ISO 13485:2016

ISO 13485 – Medical Devices Quality Management System (QMS)

Ensuring Quality and Compliance in the Medical Device Industry

ISO 13485:2016 is an internationally recognized standard developed by the International Organization for Standardization (ISO). It specifies the requirements for a quality management system (QMS) specific to the medical device industry, helping organizations demonstrate their ability to consistently provide medical devices and related services that meet customer expectations and regulatory requirements.

The standard applies to all stages of the medical device lifecycle—including design and development, production, storage, distribution, installation, and servicing. It also applies to associated services like technical support and can be implemented by suppliers or third parties involved in delivering products or quality system-related services.

Who Should Implement ISO 13485?

ISO 13485:2016 is designed for organizations of any size or type involved in:

• Manufacturing and supplying medical devices

• Offering technical or quality-related services for medical devices

• Developing and maintaining systems to ensure product safety and compliance

• Any stage of the medical device lifecycle

Why Choose ISO 13485 Certification with Accurate Global?

Partnering with Accurate Global ensures a smooth certification process backed by expert guidance. Certification demonstrates your commitment to patient safety, product reliability, and regulatory compliance—key drivers of success in the medical device sector.

Key Benefits of ISO 13485 Certification

• Demonstrates Commitment to Quality
  Establishes a structured framework for delivering safe, effective, and compliant medical devices and services.

• Regulatory Compliance
  Meets international regulatory requirements, including those aligned with the EU MDR, FDA, and other global regulations.

• Enhances Customer Confidence
  Builds trust with healthcare providers, patients, distributors, and regulators through proven quality and reliability.

• Supports Continual Improvement
  Encourages a culture of continuous process enhancement and risk-based decision-making.

• Boosts Market Access and Recognition
  Certification is internationally acknowledged, opening doors to global partnerships and market opportunities.

• Competitive Advantage
  Sets your organization apart in a highly regulated and competitive industry.

Why Work with Accurate Global?

At Accurate Global, we specialize in guiding medical device manufacturers and service providers through the ISO 13485 certification journey. Our experienced auditors and consultants provide tailored support to ensure compliance, mitigate risks, and enhance product quality—ultimately protecting patient safety and boosting your brand reputation.