ISO 13485- Quality Management System for Medical Devices Manufacture
ISO13485 is a quality system standard for organizations that design, develop, produce or service medical devices. It intends to promote harmonization in the medical device industry and set a basis for quality system regulations worldwide. All requirements of ISO13485 are specific to organizations manufacturing medical devices, regardless of the type or size of the organization.

The certification of a quality management system, specifically for medical devices to ISO13485 proves advantageous, and in many cases essential, for medical companies which export their products to global markets. Some of the additional requirements relate to design controls, process controls (including environmental controls), special processes, traceability, record retention, and regulatory actions, which are more critical for the medical device industry.

Benefits of ISO13485 Certification

  • An important step in the road to Total Quality Management.
  • Ensures sustained customer satisfaction by producing, delivering services and providing support functions that meet customer's needs and expectations.
  • Increases the effectiveness and efficiency of the organization through continual improvement in systems and products' /services quality
  • Opportunities for export market
  • It increases credit in the market
  • Reduction in customer complaints
  • Increase Customer Satisfaction
  • Continually improve overall performance
  • Ability to win more business
  • Facilitates the organization to become a customer-focused organization.
  • Legal Compliance

Please feel free to contact us for ISO 13485 certification