There is an increasing drive and focus on the collection and use of real world data within the pharmaceutical industry. With advances in technology and personalised medicine, the demand for real world data to support the drug development lifecycle continues to gain momentum as well as support from regulatory agencies.
The field of real world data extends across a diverse spectrum of data sources from the unstructured (e.g. EHRs and wearables) to the more structured observational and registry studies. This webinar will focus on the data collection and system challenges in structured observational and registry studies collecting retro- and prospective real world data .
This webinar will:
- Present key challenges in data collection
- Review strategies and system features to help facilitate data acquisition
- Demonstrate effective management of data to ensure high quality and efficient data flow
- Discuss the maintenance of efficient data flows
- Draw examples from experience in oncology research
Speakers
Kirsten Bulpitt, Director of Clinical Data Management, Cmed Clinical Research Services
Kirsten has worked for over 20 years in Data Management, giving her a wide breadth and depth of experience within both pharma and CRO. This experience extends across an array of therapeutic areas from early phase through to real world settings. She has led the development of innovative processes and supported CDM teams with the subsequent training materials and adoption. As a key area of interest, Kirsten has supported the validation and implementation of new systems as well as the generation and adoption of technical solutions to support the acquisition and management of data in clinical research.
Message Presenter
Stéphane Forrer, Associate Director of Systems Management & Data Visualizations, Cmed Clinical Research Services
Stéphane has over 13 years’ experience of programming and validating clinical drugs trial databases and software. He is the System Owner for encapsia, Cmed’s cloud-hosted Clinical Data Suite and he leads a team of Visualisation Programmers to develop actionable Insights and visualizations to streamline the review of real world and clinical data.
Message PresenterWho Should Attend?
This webinar will be valuable for:
- Data Managers
- Data System Managers
- Real World Data Scientists
- Clinical Study Managers
within pharma, biotech and CROs
What You Will Learn
- Key challenges in data collection for Real World Studies
- Strategies and system features to help facilitate data acquisition
- Ways to manage data effectively to ensure high quality and efficient data flow
- How to maintain efficient data flows
Xtalks Partner
Cmed
Cmed provides specialist data and analytics services for clinical trials with over 350 staff globally. The company has delivered over 700 studies across all phases with clients from top 10 pharma companies to small biopharma.
Cmed has experience in managing large registry studies, understands their unique challenges and uses technologies including encapsia to optimize complex data flows to allow greater flexibility and provide real-time visual access to all study data. www.cmedresearch.com
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