Develop the research
Explore sources and approaches with AI. Prepare protocols, experiment records, and study reports with scientific review built into the work.
SUPPORT FOR SCIENTIFIC PROGRAMS
The infrastructure behind psychedelic research.
Finepoint brings scientific expertise, laboratory experience, and SIMS together to help drug-development teams move their work forward. Explore questions with AI, coordinate studies, and keep the records and decisions connected.
SUPPLY AND LABORATORY WORK
Build the program around the work it needs.
We work with drug-development teams and scientific partners to define the materials, testing, documentation, and expertise their program calls for. Supply and laboratory work are the focus of our current offer.
Laboratory support for your next decision.
Bring the research question and the material you need to understand. We can help plan the analytical work, establish suitable methods, and interpret the results with your team.
- Analytical testing and material characterization
- Method development and validation
- Stability studies and scientific review
Controlled-substances licence holder: CCrest Laboratories Inc. The licensed activities and Special Access Program supply experience described on this page relate to the licence holder named here.
SPECIAL ACCESS EXPERIENCE
Experience with the responsibilities of supply.
The licence holder has supplied MDMA to physicians treating patients with post-traumatic stress disorder (PTSD) through Health Canada’s Special Access Program (SAP), outside clinical trials.
These supplies were made under specific authorizations. Special Access Program authorization is distinct from market approval for a drug.
AN ILLUSTRATIVE PROGRAM
From a research question to the next decision.
In this fictional example, a team is preparing an early-stage compound characterization study. A configured SIMS workflow could keep the protocol, laboratory work, review, and follow-up connected.
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Define the study
Agree on the question, sample requirements, analytical methods, and responsibilities before work begins.
- Record
- P-014 · Research protocol
- Responsible role
- Program lead
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Coordinate laboratory work
Confirm the authorized scope, plan material handoffs, and record the laboratory work and results.
- Record
- P-014 · Material and testing record
- Responsible role
- Laboratory lead
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Review the findings
Check the results against the study plan, resolve questions, and record the review and approval.
- Record
- P-014 · Scientific review
- Responsible role
- Scientific reviewer
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Assign the next steps
Document the decision and assign any additional testing or information requests, with owners and due dates.
- Record
- P-014 · Follow-up tasks
- Responsible role
- Program coordinator
SIMS FOR RESEARCH TEAMS
Keep the science and the work around it connected.
A program produces questions, protocols, calculations, results, and decisions. SIMS gives the team a shared place to develop that work with AI, coordinate responsibilities, and review what comes next.
Run the process
Configure forms, formulas, and process stages around the study. Record the data and keep the method and version used with each executed record.
Coordinate the team
Organize workspaces, assign tasks, and track due dates. Give colleagues and external collaborators access suited to their role.
Review and sign
Bring the findings to the people responsible for review. Keep electronic signatures, changes, and decisions with the work they refer to.
SAFETY INFORMATION AND FOLLOW-UP
Supporting pharmacovigilance teams
Safety follow-up depends on clear information and clear responsibilities. We can help configure SIMS so staff can record incoming reports, assign information requests, track follow-up, and document internal review.
The workflow is configured around the team’s operational responsibilities, with human review. Medical assessment and regulatory reporting remain with the responsible professionals and their established systems.
Staff record an incoming report
A coordinator assigns follow-up
Designated reviewers assess the information
The team documents the decision and next steps
Take on more without building every capability in-house.
Bring together supply, laboratory expertise, and software around your program. Finepoint helps define the work and coordinate the support, so a small team can spend more time on the science and less time managing handoffs.
SUPPORT FOR SCIENTIFIC PROGRAMS
Discuss a scientific program Tell us about the program you want to advance.
Share the scientific question, the stage of your work, and the support you need. We can discuss the scope, laboratory requirements, and how SIMS could fit your team.