Care that stands up to scrutiny.
Back to HomeThis page is maintained by Ranovexa to summarise our current clinical, regulatory and data-protection practices. It is not an independent certification.
Every clinical protocol is authored, reviewed and signed off by our internal Clinical Board.
ID verification, background checks, credential verification and annual re-verification for every caregiver.
Segregation at source and pickups via CPCB-authorised waste operators in each city.
Devices are inspected before every deployment. Preventive maintenance is scheduled per manufacturer specification.
Health records are stored with role-based access, audit logs and encrypted at rest. Access is logged.
All complaints are triaged within 4 hours and closed within 24 hours, with escalation to the Clinical Board.
Reporting a concern
Compliance concerns can be reported to compliance@ranovexa.com. Reports are reviewed by an officer independent of the operational team.