Addressing Challenges in Drug Development – A Case Study
A case study illustrates how compliance and quality can be enhanced through real-time visibility into study conduct in a multi-site trial.
Managing Multi-Center Trials in Clinical Research — Q&A (Part 1)
Representatives from the Harvard Cancer Center answer questions about conducting trials within its consortium, as well as with unaffiliated sites.
Key Enhancements in Allegro CTMS Remain Focused on the User Experience
Influenced by customer feedback and industry needs, Allegro CTMS received key enhancements that enrich the user experience and optimize operations.
Yale University Deploys Integration Between its EMR and Forte’s OnCore
Interfaces facilitate communication of protocol and subject information, and research billing designations.
New EDC System from Forte Offers Affordable Sophistication
Forte announces their newest product, an EDC system ideal for researchers with tight budgets and a desire to get started quickly.
Best Practices in Pre-Screening Includes Use of Technology
Pre-screening subjects is common practice at most sites. In this article, learn some best practices and how technology can play an important role.
Technology’s Role in Addressing Challenges in Drug Development
There are opportunities to improve drug development by providing the right tools to sites, where much of the work of clinical research is conducted. Part 1 of 2.
Forte Adds Effort Tracking Tool to Suite of Free Resources
Three months after announcing the Site Metrics Registry, Forte has launched a new free resource for sites, the Effort Tracking Tool.
Practices for eCRF Design: Defining Roles and Responsibilities
Zeena George and Sarah Strange discuss how the Children’s Hospital of Philadelphia has streamlined coordination around the design of eCRFs.
Maintaining a Positive Cash Flow at your Research Site
Gina Robles, of PharmaSeek Financial Services, discusses the importance of sites maintaining positive cash flow and how it can best be achieved.