All functions
Every function's documents. One OS underneath.
Different documents, different sources of truth, different deadlines. So each function gets its own application, built for how that team actually works.
The lifecycle
The same work repeats at every stage.
From discovery to post-market, the underlying work never changes: synthesizing fragmented source data into compliant, defensible narratives, then reviewing them line by line. That synthesis and review is the manual, expensive, error-prone part of every phase. That is the work SyncIQ takes on.
Discovery through registration.
- IND, IMPD and CTA packages
- Protocols
- Investigator brochures
- Clinical study reports
- First Module 2 and 3 summaries
Functions
Five functions, each with the applications that serve it.
Regulatory Affairs
01Dossier authoring, label changes, guidance answers
Submissions authored and reviewed, from your own records.
Regulatory Atlas · Label Watch · RegIntel · Vault
Explore Regulatory Affairs
Clinical Development
02CSRs, protocols, investigator brochures
Clinical study reports from study data, protocols from one source.
Clinical Scribe · Protocol Studio
Explore Clinical Development
Market Access
03Formulary position, value dossiers, payer evidence
Value dossiers per market, formulary position per payer.
Formulary Verification · Value Dossier
Explore Market Access
Quality & Manufacturing
04Deviations, CAPAs, APQRs, SOPs
Deviation investigations written from the records they cite.
Investigation Desk · APQR Engine · SOP Studio
Explore Quality & Manufacturing
Pharmacovigilance
05PBRERs, PSURs, narratives, signal evaluation
Safety writing, from PBRERs to signal evaluations.
Aggregate Safety · Signal Desk
Explore Pharmacovigilance
Regulated document work outside these? Financial services → Or tell us what you're solving →
Start where it hurts.
Pick the function slowing your team down today. We'll run it live on a section of your own work.
Request a demoYour data stays in your environment. Customer data never trains foundation models.