2022 - The Importance of Data Integrity and Accessibility in Successful Clinical Trial Management
Date2022-11-17
Deadline2022-11-17
VenueWebinar, USA - United States
KeywordsPatient Data; Clinical Data Management; Clinical Trial Management
Topics/Call fo Papers
A Chat with Industry Experts in Quality and Data Management about how Data is Reshaping the Industry
In today’s digital world, data is king, and the future is in robust systems and processes that ensure data integrity and value. Within the clinical trial industry, data is collected in many formats, and it must be filtered and managed to be useful. Controlling how it is stored, accessed and ultimately used is all part of assuring data reliability and protecting the safety of patients and the quality of the drugs created.
In this webinar, the featured speakers will talk all things data — how it’s relevance and accessibility has flourished, how it’s shaping the clinical trial industry and the expected growth of data strategy as technologies and the roles in data management evolve.
Register for a chat with industry experts in quality and data management about data integrity and accessibility for successful clinical trial management. We invite you to submit your topics and questions in advance for the discussion.
In today’s digital world, data is king, and the future is in robust systems and processes that ensure data integrity and value. Within the clinical trial industry, data is collected in many formats, and it must be filtered and managed to be useful. Controlling how it is stored, accessed and ultimately used is all part of assuring data reliability and protecting the safety of patients and the quality of the drugs created.
In this webinar, the featured speakers will talk all things data — how it’s relevance and accessibility has flourished, how it’s shaping the clinical trial industry and the expected growth of data strategy as technologies and the roles in data management evolve.
Register for a chat with industry experts in quality and data management about data integrity and accessibility for successful clinical trial management. We invite you to submit your topics and questions in advance for the discussion.
Other CFPs
- Potency Assays for ATMPs — Conception, Development, Validation, Matrixed Approaches and Assay Lifecycle
- EConsent — Driving Successful Adoption
- The Changing Face of Trial Recruitment: Site-Only and Recruitment Provider Options
- Radiation Toxicity — Considerations for Implementing Radiation Dose Limits in Radiopharmaceutical Trials
- Emerging Applications for Liquid Biopsy in Drug Development
Last modified: 2022-11-02 02:08:13