MetaMedical™ Solutions Inc

RQM+ launches AI module to enhance regulatory documentation

RQM+ has introduced the AI-powered Smart Authoring module, a significant addition to its platform, aimed at redefining regulatory documentation in the medtech sector.

This platform now includes Smart Authoring and Systematic Literature Review.

The new module is intended to improve compliance, accuracy, and efficiency in creating and managing regulatory documents.

Offering a groundbreaking solution to the complexities of regulatory documentation, the Smart Authoring module helps automate and streamline the creation, management, and maintenance of these critical documents, ensuring readiness for regulatory submissions.

RQM+ collaborated with AI technology company in developing the Smart Authoring module.

The module’s main features include smart keys and product profiles to provide a single source of truth for document version control; template management and alignment; dynamic linking across documents; enhanced team collaboration; and streamlined literature reviews.

Access the most comprehensive Company Profiles
on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free

Your download email will arrive shortly

We are confident about the
quality of our Company Profiles. However, we want you to make the most
decision for your business, so we offer a free sample that you can download by
submitting the below form

By GlobalData

Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

These capabilities are designed to reduce time-to-market for medtech products by accelerating document preparation.

RQM+ CEO John Potthoff said: “’s Smart Authoring module represents a significant leap forward for the medical device industry.

“By harnessing the power of AI and automation, we’re not only simplifying the creation, management, and maintenance of regulatory documentation but more importantly, it enables manufacturers to bring life-saving devices to market faster and with greater confidence. This platform is a game-changer for regulatory affairs professionals and the medtech industry as a whole.”

RQM+ said that the AI-driven platform minimises repetitive tasks and promotes consistency, allowing teams to concentrate on strategic activities that drive innovation and efficiency.

Source link