Thought Leadership
C3 Summit San Francisco
AC Hotel 1333 Veterans Blvd, South San Francisco, CA 94080 San Francisco, California...
IMP Labeling: EU CTR Transition Considerations
The blog post explores the critical aspects of transitioning Investigational Medicinal Product (IMP) labeling from the EU Clinical Trial Directive (EU CTD) to the new EU Clinical Trial Regulation (EU CTR). ...
7 Considerations for Improving the App Localization Process
App localization can be a complex process, especially for life sciences organizations. With many apps designed with patient experience in mind, such as patient portals designed for the collection of health data and tracking patient journeys, it's critical that...
Considerations and Opportunities in Capturing Oncology Patients’ PRO Data
There has been a historic lack of guidance in capturing patient data for oncology patients. Join Bill Byrom, VP and eCOA Scientist at Signant Health in conversation with Mark Wade, Global Practice Leader at TransPerfect, as they discuss: - The need for specificity of...
Assessing Readiness for EU Clinical Trials Regulation (CTR): Five Points to Consider
Assessing Readiness for EU Clinical Trials Regulation (CTR): Five Points to Consider...
Considerations for Improving the Pediatric Experience
The rare disease space presents numerous challenges for clinical research and patient data capture. These challenges are only heightened for younger patient populations, where outcome measures and dosages need to be considered appropriately. Join Dr. Elin Haf Davies, Founder &...
Building a Successful Partnership: Meeting Sponsor Expectations
To improve clinical trial electronic system development, strong partnerships must be built and maintained between key stakeholders to establish centralized consensus and alignment for high-quality electronic data capture. Join Aaron McCormick, Associate Director, eCOA...
Plain Language Summaries Checklist
Download your copy of our Plain Language Summaries Checklist....
Driving Digital Excellence: Delivering Seamless and Personalized Customer-Centric Experiences
The digital evolution in reaching and engaging with global communities, including sponsors, CROs, patients, and HCPs, has drastically shifted the way medical affairs teams connect with key stakeholders. As the industry pursues ways to improve a consumer and patient-centric...
Veeva Vault & Translation Management System (TMS) Integration
As pharmaceutical companies implement one or more Veeva Vault applications, it is important to consider the global aspect of content. Download our simple checklist to see if your organization could benefit from a connector between Veeva Vault and a TMS....
A Checklist for eCOA Solution Deployment: Best Practices and Considerations
Selecting and deploying a new eCOA solution involves many important factors - from determining the capabilities of the Language Service Provider (LSP) to identifying the technology used for each COA migration - and it’s impossible not to worry about missing a key detail in the...
