Pharma & generics
The portfolio never stops moving.
Variations, renewals, new markets. Every registration has its own clock, and the team that keeps them current is the same team drafting the next submission.
SyncIQ authors from your own records, expands one approved dossier into every market, and drafts the lifecycle work from the change record, before the date moves.
Data secure in your cloud21 CFR Part 11-awareSOC 2 Type II (in progress)ISO 27001 (in progress)Your data never trains foundation modelsTrust and security →
Where teams like yours start.
Regulatory Affairs
Dossier authoring, label changes, guidance answers. Four applications live.
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Clinical Development
CSRs and nonclinical study reports from study data.
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Market Access
Formulary position reconciled against your contracts.
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Quality & Manufacturing
Deviations, CAPAs, APQRs and the documentation an audit asks for.
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Start where it hurts.
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.