If you are on the front lines of regulatory information management within the life sciences industry, you know how important it is to keep organized, move fast, streamline internal collaboration, and prepare for the future. Regulatory affairs is an essential part of the drug development process, as it ensures organization-wide compliance with all applicable global legislative and regulatory requirements at each stage of the product development cycle.
To help make regulatory affairs easier to manage, ArisGlobal is excited to announce the release of LifeSphere Regulatory. This is an all-new cloud platform that provides full end-to-end regulatory management within an easy and unified suite. The platform:
- Minimizes risk and stays up-to-date with the latest regulations utilizing modern cloud architecture, and provides free upgrades, thereby future-proofing compliance.
- Is built using innovative automation capabilities, allowing all regulatory tasks to be done using a single, easy-to-use interface.
- Is Identification of Medicinal Products (IDMP)-ready out of the box, unlike other RIMS applications.
At ArisGlobal, we also understand the importance of effective and streamlined collaboration when managing regulatory information. To that end, LifeSphere Regulatory is easily unified with drug development applications to streamline cross-functional collaboration and provide a single source of truth across the entire organization.
Let’s have a conversation together so we can tell you more! You can also learn more about LifeSphere® Regulatory just by visiting https://www.arisglobal.com/products/lifesphere-regulatory/.
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