Creating processes that result in accurate, timely and complete data are invaluable when implementing or optimizing a CTMS. Here are a few tips to achieve your goals.
This Clinical Trials Day, we want to celebrate the contribution made by your clinical research coordinators, and provide actionable ways to provide them with a fulfilling work environment.
Coordinating centers often struggle with the administrative burden of managing regulatory documents across multiple participating sites. We collaborated with our customers to address this challenge through the Forte eRegulatory Management System.
Forte and ACRP partnered to conduct a survey analyzing the factors that contribute to technology competency and how sites, technology providers and clinical research professionals can work to improve these competencies across the industry.
Professional development and education are required in a vast array of industries, including clinical research. Continuing education units (CEUs) are a great way to have a record of your ongoing educational accomplishments.
How Managed Infrastructure Can Provide a Secure, Sustainable Foundation for Your Research Technology
Utilizing a vendor-managed infrastructure can help you maximize internal resources, improve technical support, boost security and improve user experience for your enterprise software.
Protocol calendars drive a wide array of study-related activity for teams throughout your organization. To keep your study startup processes on track and ensure quality calendars, it’s important to optimize your calendar-building staff and your processes.
Learn the qualities of an ideal CRA and the necessary competencies for success in the clinical research industry.
Expert webinar presenter answer attendee questions about the tool she developed to assess clinical trial staff workloads.