October 13, 2022Reducing the time for medical writers to create regulatory documents
As a medical writer, you know that time is a valuable resource. Writing high-quality and accurate medical regulatory documents can be a time-consuming and complex process, and it is essential to find ways to streamline and optimize your workflow. One powerful tool that can help you achieve this goal is the use of specialized software like the Otium Regulatory DocWriter™.Read more
October 13, 2022Medical Writing Software
Medical writing software is must-have; however, until now medical writers have had few good options. In particular, there has not been any software designed to efficiently cut down on the time required to produce regulatory documents.Read more
October 13, 2022Otium will be at the CTO 2022 Conference
Otium will be attending the CTO 2022 Clinical Trials Conference.We would love to see you November 10 & 11, 2022 in Toronto! Please drop by our booth to see a demo of our new Regulatory DocWriter™ software. We hope to see you there!Read more
October 13, 2022Announcing Otium Regulatory!
Otium is developing a Software as a Service product named Regulatory DocWriter, an online document writing platform, which automates the regulatory writing component for Investigator Brochures (IBs), Clinical Study Reports (CSRs), Clinical Study protocols, Informed Consent, Trial Disclosure Forms, and similar documents. The generation of these standard documents is one of the most time-consuming stages in the development, testing and approval of new drugs, taking weeks and in some cases months to complete.Read more
Regulatory DocWriter™ is the professional regulatory writing platform.
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