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ISO 13485 2003

TRANSLATED INTO PLAIN ENGLISH

ISO 13485 is a Quality Management Standard for Medical Devices

 

ISO 13485 2003 IN PLAIN ENGLISH


ISO 13485 2003 MEDICAL DEVICE STANDARD IN PLAIN ENGLISH

ISO 13485

4. Systemic Requirements

4.1
Establish
a quality  system for medical devices

 

Develop a quality management system for medical devices.

  • Identify the processes that make up your quality system.

  • Describe your quality management processes.

Implement a quality management system for medical devices.

  • Use quality system processes.

  • Control process performance.

 

Maintain your medical device quality management system.

  • Monitor the effectiveness of your processes.

  • Maintain the effectiveness of your processes.

4.2
Document your medical device quality system

4.2.1 Develop quality management system documents.

  • Develop documents to implement your quality system.

  • Develop a file for each model or type of medical device.

  • Develop a file for each type of related service.

 

4.2.2 Prepare quality management system manual.

  • Document your procedures.

  • Describe how your processes interact.

  • Specify the scope of your quality system.

  • Justify exclusions and reductions in scope.

  • Describe how your documentation is structured.

 

4.2.3 Control quality management system documents.

  • Approve documents before you distribute them.

  • Provide the correct version of documents at points of use.

  • Review and re-approve documents when you update them.

  • Specify the current revision status of your documents.

  • Monitor documents that come from external sources.

  • Prevent the accidental use of obsolete documents.

  • Preserve the usability of your quality documents.

  • Retain obsolete documents for medical devices.

 

4.2.4 Maintain quality management system records.

  • Use your records to prove that requirements have been met.

  • Develop a procedure to control medical device records.

  • Ensure that your medical device records are useable.

  • Retain records related to medical devices.

   

ISO 13485 2003 MEDICAL DEVICE STANDARD IN PLAIN ENGLISH

ISO 13485

5. Management Requirements

5.1
Support 
quality

Promote the importance of quality.

  • Promote the need to meet customer requirements.

  • Promote the need to meet medical device requirements.

 

Develop a quality management system.

  • Support the development of a quality system.

  • Formulate your organization's quality policy.

  • Set your organization's quality objectives.

  • Provide needed quality resources.

 

Implement your quality management system.

  • Provide resources to implement quality management system.

  • Encourage people to meet quality system requirements.

 

Maintain your quality management system.

  • Perform quality management reviews.

  • Provide resources to maintain quality system.

5.2
Focus on customers

Identify customer requirements.

  • Expect people to identify customer requirements.

 

Meet customers requirements.

  • Expect your organization to meet customer requirements.

5.3
Establish
a quality
policy

Define your quality policy.

  • Ensure that it serves your organization's purpose.

  • Ensure that it emphasizes the need to meet requirements.

  • Ensure that it facilitates the development of quality objectives.

  • Ensure that it makes a commitment to continuous improvement.

 

Manage your quality policy.

  • Communicate your policy throughout your organization.

  • Review your policy to ensure its continued suitability.

5.4
Perform
quality planning

5.4.1 Formulate quality objectives.

  • Ensure that objectives are set for all functional areas.

  • Ensure that objectives are set at organizational levels.

  • Ensure that objectives facilitate product realization.

  • Ensure that objectives support the quality policy.

  • Ensure that objectives are measurable.

 

5.4.2 Plan quality management system.

  • Plan the development of your quality management system.

  • Plan the implementation of your quality management system.

  • Plan the improvement of your quality management system.

  • Plan the modification of your quality management system.

5.5
Control
your quality management system

5.5.1 Define responsibilities and authorities.

  • Document responsibilities and authorities.

  • Communicate responsibilities and authorities.

  • Define how people should interact with each other.

 

5.5.2 Appoint management representative.

  • Oversee your quality management system.

  • Report on the status of your quality system.

  • Support the maintenance of your quality system.

  • Promote the importance of regulatory requirements.

 

5.5.3 Support internal communications.

  • Ensure that communication processes are established.

  • Ensure that communication occurs throughout organization.

5.6
Carry out management reviews

5.6.1 Review quality management system.

  • Plan regular reviews of your quality system.

  • Evaluate the effectiveness of your quality system.

  • Maintain a record of your management reviews.

 

5.6.2 Examine management review inputs.

  • Examine audit results.

  • Examine product conformity data.

  • Examine opportunities to improve.

  • Examine feedback from customers.

  • Examine process performance information.

  • Examine corrective and preventive actions.

  • Examine changes that might affect your system.

  • Examine changes in your regulatory requirements.

  • Examine previous quality management reviews.

 

5.6.3 Generate management review outputs.

  • Generate actions to improve maintenance of quality system.

  • Generate actions to improve your organization's products.

  • Generate actions to address your resource needs.


ISO 134852003 MEDICAL DEVICE STANDARD IN PLAIN ENGLISH

ISO 13485

6. Resource Requirements

6.1
Provide quality resources

Identify quality management system resource requirements.

  • Identify resources needed to support the quality system.

  • Identify resources needed to meet customer requirements.

  • Identify resources need to meet regulatory requirements.

 

Provide quality management system resources.

  • Provide resources needed to support the quality system.

  • Provide resources needed to implement the quality system.

  • Provide resources needed to maintain the quality system.

  • Provide resources needed to meet regulatory requirements.

6.2
Provide quality personnel

6.2.1 Use competent personnel.

  • Ensure that your personnel have the right experience.

  • Ensure that your personnel have the right education.

  • Ensure that your personnel have the right training.

  • Ensure that your personnel have the right skills.

 

6.2.2 Support competence.

  • Define acceptable levels of competence.

  • Identify your training and awareness needs.

  • Establish training needs assessment procedures.

  • Deliver your training and awareness programs.

  • Evaluate effectiveness of training and awareness.

  • Maintain a record of competence.

6.3
Provide quality infrastructure

Identify infrastructure needs.

  • Identify your building needs.

  • Identify your workspace needs.

  • Identify your hardware needs.

  • Identify your software needs.

  • Identify your utility needs.

  • Identify your equipment needs.

  • Identify your support service needs.

  • Identify your maintenance needs.

 

Provide needed infrastructure.

  • Provide needed buildings.

  • Provide needed workspaces.

  • Provide needed hardware.

  • Provide needed software.

  • Provide needed utilities.

  • Provide needed equipment.

  • Provide needed support services.

  • Provide needed maintenance services.

 

Maintain your infrastructure.

  • Maintain your buildings.

  • Maintain your workspaces.

  • Maintain your hardware.

  • Maintain your software.

  • Maintain your utilities.

  • Maintain your equipment.

  • Maintain your support services.

  • Maintain your maintenance services.

  • Maintain a record of maintenance activities.

6.4
Provide quality environment

Identify needed work environment.

  • Identify work environment for medical products.

  • Identify your organization's health requirements.

  • Identify your organization's clothing requirements.

  • Identify your organization's cleanliness requirements.

  • Identify your organization's working condition requirements.

 

Implement needed work environment.

  • Meet your organizations work environment needs.

  • Meet your organization's health requirements.

  • Meet your organization's clothing requirements.

  • Meet your organization's cleanliness requirements.

  • Meet your organization's working condition requirements.

 

Manage needed work environment.

  • Control your organization's work environment.

    • Control your organization's health practices.

    • Control your organization's clothing practices.

    • Control your organization's cleanliness practices.

  • Implement procedures to monitor working conditions.

  • Establish special arrangements for contaminated products.

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