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Turn every regulatory signal into a closed-loop action.
Orthic helps Indian pharmaceutical QA teams connect regulatory findings, corrective actions and supporting evidence. Start with an agreed workflow at one facility.
§1
Signal → CAPA in one click
Review available regulatory notices with source context and portfolio matches. Start a CAPA draft for your QA team to evaluate.
§2
Tamper-evident audit entries
Check the integrity of recorded audit entries and export an inspection preparation summary.
§3
MLR AI analysis engine
Draft CAPAs, review SOPs, assess ALCOA+ gaps, and prepare DDRS migration checklists — AI drafts, you approve.
1 facility
Start with an agreed QA workflow
QA-owned
Your team reviews actions and evidence
₹1.2L
Starter software subscription per year
Before you get started
Orthic is provisioned for you by your firm, as part of their use of Orthic's compliance platform. Before you continue, please review how Orthic handles your data.
Orthic stores your account details, and the compliance data your firm enters (signals, CAPAs, evidence, audit trail) — see the Privacy Policy for the full list and why each is collected.
Your audit trail is append-only and cannot be deleted, including by Orthic, once written — the same guarantee that makes it credible to a regulator. See Privacy Policy §7 before you rely on it.
You can request a full export of your data at any time — Settings → Export Everything.
Questions about your data go to [grievance officer contact — FILL IN once designated].
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Legal & Regulatory AdvisoryADVISORY
Read-only posture across legal & regulatory procedures. Orthic flags — it does not act.