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Finepoint Science
SIMS for Scientific Work
A new kind of scientific workspace.
SIMS is one workspace for the whole scientific effort: explore with AI, build the evidence, draft and review documents, and work with partners. Everything that happens lands on the record, ready for the next reviewer, sponsor, or audit.
Pharma-Biotech Lifecycle
Four workspaces that match how the industry actually runs, so discovery work flows into studies, batches, and release without re-entry.
AI Discovery
Explore candidates and draft with AI while every source and decision stays on the record.
Clinical Research
Run studies where protocols, specimens, and sponsor reviews live in one governed place.
Manufacturing
Move batch records and release documents through review with full version history.
Quality Control
Tie testing, COAs, and stability data to the batches and studies they certify.
Why Choose SIMS
Generic AI tools forget where claims came from. SIMS never does.
Built by a Licensed Lab
SIMS comes from a Health Canada–licensed (DEL · CDS) lab that lives with cGMP every day — not from a generic SaaS playbook.
AI Inside the Workflow
Draft, compare, and summarize where the evidence lives, so review starts instead of starting over.
Traceable by Default
Sources, edits, approvals, and exports stay inspectable. When the question is "why did we conclude this?", the answer is one click away.
Grows With You
Start as a three-person lab in the cloud beta; scale to subsidiaries and external partners on the same platform.
From Draft to Durable Record
The same path every time: draft with AI, attach evidence, review, sign, export.
Draft With AI
Start from a template or a prompt. The draft lands in the project, not in a chat window.
Attach the Evidence
Link sources, lab results, and prior decisions to the claims they support.
Review and Sign
Reviewers comment, request changes, and sign off, with every action logged.
Export and Defend
Send the signed record out with its full history attached, ready for any audit.
Lab evidence, when the work needs it.
Finepoint Labs is our Health Canada–licensed analytical lab, running potency, stability, and method validation programs with 24–48h rush turnaround available.
Explore LabsPotency Testing
Quantification of APIs, cannabinoids, and controlled substances with validated HPLC, GC, and LC-MS/MS methods.
Stability Studies
Long-term and accelerated stability programs for shelf-life, degradation, and storage-condition decisions.
Method Validation
Method development and validation that stands up to regulatory review, for new matrices, compounds, and workflows.
From first draft to signed record.
Start in the SIMS cloud beta today, free and with no setup. When you need on-premise deployment, sponsor access, or QC integration, Finepoint builds it with you.
Evidence-Linked Drafts
Every claim in a draft can point to the source it came from.
Signoff That Sticks
Reviews, approvals, and signatures stay attached to the record, version by version.
Partner Access, Scoped
Sponsors and CROs see exactly their work. The audit log sees everything.
A Real Lab Behind It
Built by a Health Canada–licensed lab. 24–48h rush testing available through Finepoint Labs.