Clinical Trial Technologies and Data Integration Conference

After extensive research with data and technology experts within clinical research, the question you are all asking is clear – are you getting the best out of our current data systems?

While EDC is widely used within the industry, what is the next step? How can you ensure that your computer systems ‘talk to each other’ effectively?

Informa Life Sciences is delighted to give you advanced notice of the inaugural Clinical Trial Technologies and Data Integration Conference. Topics will range from data management standardisation and validation, through to easier access to integrated data from various sources, including ePRO and EHR.

• Integrating and converging systems used by CROs, sponsors and sites, including the possibility of a 'single system'
• Leveraging value from real-time data integration
• Electronic Data Capture and clinical Outsourcing: Governance in multiple CRO partnerships relations
• How technologies will relieve costs, aid compliance and speed up processes
• Implementing integrated data flows in the exchange of information
• Share point portals for all document management and exchange of information
• Integration of CTMS with your EDC system
• Linking IVRS with the rest of your eclinical tools data management
• European regulatory authority perspective on AE (Adverse Event) reporting and common findings in clinical trials
• Overcoming challenges in compliance with the recently published EMA reflections on e-source  and on the new EU Annex 11 revision
• Achieving quality in your eclinical system
• Demonstrating compliance to regulatory bodies
• Case study: Leveraging EHR data to improve protocol designs, avoid protocol amendments, avoid site closures and enhance patient recruitment
• An introduction to Cloud Computing in clinical research