White Papers

Mar 14, 2019
Sponsored Content
• How a free picking IRT can help significantly reduce costs and improve quality • Steps to manage supplies efficiently, with minimal risk, over a clinical program
Mar 14, 2019
Sponsored Content
• How AstraZeneca and MedImmune switched to SmartSupplies and cut costs by 10-20% annually • Learn how to take control of your clinical supply forecasting process
Mar 14, 2019
Sponsored Content
• Delve into accommodations for complex protocol requirements • Get best practices for deployment processes • Address integrations with other clinical systems and consultancy services
Mar 06, 2019
Sponsored Content
By Rho
Right-to-Try has been in the news a lot recently, but what does it mean for product sponsors? This white paper explores both Right-to-Try legislation and existing FDA Expanded Access Programs.
Mar 05, 2019
Sponsored Content
Early phase trials do not offer therapeutic benefit for the subjects is a specific drawback. However, special populations and patient cohorts are increasingly included early on. Read more about solutions.
Feb 07, 2019
Sponsored Content
• Determine key criteria for your successful eCOA study • Learn about the range of eCOA modalities currently available • Identify the best modality for your participants, site staff and study
Feb 07, 2019
Sponsored Content
• Learn where to start when implementing eCOA • Identify key stakeholders early and get insights on encouraging their involvement • Get guidelines on how to identify and assess quality eCOA partners
Feb 01, 2019
Sponsored Content
• 17 clinical research experts weigh in on trends they see developing in 2019 • Topics include: regulatory oversight, study designs, data & technology • Clinical site issues, clinical safety, pharmacovigilance, & gene therapy
Jan 22, 2019
Sponsored Content
• Human challenge studies allow researchers to assess vaccine efficacy • Discussion of human versus animal studies for influenza research
Jan 04, 2019
Sponsored Content
• Identify what components of eConsent support patient centricity • Recognize best practices for the design of an eConsent solution to best support the study patient • List what aspects of eConsent best support recruitment, retention and compliance
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