What is ISO 13485?In this post, we’ll discuss what ISO 13485 is all about, by whom it is used and what is important to take into account.Dec 11, 2023Dec 11, 2023
Why would you need a Digital QMS?Traceability is crucial for medical device manufacturers. Digital tooling that supports traceability is key to success.Dec 11, 2023Dec 11, 2023
FDA Issues Long-Awaited Proposed Rule To Regulate Laboratory-Developed TestsThe landscape of regulatory standards in the medtech industry is dynamic, with many updates that respond to advancements in technology…Dec 11, 2023Dec 11, 2023
Streamline your workflow with the enhanced Jira integrationDiscover upgraded Jira integration empowering streamlined workflow. Effortless ticket creation, enhanced communication, …Dec 11, 2023Dec 11, 2023
Enhancing the TEO Dashboard: A new level of testing visibility!The Test Execution Overview Dashboard (TEO Dashboard) is a valuable part of the Matrix ecosystem & we’ve been working to enhance its…Dec 11, 2023Dec 11, 2023
Agile Compliance at MedFITEntrepreneurs and startups within the Medtech and Medical Devices industry are often in the dark when it comes to the regulatory approval…Dec 11, 2023Dec 11, 2023
SBOM, CBOM, OTS, COTS, SOUP — The complete guideTo communicate about Software as Medical Device we need to understand the meaning of terms and abbreviations.Dec 11, 2023Dec 11, 2023
Decoding ALM and PLM: Where Do They Diverge?In the dynamic landscape of modern product development, two distinct methodologies have long held the reins: Application Lifecycle…Dec 11, 2023Dec 11, 2023
10 Essential Steps for Pre-Market Medical Device StartupsDiscover the essential roadmap for pre-market medical device startups. uncover the 10 key steps to success in this competitive market.Dec 11, 2023Dec 11, 2023
The power of review and approval workflows in your eQMSElevate SxMD Success: Streamline Quality, Bridge Design Gap, Ensure Compliance. Discover the Power of Review & Approval Workflows in an…Dec 11, 2023Dec 11, 2023
