Medical Device regulatory affairs has grown in complexity to protect patients and differs from region to region. In Europe, the Medical Device Regulation (MDR) is still being phased in from the Medical Device Directive (MDD). In the US, a different set of classification and regulatory approval routes exist. Our medical device regulatory affairs training provides professionals with the skills and knowledge to navigate the regulations with efficiency.
We provide both online and classroom training courses to support medical device regulatory professionals. All courses are carefully designed to improve your regulatory performance back in the workplace. Our longer online and classroom courses include post learning implementation to help you apply your skills back in the workplace. We aim to support you as you develop your regulatory career in this evolving space.
Find a course relevant for you below. Click on a course you are interested in to learn more about the agenda, delivery format, trainer and price. If you would like to join the course you must enrol and pay through the website. If you have any questions, please message us on live chat (bottom right).
We support medical device regulatory leaders improve the technical skills and knowledge of their employees, so they are equipped to overcome challenges and meet business objectives. Working together, we design and deliver technical training courses that align with your learning requirements and business goals. For more information about how we can support your team please get in touch.
Could your regulatory or quality team benefit from any of the courses listed above? Or maybe a topic which is not highlighted? We would be happy to discuss your objectives and see how we might be able to help.