How to never miss a thing about your eTMF documents

CROs work in a fast-moving and highly complex environment. They manage multiple studies at the same time, often for different sponsors, across different countries, sites, and timelines. Each study comes with its own processes, reporting needs, and regulatory expectations. As this complexity grows, it becomes harder to keep everything aligned using separate tools or spreadsheets […]

Risk management used to live in spreadsheets, scattered documents, and endless review meetings.Not anymore 👀 That’s exactly what our QA Director, Anna Petrovskaya , will be speaking about at the International QA Virtual Conference. Her session,▶️ “Risk Management Automation in the GCP R3 Era,”will explore why traditional, document-based risk management approaches are no longer enough, and […]

We’re heading to Barcelona for OCT 2026. And this time, we’re bringing a real story with us! Our colleague Evgenia will be speaking alongside Jaume Costa from SOLTI, our dear client and long-term partner, about the question many teams still struggle with: Who should own your eClinical systems: sponsor or CRO? Stream B: AI & […]

Blinded studies are critical for maintaining the integrity of clinical trials. But while the concept is straightforward, the operational reality is often anything but. For many clinical teams, managing blinding means dealing with: This creates a constant burden: Even with strict processes in place, a single misconfiguration can compromise the entire study. TMF Blinding in […]