13485 P-756 Validation Processes For Product
ISO 13485:2016 Procedure - Validation Processes For Product - describes the process for validation of processes for production and service provision where output cannot be verified by subsequent monitoring or measurement. Addresses the establishment of criteria for review and approval of the validation process, approval of equipment and qualification of personnel, approval and use of specific methods, procedures and instructions, requirements for records, and requirements for revalidation.
Price: US$35.00
Purpose:
Responsibilities:
- This procedure describes Management Responsibilities for the Quality Management System (QMS) at Your Company.
Responsibilities:
- Top Management is responsible for establishing the Quality Policy and reviewing it for continuing suitability.
- Top Management is responsible for Communicating the Quality Policy, the importance of meeting regulatory, statutory and customer requirements.
- Top Management is responsible for identifying the Key Processes to be included in the QMS.
- Top Management is responsible for identifying the data required for effective review of the QMS.
- Top Management is responsible for identifying the management review team.
- It is the responsibility of the management review team to schedule and conduct management review meetings in compliance with this procedure.
- The Management Representative is responsible for collecting summary reports and data from the responsible functions and for ensuring adequate employee awareness of the regulatory and customer requirements.
- The management review team members are responsible for bringing information and progress reports on action items assigned to them at previous management review meetings, information on planned changes that could affect the QMS, quality planning needs and activities and recommendations for improvements to the QMS.