Consinova systems
Pharmaceutical software
Five systems for quality, equipment, stock, projects and recorded checks. Available individually or as a bundle, with configuration and tailoring for your organisation.
Quality management
Hybrid QMS
Manage deviations, corrective actions, changes and risk assessments in one quality management system. See who needs to act, what is overdue and which records are waiting for a decision.
Deviations
Record what happened, investigate the cause and track the actions needed to address it.
Corrective and preventive actions
Assign actions to named people, set due dates and review completion against the source quality record.
Change control
Keep proposed changes, their assessments and implementation actions together, from initiation through review.
Risk assessments
Maintain a register of assessments and the actions associated with the risks you identify.
Effectiveness checks
Plan follow-up checks to establish whether the action taken resolved the issue. Record the result before closure.
Oversight and reporting
Review overdue work, critical items, pending decisions and upcoming dates. Use registers and KPI reports to examine the detail.
Explore the dashboard
Select “Overdue work” to see the outstanding actions, then open a record for its owner, due date and next step.
Your dashboard
Outstanding work, upcoming dates and decisions.
Overdue work
| Record / work | Owner | Date | Status | Open record |
|---|---|---|---|---|
| Quality | 27 Oct 2026 | Overdue | ||
| Warehouse | 28 Oct 2026 | Overdue | ||
| Engineering | 02 Nov 2026 | Awaiting review | ||
| Quality | 06 Nov 2026 | Planned | ||
| Production | 04 Nov 2026 | Awaiting decision |
Dashboard structure and work lists based on the system. All records shown are examples.
Equipment, maintenance and calibration
Computerised Maintenance Management System
Manage equipment records and the work needed to keep them current. Plan calibration, maintenance and revalidation, identify overdue checks and keep completed work and supporting documents with each piece of equipment.
Equipment register
Record equipment identity, location, department, classification, supplier and components in one place.
Calibration schedules
Set calibration requirements and intervals. See the last successful check, the next due date and overdue work.
Maintenance and revalidation
Plan recurring or one-off checks, record completed work and retain the history against the equipment.
Faults and repairs
Record an equipment fault and follow the repair through to the work carried out and its outcome.
Documents and components
Keep certificates and other equipment documents with the record. Link components to the equipment they belong to.
Engineering oversight
View overdue checks by activity and department. Open the affected equipment directly from the dashboard.
Explore the dashboard
Select “Overdue calibration”, then open a balance or pressure sensor to see the overdue check and equipment details.
Dashboard
Outstanding work and current priorities.
Overdue calibration
| Record / work | Owner | Date | Status | Open record |
|---|---|---|---|---|
| Calibration team | 22 Oct 2026 | Overdue | ||
| Engineering | 26 Oct 2026 | Overdue | ||
| Validation team | 20 Oct 2026 | Overdue | ||
| Maintenance team | 25 Oct 2026 | Overdue | ||
| Maintenance team | 12 Nov 2026 | Due soon | ||
| Calibration team | 19 Nov 2026 | Due soon |
Dashboard structure and work lists based on the system. All records shown are examples.
Purchasing, goods receipt and stock control
Stock and Procurement
Follow materials from purchasing and receipt through to release and use. See what needs ordering, which purchases need approval and which stock is still waiting for review.
Stock by material and lot
See quantities, storage locations, lot references and expiry dates. Distinguish received stock from stock available for use.
Purchase orders and approvals
Prepare orders, identify the decisions still required and track orders through to receipt.
Goods receipt and QA release
Record delivered materials and review held lots. Keep quarantined or unreleased stock separate from usable stock.
Demand and replenishment
Review material shortages and purchasing requirements before preparing the next order.
Material movements
Record issues and movements so the stock register reflects where materials are and how they have been used.
Manufacturing planning
Review planned jobs, material needs and reservations alongside purchasing and stock availability.
Explore the dashboard
Select “Stock awaiting review” to see the held lots, then open a lot for its quantity, expiry and reason for the hold.
Operations overview
Purchase decisions, stock checks and planned work.
Automation exceptions
| Record / work | Owner | Date | Status | Open record |
|---|---|---|---|---|
| QA release | 24 Oct 2026 | Pending QA release | ||
| Quality | 27 Oct 2026 | Quarantined | ||
| Purchasing | 30 Oct 2026 | Needs ordering | ||
| Purchase approver | 29 Oct 2026 | Awaiting approval | ||
| Stores lead | 28 Oct 2026 | Blocked |
Dashboard structure and work lists based on the system. All records shown are examples.
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.
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.
Project 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 |
Dashboard structure and work lists based on the system. All records shown are examples.
Routine checks, assigned tasks and recorded results
Forms & Monitoring
Replace separate check sheets and scattered results with configurable forms and a shared work list. Assign checks, record results, review submissions and use the collected information in reports.
Forms for your process
Define the questions and fields for recurring records such as equipment checks, inspections and operational logs.
Assigned and scheduled work
Give checks to the people responsible for completing them. See overdue tasks and work due next.
Structured entries
Record answers against the correct form so each completed check can be found and reviewed.
Submission review
See which entries need a reviewer and open the recorded answers before making a review decision.
Microbiology monitoring
Follow recorded samples and identify those still awaiting results or review in the monitoring module.
Reports from recorded results
Review the information collected across entries and use configured reports to monitor the process.
Explore the dashboard
Select “Task reviews” to open submitted checks, or “Awaiting Micro results” to see the samples still waiting for results.
Dashboard
Due work, reviews and Micro samples.
Overdue
| Record / work | Owner | Date | Status | Open record |
|---|---|---|---|---|
| Warehouse team | 27 Oct 2026 | Overdue | ||
| Production team | 30 Oct 2026 | Due soon | ||
| Quality reviewer | 29 Oct 2026 | Awaiting review | ||
| Warehouse reviewer | 29 Oct 2026 | Awaiting review | ||
| Microbiology team | 28 Oct 2026 | Awaiting results | ||
| Microbiology team | 28 Oct 2026 | Awaiting results |
Dashboard structure and work lists based on the system. All records shown are examples.
Validation
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 ↗Single systems and bundles
Choose the systems you need
Request one system or discuss several in the same quote. Tell us which teams will use them, what needs to be tailored and whether you need validation included in the scope.
Bespoke development
Spreadsheets, reporting tools and applications
Development for requirements outside the five systems. We can review an existing spreadsheet, build a report from your data or develop an application for a specific process.
Bespoke development servicesSpreadsheets
Data entry, calculations, repeated tasks and reporting.
Data and reporting
Data preparation, combined views and defined reports.
Workflow applications
Forms, assignments, review stages and records for your process.