Quality Training

Training

Accelerate Time to Market

Maintaining an effective and compliant quality management system (QMS) in the MedTech and IVD industry is more than a regulatory requirement, it’s essential for product safety, patient trust, and business success. Yet many companies struggle to keep pace with evolving expectations from global regulators and implementing those requirements into their QMS effectively.

Qserve Learn provides quality related training designed by active industry experts who understand the real-world challenges of medical device and IVD design, manufacturing and quality assurance. Whether you're building a QMS from scratch or optimizing an existing one, our training gives your teams the learning tools and confidence to improve processes, reduce risk, and meet regulatory expectations with ease.

We offer training in multiple formats [virtual, in-company, e-learning, webinars, and on-demand] so your team can learn in the way that works best, anytime, anywhere.

Our Training Courses

These best-selling training courses in the area of Quality Assurance are trusted by QA and RA professionals to meet quality requirements and drive operational excellence:

ISO 13485:2016 Implementation

Learn how to implement, maintain, and audit a QMS aligned with global medical device expectations.

Internal Auditing for Medical Devices and IVD’s

Gain the skills to plan, execute, and report internal audits that add real value and ensure compliance.

Supplier Quality Management

Understand how to qualify, monitor, and manage suppliers as part of your QMS and risk management strategy.

Complaint Handling & Vigilance Reporting

Learn how to process complaints efficiently and comply with post-market reporting requirements.

Basics of Risk Management (ISO 14971)

For starters in the sector, this is an essential course that is key to all aspects of design, manufacture and distribution of medical devices and IVD’s.

Design Transfer

An in-depth training with practical examples and learning from common pitfalls on transferring medical devices and IVD’s from finished designs to production successfully.

server render fail/waiting for island-7f870ei1R0 (separate island render, inside)

FAQ

Frequently Asked Questions About Quality Training Topics

Still have questions? We are here to help, including quality training topics.

Qserve Learn offers instructor-led virtual training, in-company sessions, self-paced e-learning, and recorded webinars covering the full range of medical device quality topics.

These courses are ideal for quality assurance professionals, regulatory managers, auditors, production leads, and anyone involved in maintaining or improving a QMS. To ensure relevance and impact, each training is available at a beginner, intermediate, or advanced level, depending on your team's knowledge and responsibilities.

Yes, all our quality training content is aligned with ISO 13485, ISO 14971, FDA QSRs, and relevant regional regulations to ensure practical, up-to-date guidance.

Absolutely. Our in-company training options can be fully customized to your existing processes, challenges, and device types. Feel free to reach out for more information and a personal offer.

All content is developed and delivered by Qserve consultants who work daily with manufacturers and notified bodies, ensuring it reflects current best practices and compliance expectations.

Services Areas

Solutions

Expertise

Resource Center

About us

Careers

Quality Training for the Medical Device and IVD Industry

Accelerate Time to Market

These best-selling training courses in the area of Quality Assurance are trusted by QA and RA professionals to meet quality requirements and drive operational excellence:

ISO 13485:2016 Implementation

Internal Auditing for Medical Devices and IVD’s

Supplier Quality Management

Complaint Handling & Vigilance Reporting

Basics of Risk Management (ISO 14971)

Design Transfer

Stay Proactive with Quality Compliance

Explore our training calendar to find sessions that match your quality role, device type, and region. New topics are added regularly based on industry trends and regulatory updates.

Stay Proactive with Quality Compliance

Still have questions? We are here to help, including quality training topics.

Quality Training for the Medical Device and IVD Industry

Accelerate Time to Market

These best-selling training courses in the area of Quality Assurance are trusted by QA and RA professionals to meet quality requirements and drive operational excellence:

ISO 13485:2016 Implementation

Internal Auditing for Medical Devices and IVD’s

Supplier Quality Management

Complaint Handling & Vigilance Reporting

Basics of Risk Management (ISO 14971)

Design Transfer

Stay Proactive with Quality Compliance Explore our training calendar to find sessions that match your quality role, device type, and region. New topics are added regularly based on industry trends and regulatory updates.

Stay Proactive with Quality Compliance

Still have questions? We are here to help, including quality training topics.

Stay Proactive with Quality Compliance

Explore our training calendar to find sessions that match your quality role, device type, and region. New topics are added regularly based on industry trends and regulatory updates.