Accelerate Your Quality Assurance Validation Process
Medical device quality assurance relies heavily on validation, which is necessary to meet FDA requirements. Be that as it may, clinical gadget producers new to CMMs aren’t generally certain how to accomplish FDA consistency. Without creating production bottlenecks, how can you shorten the integration time of your new quality assurance system?
ZEISS Modern Quality Arrangements has laid out rules and approval techniques from broad examination to agree with FDA guidelines, including 21 CFR Section 11 and 21 CFR 820. Through our full scope of administrations, we offer help to approve ZEISS CMMs and the whole review process.
You can choose from multiple options:
- Free 1-hour eLearning – Learn best practices and methods used in the regulatory industry to validate CMM systems and the inspection process
- CMM validation solution for FDA compliance – ZEISS provides detailed instructions and support for validation in accordance with FDA regulatory requirements
- ZEISS OEM package for FDA compliance – ZEISS provides authorized use of validation protocols and documentation for a specific CMM system
Do you need more information about ZEISS CMM Validation Services?
Fill out the form to download our flyer, “Accelerate Your Quality Assurance Validation Process: ZEISS CMM Validation Service.” to get a deep dive into the many benefits of our offerings, including saving time and gaining in-depth consultation.
You can also choose to have one of our expert team members contact you to discuss your quality assurance validation challenges and needs.
