A Fortune 500 medical technologies firm wanted to increase the production capacity for its products. The intention was to increase capacity with a new production line that was also prepared for future products to be added to the line with minimal changes. This plan saw the addition of a new SCADA controlled production line with complex equipment integration to be used in future expansions.
Performance Validation was contracted by the medical device manufacturer to assess the quality system requirements, develop, and execute the deliverables required to validate the new production line. These deliverables include:
Performance Validation was contracted while the process was being developed and was able to assist in project scheduling and timelines.
Performance Validation was able to deliver the Validation Final Report, releasing the equipment for production on schedule and under budget. All validation deliverables fully met the medical device manufacturer’s quality requirements and will be used as a template for future validation for product launch.
The completion of validation requirements for this production line allowed for additional production capacity for current products with an easily expanded product list. Future products will be able to use the qualified equipment and SCADA system to produce quality products for the consumer without an overhaul of the current production line, which will minimize line shutdown time.
The Performance Validation team was able to leverage knowledge of ISO 13485: Medical Devices and 21 CFR 820: Quality System Regulation to ensure all regulatory requirements were met. The PV team was able to leverage knowledge and prior experience with the client’s own quality system and key personnel to anticipate the client’s expectations for documentation processes and acceptance (i.e. validation planning, document development, routing, approval, and reporting) with minimal client resource effort.
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Performance Validation is a 100% employee-owned company serving the life science industries since 1988, and is a nationwide leader in providing validation, commissioning, and quality services for pharmaceutical, biotechnology, and medical device validation for a steam autoclave manufacturers.
We are not a virtual company, a staffing agency, or a “body shop.” Our projects are managed and staffed by our own employees. We live by our Mission, which is to provide our clients with peace of mind, and we have been doing so for more than 30 years.
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Vice President, Michigan Division Director
Performance Validation, Inc