HFdocs
Effortlessly plan, document, and manage usability programs for medical devices with HFdocs—your all-in-one compliance assistant. Reduce manual effort, ensure regulatory alignment, and accelerate your development process with AI-powered documentation.
Automated Reports
HFdocs automates the generation of complex Human Factors reports, ensuring compliance with FDA and international standards. Save hours of manual work with just a few clicks, reducing the risk of errors and ensuring consistency.
Compliance Made Easy
Our built-in compliance engine helps you stay up to date with both local and international Human Factors requirements. Avoid the headache of regulatory research. HFdocs ensures your reports are always aligned with the latest standards.
Save time and cost
Traditional documentation preparation can take up to 9 weeks and cost tens of thousands of euros. HFdocs gets it done in a single day for just €300/month, giving you more time to focus on innovation instead of paperwork.
Data security and privacy
HFdocs ensures that your data is encrypted during transmission and at rest, utilizing secure protocols to protect your information. Since no sensitive or privileged data is required to generate reports, the risk is minimized while keeping the process simple and secure. Trust in a system built with privacy and security at its core.
Guided workflow for all skills levels
Training an experienced Human Factors (HF) professional can be costly and time-consuming. HFdocs eliminates that need by guiding you step by step through the process. Whether you’re a beginner or an expert, our intuitive system makes it easy, convenient, and affordable—saving you the cost of hiring a senior HF researcher.
Seamless integration
Download documents in Word format for easy updates or convert them to PDFs for seamless integration with any Quality Management System (QMS). No privileged information is required—our system generates documentation based on simple user instructions while keeping all your data secure and protected.