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Top Reasons to Attend Inspection Readiness by Clinical Document World
Three days of live interactive sessions covering inspection readiness best practices.
Implement new technologies that positively impact an organization's quality, monitoring, and metrics to ensure TMF completeness.
Get all of your questions answered through live speaker Q&A following every session, or during networking breaks in the virtual networking lounge.
Hear from 20+ industry leaders representing Sponsors, Sites, and CROs
An in-depth workshop on how to strategically prepare for a remote inspection will be hosted on the first day of the event, make sure to purchase an 'All Access' pass to get access to all three days of the event!
A virtual interactive environment that will allow you to network and learn with industry colleagues.
Who Should Attend
Life Science professionals from pharmaceuticals, biotech, and medical device organizations with responsibilities in:
- Inspection Readiness
- Quality Compliance / Management / Assurance
- Clinical Documentation
- Trial Master File
- Clinical Operations
- Trial, Records, Document Management
- Clinical Technology
- Risk Management
- Clinical Trial Management
Sponsoring the Summit
The Clinical Document World Event is the premier event to meet Clinical Documentation, Trial Master File, GCP, Clinical Quality professionals who are looking to improve their processes through strategic improvements and partnerships. Learn more about how we can create a unique sponsor experience for your company. Please contact Kelly Hara.