry error rate
In one workflow connecting scientific data and reporting.
Shorter data processing time
In one scientific data workflow at a Biotech Lab.
Less time creating cross-team requests
Connected wet and dry lab workflows for a synthetic protein and peptide team.
One Digital Brain moves experimental work into program decisions.
Start every program review with evidence ready.
Ask what the program learned.
Draft the next evidence summary.
Bring experiments, partner results and recorded decisions into view.

Research workflows that adapt as your program advances.
Evidence Across Programs & Partners
Connect candidate, sample and experiment records across teams and partners. Keep reviewed results traceable to their data and methods as programs advance.
Assay Data Without Repeated Copying
GLUE maps supported instrument and partner outputs to records. Smart Actions can return agreed calculations with source files and analysis versions for scientific review.
Personalized Research & Review Apps
Jazz provides focused screens for experiment requests, partner intake and evidence review. Apps use shared Scispot data to preserve one research record.
Experts From Mapping to Adoption
Scispot scientists and engineers map and configure workflows, connect tools, test representative data and train users. Measure preparation time and adoption before expanding.
Show us the data work delaying program review.
FAIR data • pipelines • automation
Instruments • ELN/LIMS/SDMS • 200+ connectors
FAIR data • pipelines • automation
Instruments • ELN/LIMS/SDMS • 200+ connectors
Frequently asked questions
Which biotech R&D teams are the strongest fit?
Translational and clinical-stage biotechs preparing program evidence across instruments, teams and CRO/CDMO partners are a strong fit. Discovery teams can use the same foundation. Start where manual preparation, missing sample history or repeated coordination has measurable cost.
Can we keep our ELN, LIMS and specialist analysis tools?
Yes. Scispot can work alongside supported systems or add native apps. Keep specialist analysis tools and link their inputs, versions and outputs to experiments. We scope file/API connections, access and return paths. You retain access to your Scispot data and exports.
How do we start as research needs change?
Our scientists and engineers start with one assay or partner handoff, linking programs, candidates and samples. Configure protocol versions, screens and review steps; test revisions with representative records, train users and track adoption. Subscriptions include software, integrations, expert delivery and unlimited users within agreed workflow and validation scope.
What research analysis can Scispot automate?
Smart Actions can run agreed calculations, with user preview and approval before saving. Scibot searches permitted evidence, compares recorded fields and drafts summaries. External analysis tools can stay connected. Define inputs, methods and review gates. Scientists assess biological meaning and approve decisions.
How do controls change for regulated development?
Match controls to intended use, from source history and versioned methods to formal procedures, electronic approvals and validation where required. Scispot provides configurable permissions, audit trails and review gates. Trust Vault organizes evidence; scientific and Quality owners define requirements, approve validation and retain regulated sign-off.

Keep source files, method versions, calculations and review decisions in controlled records. Scientific and Quality teams define intended use, validation and final approval.
















