Meet Nubilaria at the key conferences shaping clinical data and life sciences
In 2026, Nubilaria will be present at a curated selection of clinical research, clinical data management, and life-science partnering events across Europe and beyond.
Our goal is simple: create meaningful conversations with CROs, sponsors, pharma companies, biotech innovators, and research organizations—and show, in a practical way, how the ACTide eClinical Ecosystem supports modern, compliant, and data-driven clinical research.
Want to meet us at one of the events below?
➡️ Book a meeting and tell us your focus (EDC/eCRF, ePRO, eTMF, AI reporting, trial operations, data governance).
Why meet ACTide in 2026
- What you can expect from our event presence
- Live conversations with both commercial and technical profiles: from strategic fit to operational feasibility.
- Concrete demos at selected events: see ACTide in action and discuss your trial data workflows.
- A roadmap-driven perspective: we’ll share how we’re evolving the ecosystem to support real-world CDM needs.
- Focus on what matters to CROs and Sponsors: quality, traceability, faster setup, and better control over data processes.
Where to meet us: Event calendar 2026
February 2026
EUCROF 2026 — Amsterdam, NL (Feb 2–3, 2026)
Participation: Exhibitor — Booth B21
Demo session: Yes (20-minute format)
What to discuss: Clinical data workflows, ecosystem approach, operational efficiency, demo of key capabilities.
➡️ Book a meeting at EUCROF
SCOPE Summit 2026 — Orlando, FL (Feb 2–5, 2026)
Participation: Attendee
What to discuss: Outsourcing models, CRO needs, clinical operations trends, and how ACTide supports scalable CDM.
➡️ Schedule a quick intro during SCOPE
March 2026
ACDM Conference 2026 — Berlin, DE (Mar 16–17, 2026)
Participation: Exhibitor — Stand 26
Demo session: Yes (40-minute format)
What to discuss: Clinical data management best practices, operational workflows, and how ACTide supports data-driven research.
➡️ Meet us at ACDM (book a slot)
Generative AI nelle Life Science — Milan, IT (Mar 26, 2026)
Participation: Attendee (in progress)
What to discuss: AI in clinical data management, future-proof reporting, and the role of AI in quality and efficiency.
https://www.aboutpharma.com/evento/generative-ai-nelle-life-sciences-2026
April 2026
Nutrition & Growth — Prague, CZ (Apr 9–10, 2026)
Participation: Exhibitor (TBC)
What to discuss: Clinical research operations for nutrition studies, patient data collection, and integrated eClinical workflows.
https://nutrition-growth.kenes.com/
German Biotechnology Days — Leipzig, DE (Apr 21–22, 2026)
Participation: Attendee (TBC)
What to discuss: Partnering and collaboration opportunities with biotech teams, research orgs and service providers.
https://www.german-biotech.day
May 2026
Swiss Biotech Day — Basel, CH (May 4–5, 2026)
Participation: Attendee (TBC)
What to discuss: Swiss market opportunities, partnering, clinical trial digitization, and compliant data ecosystems.
UK Biotech Day — London, UK (May 27–28, 2026)
Participation: Attendee (TBC)
What to discuss: Growth partnerships and operational solutions for biotech clinical development.
June 2026
WHX Miami (FIME) — Miami, FL (Jun 17–19, 2026)
Participation: Exhibitor (TBC)
What to discuss: International visibility, new opportunities in digital health, and scalable clinical data solutions.
https://www.worldhealthexpo.com/events/healthcare/miami/en/home.html
October 2026
CPhI — Milan, IT (Oct 6–8, 2026)
Participation: Attendee (TBC)
What to discuss: Pharma ecosystem touchpoints, collaborations, and how ACTide supports regulated data processes.
https://www.cphi.com/europe/en/home.html
World Orphan Drug Congress Europe — Amsterdam, NL (Oct 26–28, 2026)
Participation: Attendee (TBC)
What to discuss: Rare disease clinical development needs, patient-centric data collection, and compliance-driven processes.
https://www.terrapinn.com/conference/world-orphan-drug-congress/?
November 2026
BIO-Europe — Cologne, DE (Nov 09-11, 2026)
Participation: Exhibitor/Attendee (TBC)
What to discuss: Partnering, business development, and eClinical ecosystem strategy for CROs and sponsors.
What we’ll showcase
The ACTide eClinical Ecosystem: modular, scalable, ready for real-world trials
ACTide supports organizations that need robust and traceable processes across the clinical data lifecycle—through a modular ecosystem that can adapt to different trial designs and operational models.
Typical discussion topics at our events:
- EDC / eCRF workflows and study setup
- Patient data collection with ePRO
- eTMF alignment and operational readiness
- Data governance, quality control, and compliance-friendly processes
- AI-enabled approaches to improve efficiency and unlock insights
Book a meeting with our team
We’ll reply within 1–2 business days to confirm a time slot.