# DenQAI: first 90 days continuity plan

File-specific companion · 2026-09-10

## Purpose

What must remain stable during the first 90 days of an ownership or operating transition?

**Who:** Transition owner, clinical lead, operations manager, and workstream reviewers

**Records:** Aggregate patient handoff; role/access coverage; payer status; cash controls; evidence and milestones for the transition.

## Complete the file

1. Use the phase and workstream rows to identify the control needed in each transition window.
2. Answer owner_question with required_aggregate_evidence, accountable_owner, and target_window.
3. Record patient_or_staff_effect, break_condition, status, and the next corrective action.

## Definitions

- **Continuity control:** Specific process intended to keep necessary care and operations functioning.
- **Target window:** Defined transition period for completing the control.
- **Patient or staff effect:** Observable consequence of the control or its failure.

## Fictional example

Fictional example: In Days 0–30, the team-continuity row identifies no backup for payment posting; assign access, training, and evidence of coverage.

## Review and next action

Close day-one access and continuity gaps before introducing later process changes.

This raw transition plan does not establish clinical appropriateness or prove readiness merely because the target date is filled.

[Related DenQAI guide](https://denqai.com/operations)

## AI coach prompt

Help me use DenQAI’s first 90 days continuity plan. My question is: What must remain stable during the first 90 days of an ownership or operating transition? Explain these terms in plain language: Continuity control, Target window, Patient or staff effect. Ask one question at a time about the required records: Aggregate patient handoff; role/access coverage; payer status; cash controls; evidence and milestones for the transition. Walk through the supplied fictional example before asking me for inputs. Treat every missing value as unknown, not zero. Do not invent source records, contract terms, legal conclusions, or clinical facts. Use only permitted fictional or aggregate, non-identifying information. Follow this boundary: This raw transition plan does not establish clinical appropriateness or prove readiness merely because the target date is filled. End with the missing evidence and this next step: Close day-one access and continuity gaps before introducing later process changes.

## AI review prompt

Review my permitted fictional or aggregate draft of DenQAI’s first 90 days continuity plan against the file instructions. Check each required field and period, units, evidence locator, assumptions, arithmetic where formulas are actually supplied, and unresolved contradictions. Check the sequence: Use the phase and workstream rows to identify the control needed in each transition window. Answer owner_question with required_aggregate_evidence, accountable_owner, and target_window. Record patient_or_staff_effect, break_condition, status, and the next corrective action. Separate facts from assumptions and missing records. Do not supply unsupported numbers or make a professional decision for me. Apply this limitation: This raw transition plan does not establish clinical appropriateness or prove readiness merely because the target date is filled. Return corrections, questions for the responsible reviewer, and the next action.