Tidligere arrangementer

Trials@Home prosjektet ble avsluttet med publisering av et sett anbefalinger for vellykket implementering av desentraliserte studier i Europa. 

Avslutningsvis ble det arrangert en konferanse dedikert til prosjektets anbefalinger. Programmet for konferansen:

• Trials@Home key final recommendations  
• Trials@Home deep dive
• Impact in the DCT field
• The future of DCT

DMP har holdt en serie webinarer om medisinsk utstyr, blant annet;

• Introduksjon til medisinsk utstyr (opptak av webinaret )
• Når programvare er medisinsk utstyr (opptak av webinaret )
• Klinisk utprøving av medisinsk utstyr i samarbeid med REK KULMU (opptak av webinaret )
• Nytt regelverk for produkter uten medisinsk formål (opptak av webinaret )
• Egentilvirkning av medisinsk utstyr (In-house) (opptak av webinaret )

Opptak og presentasjoner fra gjennomførte webinarer er tilgjengelig

EU-kommisjonen arrangerete 21. mai 2025 en workshop om EUDAMED. Der ble det blant annet gitt en introduksjon til regelverket, databasen, tidsplanen for utrulling, oversikt over funksjonalitet og en gjennomgang av de ulike modulene. Opptak og presentasjoner av dette ligger nå ute på kommisjonens sider. 

Agenda for arrangementet:

• Welcome to ICTD 2025
• Setting the scene
  • What is inclusivity? Defining the key words for a common understanding
  • Why inclusion matters in clinical trials
• Stakeholder perspectives (Part I)
  • Psychiatric exclusion criteria in clinical research: bridging the ethical and health need divide
  • Ensuring inclusivity in study design: an ethics perspective
• Panel: Engaging with the underserved populations, what works?
• Stakeholder perspectives (part II)
  • How can regulators influence inclusivity in clinical research?
  • What is the pharmaceutical industry doing to make trials more inclusive?
• Inclusivity in practice
  • The importance of clinical trials in pregnancy
  • Striving for scientifically representative trials
  • From access to empowerment: inclusive practice in clinical trials
• Panel: Building a clinical trials environment to support inclusivity
• Working towards new solutions: READI project sets the precedent

Agenda for arrangementet:

• Welcome to ICTD 2024
• Pillars of data-centric clinical research
  • Real world data in clinical research - the medical perspective
  • Digital solutions for leveraging clinical research
• Novel approaches to data-centric clinical research - relevant examples
  • Reusing sensitive data in public health research: a federated approach
  • Reusing health records in clinical research: the Ecream project
• Multi-stakeholder perspective to data-centric clinical research - part I: Industry and the authorities
  • Data-driven innovation in the pharma industry
  • Reinventing drug safety in the view of real-world data
• Multi-stakeholder perspective to data-centric clinical research - part II: Patients and society
  • Patient-centric equals data-centric? On which conditions?
  • From patient empowerment to opt-out: What is the role of patients in recent research legislation?

Agenda for arrangementet:

• Welcome to ICTD 2023
• Multistakeholder Perspektive
  • EU recommendations on desentralised elements in clinical trials
  • Desentralised clinical trials - Industy perspective
  • Decentralised clinical trials - a Patient perspective
• The Trials at Home project: What have we learned about decentralised clinical trials in Europe?
• Operational and technological approaches
  • e-Consent: not a one size fits all
  • Taking part in trials without leaving your own bed: experience from PRINCIPLE and PANORAMIC
  • Using decentralised elements in a pediatric trial
• Panel session: Future of patient participation: conventional, hybrid, fully decentralised