ISO 13485 represents the medical device industry's quality management system (QMS) standard. It specifies requirements for an organization to design and implement a QMS that can consistently meet customer and applicable regulatory requirements.

Familiarize yourself with ISO 13485 and understand how to implement it and/or audit your QMS through our courses and qualifications.

Learn in a way that works for you, whether that's live online, in person, or self-paced with on-demand eLearning.

ISO 13485 training benefits

Our courses are designed to give learners the knowledge and skill  needed to add more value to an organization, whilst developing their career. 

  • Raise internal standards and embed best practice. 
  • Achieve formal learning recognition with a BSI qualification. 
  • Grow confidence by filling gaps in knowledge. 
  • Access flexible learning in a format that works for you. 

Medical Devices Regulation Qualifications

2 stages for Medical Devices Regulation (MDR) qualification journey. 

  • Medical Devices Regulations Practitioner
  • Medical Devices Regulations Professional
  • EU MDR QMS Internal Auditor Practitioner
  • EU MDR QMS Lead Auditor Practitioner

Talk to our training advisor to guide you through the training journey. 

Funding is available for this SSG-approved course. Ask us about our early bird discount.

Phone: +65 6270 0777
Email: info.sg@bsigroup.com

 

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