What is Consinova?
Consinova provides pharma software for quality, equipment, stock, projects and operational records, alongside bespoke software development. The systems can be purchased individually or as a package.
Consinova systems
Pharma software
Pharmaceutical software for quality, equipment, stock, projects and operational records. Choose individual systems or a package, 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
- Corrective and preventive actions
- Change control
From £299 / month 1–15 named users
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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
- Calibration schedules
- Maintenance and revalidation
From £199 / month 1–15 named users
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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
- Purchase orders and approvals
- Goods receipt and QA release
From £495 / month 1–15 named users
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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
- Reusable project structures
- Actions and responsibilities
From £149 / month 1–15 named users
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Routine checks, assigned tasks and recorded results
Forms & Reporting
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
- Assigned and scheduled work
- Structured entries
From £299 / month 1–15 named users
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Choose the systems you need
Reduced package pricing is available for two or more systems. All five start from £1,300 per month for 1–15 named users. View prices and user bands ↗
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 ↗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.
Questions about Consinova
Software, pricing and implementation
Is Consinova only for pharmaceutical businesses?
Pharmaceutical businesses are our main focus. We also consider requirements from other industries, including spreadsheets, reporting tools and workflow applications.
How much does Consinova cost?
Individual systems start from £149 to £495 per month for 1–15 named users. The five-system package starts from £1,300 per month. Prices are in GBP, excluding VAT where applicable. Implementation is quoted separately.
Can I combine systems?
Yes. Reduced package pricing is available for two or more systems. Your quotation lists the selected systems and total subscription. Buying several systems does not imply that every workflow or data source is automatically integrated.
Can the systems support a validated pharmaceutical process?
The configured system must be assessed and validated for its intended use. Validation scope, responsibilities, testing and evidence are agreed for each implementation; purchasing software does not itself validate the process.