Clinical.ly provides differentiated technological solutions to the clinical research industry, helping research facilities focus on conducting studies as efficiently as possible. We’re working hard to provide modern, intuitive software that frees up resources and reduces headaches. As trials keep evolving in complexity, it is becoming more apparent that the same old procedures aren’t keeping up. Inspection findings are much more costly than adopting the right technology, procedures and best practices.
The clinical trials industry is ready for better tools to help stay ahead of the evolving demands of sponsors and regulators.
We work closely with clinical trials facilities to understand their SOPs and provide solutions to help address their nuanced needs. By integrating your proprietary workflows, we help remove barriers to adoption and help you focus on your primary responsibilities. Free your medical staff to focus on the jobs you hired them to do.
eRegBinder by Clinical.ly is a purpose-built solution designed to help organizations meet regulatory compliance requirements in clinical trials. The system reduces mistakes by tracking required documents, signatures, and timelines, as well as offering automatic alerts on missing data. With electronic delegation and training logs, and remote monitoring access your time spent on regulatory compliance is minimized, helping you avoid spending employee time on fixing mistakes, omissions or missing information.
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Regulatory Overburden and the Role of eRegulatory Systems
If you are reading this, you don't need us to tell you that regulatory obligations are time-consuming, nuanced, and carry serious negative consequences if not performed with surgical precision. Yet, at some of the organizations with whom we have the privilege of working, there is a disconnect between those tasked with fulfilling regulatory obligations and the rest of the clinical and administrative staff who never opened a regulatory binder.
Our partners requested we write a summary of day-to-day regulatory obligations and how an eRegulatory platform might help address them. Please read our latest publication on regulatory challenges and the value of an excellent eRegulatory platform.
Cybersecurity in the Remote Age
With a shift to digital technologies and remote monitoring comes an increased risk of cyberattacks. With many organizations working remotely, cybersecurity awareness has become even more crucial. How can you and your organization avoid becoming victims?
To support the research community, Clinical.ly has created this practical and actionable guide. You'll find tips inside, such as:
Suggestions on how to increase your organization's security awareness
Options for creating and storing secure passwords
Surefire ways to spot malicious emails
How to be alerted if your password is compromised
eRegBinder by Clinical.ly Infographic
eRegBinder by Clinical.ly is a purpose-built solution designed to help organizations meet regulatory compliance requirements in clinical trials. The system reduces mistakes by tracking required documents, signatures, and timelines, as well as offering automatic alerts on missing data. With electronic delegation and training logs, and remote monitoring access your time spent on regulatory compliance is minimized, helping you avoid spending employee time on fixing mistakes, omissions or missing information.
