Cyntegrity is hosting the RQA 2026 conference in London
Public source
Publisher name
Public post
The conference season is coming. Let's meet in London The #RQA 2026: https://lnkd.in/eHJ2MFYt
Company
Cyntegrity
AI-augmented RBQM | Predictable Trials | Human-in-Control Oversight
- Industry
- IT Services and IT Consulting
- Location
- Frankfurt, DE
- Company size
- 11–50 employees
About Cyntegrity
Cyntegrity enables predictable, inspection-ready clinical trials with AI-augmented Risk-Based Quality Management (RBQM) that goes beyond automation. Our technology supports human decision-making, not replaces it — preserving historical oversight records for full traceability over time, ensuring teams understand not only what changed, but why. Our MyRBQM® Portal provides portfolio-wide oversight—from protocol complexity analysis to patient-level signal detection—while our MyRBQM® Academy builds shared understanding and practical capability across study teams, CRO partners, and QA groups. We support sponsors, CROs, and regulators in operationalizing ICH E6(R3), E8(R1) and Q9(R1) consistently and at scale, ensuring that quality oversight remains fit-for-purpose, defendable, and future-proof. Powered by a diverse, international team, we help organizations evolve from reactive checks to predictive, insight-driven, human-in-control oversight that strengthens compliance, decision traceability, and resource focus across studies and portfolios.
See moreLatest activity
Latest activity from Cyntegrity
9 signals
Presence & Recognition
Cyntegrity announced that Keith Dorricott and Dr. Johann Proeve will be presenting a webinar on Measuring Risk in RBQM on 24 September.
Research & Knowledge
Cyntegrity published an interview with Adam Baumgart reflecting on a recurring implementation challenge regarding effective risk management in RBQM.
Legal & Regulatory
Cyntegrity is contributing its experience in QbD, RBQM, and technology-supported quality oversight to the discussion on FDA communication regarding inspection and risk-based criteria for selecting sites in global clinical trials.
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