Online & Blended Medical Devices Quality/Regulatory Training Courses
Comply Guru™ is offering online, virtual & blended Medical Devices (Quality Assurance & Regulatory Affairs) Training Courses including ISO 13485:2016, EU Medical Device Regulation (MDR), Risk & ISO 14971:2019, MD SAP & more.
ISO 13485:2016 is a Quality Management System Standard which outlines the requirements for regulatory purposes. These requirements are intended to be applicable to any medical device organisation regardless of size and activity as a basis for demonstrating and supporting compliance with applicable regulatory requirements.
The European Medical Device Regulation (MDR) is a set of regulations that must be met if producing or distributing medical devices within the EU, and if you want to sell your Medical Devices in the EU. Comply Guru have partnered with Meddev Solutions UK to develop online & self-paced courses on the EU MDR which are now available!
Request a free demo today to see if our training is for you!
FILTER BY STANDARD OR REGULATION
Filter By Course Type
Filter By Product Type
This online course will offer an interactive overview of Clinical Evaluation for Medical Devices & MEDDEV 2.7/1.
Some Companies that have used Comply Guru™
The Numbers - How We Are Doing
Our Pass Rate
Would Recommend Comply Guru
Gave us 4/5 Stars or higher Overall Training Experience
Would Recommend Online or Blended Training over Classroom Training
Want to learn more? Get in touch.
Would you like to know more about our service? We have a dedicated sales team who would be happy to answer any questions that you may have.
Standards Simplified. Training Transformed.
Our mission is to simplify the complex world of Standards, combine leading subject matter experts, graphic & instructional designers & technology together so our Learners benefit from all of the advantages that the best in online Learning can offer anywhere!Join Our Newsletter