01
Collect the study record
Bring together the approved template, protocol, SOP context, LIMS output, tables, and instrument files.
Provide an entire study.
Get a drafted report.
ScienceMachine's AI reliably drafts regulatory and client reports within existing report templates, allowing you to deliver up to 80% faster.
Preparing
Table of contents
Page 1 of 126
Results
126 pages to assemble
Scanning page 1
Sources connected
Sections populated
Checks applied
A controlled workflow with a scientist in command.
02
Populate the report
Build the table of contents, insert data and chromatograms, and draft sections according to the controlled workflow.
03
Review, QC, and sign
Use tracked changes, run an independent QC workflow, capture electronic approval, and export the final record.
Up to 80% faster drafting, making it more tailored to each client.
We configure the workflow around your systems, source formats, decision rules, and approval model—then validate the version your team will use.
Your existing format
Preserve client-specific Word templates, study structures, terminology, and presentation rather than adopting a generic output.
Multi-source population
Structure content from LIMS, spreadsheets, RTF files, SharePoint folders, protocols, and study data.
Independent QC
Pass the generated draft through a separate, approved Document QC workflow before final review.
Complete record
Retain versions, code traces, source links, edits, signatures, and exportable audit logs with the report.
Generate reports in the formats your clients need.
Microsoft Word
Microsoft Excel
HTML
Microsoft PowerPoint
Results proven by industry leaders
“We worked with ScienceMachine at Inoviv and had a great experience. They helped us reduce the time we were spending on QC and reporting by 80%, allowing us to meaningfully increase our capacity.”
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