01
Pick the pilot objective
One high-impact workflow — document control, CAPA, or audits — with a small cross-functional team and clear acceptance criteria.
Before day one
30-Day Pilot Program
Start Your 30-Day Quality Pilot
A structured 30-day engagement built around one high-value workflow — document control, CAPA, or audits. You define success, we configure the environment, and together we prove fit before any broader commitment. Pilot records carry the same ALCOA+ data integrity expectations as production use.
- Tell us which workflows matter most right now.
- Share your current tools and rollout priorities.
- Ask about pilot scope, validation, or compliance questions.
Want to see the platform first? Request a demo instead.
How the 30 days run
One workflow, one team, 30 days — success metrics defined before day one, documented qualification evidence at the end.
02
Configure & validate
We configure the workflow, roles, and templates in a validated, controlled environment.
Controlled setup03
Run & measure
Your team works real records in the live workflow and measures against the agreed success metrics.
Real records04
Review & decide
Results against acceptance criteria, with a defined expansion path for after go-live — or a clean stop.
Go / no-go
You leave the pilot with:
Configured workflow
Trained users
Documented qualification evidence
A clear go / no-go decision
Why Choose Complere
Built for regulated life-sciences teams that need control, auditability, and practical adoption.
Scope
Choose one workflow to improve first
Document control, CAPA, audit follow-up, or another high-value process.
Success
Define measurable pilot outcomes
Cycle time, visibility, retrieval, and adoption metrics make the first phase concrete.
Expansion
Plan what comes next
A good pilot naturally tees up broader module or site rollout.
Want to see the platform before committing to a pilot?
Request a 45-minute demo and we will show you the exact workflows and compliance controls relevant to your team.