SharePoint & Power Platform Custom Solutions
Fully Tailored & Compliant Solution
Optimize and automate your Quality Management System with a tailored, compliant solution built on PowerApps, SharePoint, and Power Automate. Ensure full data control, seamless integration, and regulatory compliance with ISO 13485, ISO 9001, and FDA 21 CFR Part 11, eliminating manual work and vendor lock-in while enhancing transparency and efficiency.
Transform your Quality Management System (QMS) with a fully customized solution built on Microsoft SharePoint, Power Apps, and Power Automate. Say goodbye to manual inefficiencies and paper-based documentation, and embrace a smarter, faster, and fully compliant way to manage processes, approvals, and records.
Medical Device Regulation
Efficacy and feasibility is as important as compliance
Real-World Solution for Your Organization
We understand the regulatory environment. We have experience in implementing all standards related to medical software development, cybersecurity, and technical documentation, and we would be happy to demonstrate in practice how we can translate this expertise into real-world solutions while working on your medical device software product - as a developers a project managers.
Medical Device Software Development (SaMD/MDSW)
Medical Device Software Development
- Software Development
- Technical Documentation
- Medical Project Management
- Regulatory Compliance
Quality Management Digitalization
and Automation for ISO 13485
Future of Quality Management
At QMLogic, we empower organizations to revolutionize their Quality Management Systems (QMS) with cutting-edge automation tools. Our expertise spans Microsoft SharePoint, Power Platform, Confluence, Jira, and custom-built solutions tailored to specific needs.
