Focused quality, CAPA, or regulatory workflow
€15,000 - €30,000
To understand the current setup, set priorities, and avoid restarting a vague project.
- Review of the current setup and blockers
- Priorities and work scope clarified
- Technical or product decisions documented
- The level of validation, evidence, audit trail, and role separation that must hold cleanly
- The integrations with DMS, QMS, ERP, signature, directory, LIMS, or existing document repositories
- The need for continuity, recovery, maintenance, and audit readability in a tightly controlled environment
In a pharma context, budget mostly rises with the level of evidence, traceability, and separation of duties required by the workflow.






