by Jeremy Moore | Mar 10, 2025 | Quality Management, Compliance and Regulatory Guidance, Software as a Medical Device
Compliance, but Make It EffortlessThe Problem with Traditional QMS PlatformsHow Fission Changes the Game1. Flat-Fee Pricing: Predictable, Transparent, and Scalable2. A Living, Breathing Compliance System3. Compliance That’s Always-On (Not a Last-Minute Fire Drill)4....
by Jeremy Moore | Dec 26, 2024 | Quality Management
Quality is the Secret Sauce, Not the SlogKey Building Blocks for a Quality CultureActionable Strategies to Foster a Quality CultureSustaining a Culture of QualityThe Competitive Edge of a Quality Culture Quality is the Secret Sauce, Not the Slog Some companies chase...
by Jeremy Moore | Aug 27, 2024 | Compliance and Regulatory Guidance, Quality Management
Understanding the CAPA Process for Medical Devices: Your Path to Compliance and QualityWhat is the CAPA process for Medical Devices? Defining CAPA:The Role of CAPA in the Medical Device Industry:Regulatory Requirements:Why the CAPA Process for Medical Devices is...
by Jeremy Moore | Jul 30, 2024 | Quality Management
Introduction to the Core Elements of a Quality Management System (QMS)Understanding a Quality Management System (QMS)Definition: What is a Quality Management System?Importance: Why is a Quality Management System Crucial for Medical Device Companies?Scope: Industries...
by Jeremy Moore | Jul 24, 2024 | Quality Management, Compliance and Regulatory Guidance
Introduction to Quality Assurance vs Quality Control in Medical DevicesUnderstanding Quality Assurance (QA) for Medical DevicesWhat is Quality Assurance for Medical Devices?The Role of Quality Assurance in Medical DevicesKey Activities in Quality...
