News

As we celebrate Women's History Month and International Women's Day (March 8th), it's important to recognize the contributions of women in STEM fields.

Collaboration has become a key aspect of modern work, and the digital era has completely transformed the way we collaborate. Gone are the days of endless emails, confusing file versions, and endless meetings.

There are many paths that can lead to a career in medical regulatory writing. Lets take a look at some of the options to help pave the way for success.

Lets explores the nuances of regulatory writing in the medical writing industry and its unique requirements compared to other types of medical writing.

We take a look at the etymology of Otium and how it relates to modern Regulatory Writing.

Starting and running a successful freelance medical writing business takes a lot of hard work, determination, and patience. Here are some key skills you'll need to make it happen.

Medical regulatory documents play a vital role in ensuring that medical products and services are safe and effective for patients. The role of regulatory writers is to provide clear, accurate, and concise information to regulatory agencies for decision making about the approval and regulation of medical products.

Oitum Regulatory DocWriter was born out of the challenges we faced in our own regulatory writing work. We wanted to find a way to make the process easier and more efficient, and that’s exactly what we’ve created.

Holiday

As we kick off a new year, it's a great time to think about our goals and what we want to achieve in the coming months. We are excited to introduce Otium Regulatory DocWriter. Let's take our regulatory writing to the next level in 2023!

Benefits

October 13, 2022

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™.

October 13, 2022

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.

Conference

October 13, 2022

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!

Announcement

October 13, 2022

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.