R&D, management reviews and business oversight
Governance
Bring R&D tracking, quality management reviews, intellectual property, and strategy, tenders and business oversight together. See upcoming decisions, commitments and review dates, with the records and actions behind them.
For directors, quality leads and teams responsible for R&D, commercial decisions and business oversight.
From £399 per month for 1–15 named users. VAT where applicable; implementation quoted separately.
Prices, user bands and packages ↗What you can manage
Quality management reviews
Prepare review agendas and reports, record decisions and assign follow-up actions. Keep the review history and supporting evidence together.
R&D tracking
Record research and development activities against identified projects. Keep technical uncertainties, work carried out and supporting evidence available for review.
Intellectual property
Maintain an IP register with ownership, status, supporting records and renewal or review dates.
Tenders and bid decisions
Record customer tenders, deadlines and bid/no-bid decisions. Assign requirement responses, track clarifications and internal approval, then record external submission and the outcome.
Strategy and business development
Assess opportunities and feasibility before work becomes a project. Record customer visits, decisions and the actions needed to progress the opportunity.
Regulatory commitments and continuity
Track regulatory obligations, business risks and continuity plans. Assign owners, review dates and actions so open commitments remain visible.
Management actions and reporting
Review upcoming dates and outstanding actions across Governance. Use manual records and configured imports to bring supporting information into management reviews.
The application dashboard
See the interface used to review work and priorities.
Enlarge 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 ↗
