SOC 2 Type I
PlannedEvidence collection begins in the month after Syncanix launches commercially.
- Target:
- Q3 2026
- Evidence:
- Vanta
Concrete targets per framework, not aspirational adjectives. Out-of-scope frameworks are explicit so procurement readers know upfront. Material changes ship via PR review and trigger a rebuild on merge.
Last updated: . Questions: admin@syncanix.com.
Evidence collection begins in the month after Syncanix launches commercially.
Continuous-monitoring window opens with Type I; report targeted ~9 months post-launch.
70-80% control overlap with SOC 2; evidence collected concurrently.
AI-disclosure copy + persistent chat-header indicator translated into the 6 launch languages; review by EU privacy counsel pending pre-launch sign-off.
DPA template + SCCs Module Two + UK ICO IDTA addendum + Swiss FADP rider. Reviewed by EU privacy counsel before each release.
Implemented to a GDPR + CCPA superset that maps to the 19 US state-level laws in force as of 2026-05.
Not supported in v1. No BAA available. AUP explicitly prohibits PHI. BAA + HIPAA-eligible AWS services planned for v2 if a healthcare deal materialises.
Authorisation path is 18+ months and ~$500k. Deferred indefinitely; revisit when a federal procurement opportunity justifies.