Skip to content
Cart

Training for Medical Device Sector: EU MDR for Importers and Distributors, ISO 13485, ISO 17025 & Internal Quality Audits.


All training is delivered through our training partner  SQT Training Ltd. Participation in the NSAI TC005 Healthcare Standards Committee facilitates an early understanding of upcoming changes to standards and an opportunity to collaborate with peers to shape international best practice.  

The training courses below were designed by Limehill Quality Solutions over the last 6 years to address specific industry training needs arising from new or revised standards and regulations.  The majority of training provided is customised to reflect the use of clients' documentation and data.  Public courses are also available.  Clients are supported with training onsite/remotely in the following topics, and further information on course brochures and client reviews can be accessed on the SQT website at the links below:

Regulatory Requirements for Importers and Distributors of Medical Devices EU MDR 2017/745

Interpretation and Understanding of Test Results from Testing Laboratories

Demystifying Calibration Certificates: How to Interpret and Understand 

The following courses are also delivered through SQT Training Ltd. on behalf of Micromatters: 

Internal Quality Auditing Course for Manufacturers of Medical Devices

ISO 13485: 2016

Good Laboratory Practice QMS ISO 17025 Requirements