External training courses

With Medace’s biotech and medtech training courses you gain expertise on a wide range of quality, regulatory and experimental topics related to Medical Device and Advanced Therapy Medicinal Product (ATMP) development. Ranging from MDR training to Safe Aseptic Handling Techniques in an actual cleanroom environment. On this page you can find the calendar for upcoming trainings and register right away or contact us for more information.

Although we offer several courses for different levels of experience we can tailor our training to your company or research group. Most training courses are currently on request for external parties to make sure we can offer a tailored experience. Do not hesitate to contact us to get more information.

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Training calendar

MDR training

MDR & QMS Training


This full-day training workshop is a great introduction to Medical Device Regulation and Quality Management System requirements according to EN ISO 13485:2016. This will help you gain in-depth knowledge on key topics, supporting your current or future development. Take a look at the detailed agenda.


GMP Introduction training

on request

Introduction to Good Manufacturing Practice (GMP) to get to know the importance of process flows and structures within clinical development. Including hands-on information on key topics and focus areas within the Guidelines. Can be easily combined with Introduction to Quality Management for less-experienced.

MDR Training

on request

Introduction training to newly implemented Medical Device Regulation (MDR). Including the requirements for Manufacturers on Technical Documentation, Clinical Evaluation & PMS. Also exploring the classification of Medical Devices and associated rules.

biotech and medtech Training, Medace

Introduction to Quality Management

on request

Introduction to Quality Management for people to advance into Quality roles. This training covers essential elements and case examples of Quality Management in the field of medical development. Next to this, it provides practical knowhow and tools to start implementing Quality practices into your development.

Cell Culture Medace

Biological Safety

on request

In-depth multi-faceted training on Biological Safety and the role and responsibilities of Bio Safety Officers. This training highlights the steps required to set up the necessary documentation, processes and facilities to allow for biological R&D activities to take place safely. Providing useful tools and templates to implement these practices. (focused on EU and NL regulation).

cleanroom work, cleanroom clothing

Safe Aseptic Handling Techniques

on request

A full-day training on clean behavior and aseptic techniques. The training includes background information regarding regulations, contamination sources, and impact on the final product. The training consists of a classroom and a practical training at the Medace facility.

About Medace

Medace supports academic groups and companies with innovative medical concepts in need of technical, quality and clinical expertise. Bringing along a broad network, we help you to successfully develop your product into the clinical phase. With our proven pick-and-choose concept we provide you clinical product development compliant with the latest ISO and GMP standards. The biotech and medtech training courses are made available to external parties to support as many as possible innovations.

Our specialists work together with you and your team in a fully equipped and state of the art biomedical co-working space – whenever it suits you. More about Medace.