Explore our end-to-end, full service clinical development capabilities including Therapeutics expertise, Development Planning, Phase I early clinical development, Phase IIb/III and Phase IV Trials, Regulatory Submission and Post-Launch Studies.
ACDM23 offers a full two day programme of expert speakers, specialist panels, workshops and debates which will focus on the current topics in the field of clinical data management. It will enable sponsors and exhibitors to maximise their exposure and opportunities at what is always a rewarding and vibrant event.
Visit us at stand #31 during the event to say hi to our team.
Nina Reyes from our data management team with be presenting on the first day at 11:30 on:
External Sources, how to be best integrated into our Data Management landscape – Where in today's clinical trials increasingly turn to third party data sources to collect study data. Electronic data capture (EDC) accounts for only 20-40 percent of all clinical data collected, which requires an innovative data management team to ensure transparency, data integrity and quality of the data. Efficiently controlling this high level of complexity and avoiding delays in achieving a database lock requires a strategic approach and adequate technologies like true intelligent connections and a Clinical Data Repository (CDR) that ingests, integrates, and standardizes data to drive downstream processes such as Real-Time Data Cleaning, Decentralized Trails, Centralized Monitoring, and machine learning. Because our industry data needs to go beyond numbers and become true insights instead
We will also be demonstrating the latest innovation from across data management in a 1hr demo session on the Wednesday at 14:30 – 15:30 in the Diagonal Demo Room please come and join us if you can.
Explore our end-to-end, full service clinical development capabilities including Therapeutics expertise, Development Planning, Phase I early clinical development, Phase IIb/III and Phase IV Trials, Regulatory Submission and Post-Launch Studies.
Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.
Change the model of clinical research by integrating data, expertise, analytics and technology from study design through execution to power better decisions.
Improve the performance of your clinical trials with the power of the IQVIA CORE.
Ensure you have access to insights early with connected devices and clean, analysis-ready data