ISO 13485 Training Courses on Medical Device Quality Management Systems (MD-QMS)

Comply Guru are the first in the world to offer Multi-Accredited ISO 13485 Training with the Chartered Quality Institute (CQI), International Registrar of Certificated Auditors (IRCA) and the Regulatory Affairs Professionals Society (RAPS) offering credentials for the Medical Device Industry that are globally recognized.

ISO 13485 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. ISO 13485 can also be used by suppliers or external parties that provide products, including quality management system-related services to such organizations.

Comply Guru offer different types of ISO 13485 training courses depending on the target audience and training needs. We can also tailor training to meet your company’s specific needs or requirements. Our courses are available in multiple formats from eLearning, Blended Learning or Instructor-led Learning to help you or your organization master Medical Device Quality Management Systems (MD-QMS) for Regulatory Purposes.