MEDQURE
Courses and Consultancy

  COURSES & CONSULTANCY


Get up to speed with the latest medical device standards and regulations.

Browse the courses and consultancy we can offer you at your location.

Available to medtech companies throughout the EU.



2020


The NEW MDR                                         Medical Device Regulations

The new rules are covered in two days of intensive training covering the entire MDR and some MDD. Tailored to your product group.


Add a day of consultancy for support and implementation.



2020


Usability Engineering EN62366-1


A popular course for companies taking a user centric approach to design and development. Tailored to your product group.


Add a day of consultancy for support and implementation.



2020


Clinical Evaluation & Post Market Surveillance

The new guidance and MDR are driving the clinical process. Learn what you need to know here and how it affects your products.


Add a day of consultancy for support and implementation


2020


Biocompatibility - A Risk Based Approach


A thorough  1 day course on biocompatibility assessments, risk based plans etc.


Add a day or two of consultancy for additional support and implementation.


2020


Software & Apps


Is  your app a medical device? Ensure your software and apps meet the latest FDA & EU requirements with this in-depth 1 day course.


Add a day or two of consultancy for additional support and implementation.


2020


Quality Management for Medical Devices & ISO 13485

A course that is relevant for anyone working in medical device development.


Add a day of consultancy for additional support and implementation.



2020


Risk Management for Medical Devices & ISO 14971


The 2 day course will give you the knowledge to complete a medical device risk management file and more.



2020


Unique Device Identification UDI

A popular course for companies taking a user centric approach to design and development. Tailored to your product group.


Add a day of consultancy for additional support and implementation.


2020


Additional training and consultancy in

  • Electrical IVD Devices EN61010
  • Electrical Medical Devices EN60601
  • ROHS Restrictions of Hazardous Devices
  • The New IvDR
  • 13485 Quality System Internal Audit