Projects and new product introduction
Projects & NPI
Coordinate projects and new product introduction (NPI) across departments. Give each action an owner and a date, follow milestones and identify the work or decisions holding a project up.
For project leads and cross-functional teams introducing products or delivering operational changes.
What you can manage
Project plans
Set the stages, target dates and workstreams for each project, from initial scope to operational handover.
Reusable project structures
Save a repeatable set of stages and workstreams as a template. Reuse that structure for the next product or project, then add its own actions and dates.
Actions and responsibilities
Assign work to named people and track status, priority, due dates and supporting document links.
Dependencies and blockers
Show when an action depends on other work. Record the issues and decisions that prevent progress.
Milestones and timelines
See important project dates and upcoming milestones across your portfolio.
Project reporting
Review overdue actions, blocked work and project health. Identify projects that need attention or an updated status.
Explore the dashboard
Select a priority to open the relevant project actions, then open an action for its dependency and next step.
Consinova Projects & NPIExample dataProject overview
Project health, overdue actions and decisions.
Overdue actions
| Record / work | Owner | Date | Status | Open record |
|---|---|---|---|---|
| Technical lead | 26 Oct 2026 | Overdue | ||
| Quality lead | 28 Oct 2026 | Decision needed | ||
| Engineering lead | 05 Nov 2026 | Blocked | ||
| Project lead | 09 Nov 2026 | Upcoming | ||
| Operations lead | 16 Nov 2026 | Upcoming |
Example records in a website demonstration based on the system dashboard.
Configuration, tailoring and bundles
Discuss the records, roles, workflows and reports your organisation needs. This system can be included in a quote with any of the other Consinova systems.
Discuss this system or a bundleValidation
Annex 11 and Annex 15
Consinova systems can be validated in compliance with EU GMP Annex 11 and Annex 15 for their intended use.
Validation is specific to the configured system, the way your organisation uses it and the procedures that support it. The scope, risk assessment, testing, evidence and responsibilities are agreed for your implementation.
Include validation in your enquiry EU GMP guidance: Annex 11 — Computerised Systems; Annex 15 — Qualification and Validation ↗
