6 key elements to writing a strong clinical trial protocol synopsis
A clinical research protocol is a roadmap. In order to have a clear roadmap, it is important for the investigator to have […]
Protocol Builder Launches Individual License Option
Cloud-based solution allows investigators to simplify the development of clinical research protocols (Lake Success, NY) — Protocol Builder, the cloud-based solution for […]
Why Clinical Research Protocol Templates Don’t Work
Writing investigator-initiated clinical research protocols can be a time-intensive and daunting effort. Investigators agree that writing protocols is difficult and time consuming. What are the key obstacles for researchers who want to write a protocol that meets IRB standards? How can institutions go beyond templates and investigator training to speed up the process of developing and reviewing protocols?
Common Protocol Development Errors (Part Three)
In the last of this three-part series, we explore common types of information or documentation that may be inconsistent in investigator-initiated protocol submissions to an IRB.
Common Protocol Development Errors (Part Two)
In this, the second in a three-part series, we will look at the typical types of information or documentation that may be missing in investigator-initiated protocol submissions to an IRB.
BRANY launches software, iPad app to streamline protocol creation for investigator-initiated trials
CenterWatch, the leading source of clinical trials information for clinical research professional and patients, announces the launch of Protocol Builder. Read the full article.
BRANY launches Protocol Builder™ for investigator-initiated clinical trials
Web-based and iPad tablet application solution for writing investigator-initiated research protocols (Lake Success, NY) — BRANY has announced the launch of Protocol […]