Equip is our training provision service. We organise and run an increasing range of training courses which are carefully designed to equip medical device manufacturers with the knowledge and expertise they need to effectively fulfil their respective role. Whether you are an internal auditor looking to refresh knowledge of auditing techniques, a Quality specialist taking on PRRC responsibilities under an MDR 2017/745 complaint process, or a manufacturer wishing to understand the fundamentals of Adverse event and Advisory Notice reporting requirements as they apply in Canada, Japan or the USA. We have courses to help your organisation confidently fulfil quality and regulatory requirements.

Book an upcoming MedRAS Equip course