Practical and Actionable.
Our focus is on hands-on implementation. Everything you learn is designed to be applied directly in your MedTech projects.
Online Trainings
Advance your expertise with practical online training and step-by-step guides, especially designed for MedTech professionals.
Turn knowledge into action. Start learning today.
Our Trainings and Guides
When you join one of our trainings, you're not just learning theory – you're gaining direct access to the expertise of Simon Föger, a trusted MedTech specialist with over a decade of hands-on industry experience.
Simon has successfully led complex regulatory and quality projects for both startups and global MedTech manufacturers.
As a certified ISO 13485 Lead Auditor and long-standing trainer at TÜV SÜD Academy, he combines in-depth regulatory knowledge with practical implementation skills – a combination that's rare and highly valuable.
His trainings are built to save you time, cut through complexity, and give you the clarity and confidence you need – whether you're preparing for an audit, validating a process, or setting up a compliant QMS.
With Simon as your trainer, you're not just ticking a compliance box – you're making progress where it counts.
Success Stories
Frequently
Asked
Questions
We currently offer the test method validation step-by-step guide for the following test methods:
More trainings are coming in Q4/2025.
Do you want to stay informed? Subscribe to our newsletter by entering your email address in the footer, and be the first to know when new trainings go live.
Our online trainings are tailored for professionals in the medical device industry who are responsible for quality and regulatory compliance.
This includes quality engineers, regulatory affairs specialists, process development teams, validation engineers, and QA/RA project managers.
Whether you're working in a startup, SME, or established manufacturer, our trainings provide practical, ready-to-apply knowledge to support your role and accelerate project execution.
Our online trainings are designed specifically for professionals in the medical device industry who want efficient, practical, and compliant solutions.
All content is created by experts with hands-on experience in FDA, MDR, and ISO 13485 compliance, ensuring it's not only theoretically sound but also operationally effective.
Yes, a certificate of completion is available upon request. It confirms your participation and can be used to support internal training records.
Yes, for tailored in-house trainings, please contact us directly at: office@sifo-medical.com
Contact Us
Book an Appointment
Arrange your initial call with our CEO Simon Foeger
to discuss your project and clarify all your questions.
©2025 by SIFo GmbH
Bärenweg 11, 6410 Telfs, Austria
office@sifo-medical.com