Meet medical device quality and compliance requirements with better access to Standards
Rigid regulatory obligations leave no room for error in the medical devices industry. It's time to connect and empower your organisation with access to 1.6 million technical Standards and documents - all in one place.
Every department requires access to Standards, from legal and regulatory affairs, quality auditing, product development and more. Transform their access with i2i.
Custom access for specific projects and needs
Configurable features on our i2i platform make it easy to create a collection of Standards relevant to your medical devices sub-sector or area of product development.
Create customised collections of Standards to provide each team or department with only the Standards they need to help ensure best practices and improve collaboration.
Stay on top of changing Standards
Monitor ever-changing Standards updates and revisions specific to your Standards collections with timely email notifications of relevant changes to reduce compliance gaps.
Updated Standards versions are also added to your i2i subscription automatically, giving your team the ongoing access they need.
Cross reference company documentation with Standards
A well-managed Standards library can make a critical difference when managing risk. Streamline your Standards management by linking internal documents, policies, drawings, images and guidelines alongside your Standards, establishing an in-house knowledge base which can be developed for each user group or product being developed.
Enhancing how your organisation accesses Standards can boost productivity, ensure consistency, help your products and services remain compliant and gain a competitive edge in a challenging industry.