Design Transfer Procedure | ISO 13485 | FDA QSR Compliant
- ISO 13485:2016 Compliant
- FDA QSR Compliant
- Includes Detailed Forms
- MS Word Format
- Digital Content - Instant Download
Design Transfer ProcedureThe Design Transfer Procedure provides instruction on the transfer of medical devices from design and development to manufacturing.
Design Transfer Procedure - OverviewThe Design Transfer Procedure ensures the product and processes have been properly transferred prior to the commercial release of a medical device. The Design Transfer Procedure governs the transfer of a medical device product and related processes from the development phase to manufacturing in advance of product launch and commercialization.
Design Transfer Procedure ComplianceThe Design Transfer Procedure is FDA 21 CFR Part 820 and ISO 13485:2016 compliant.
To learn more about our Design Transfer Procedure contact us at [email protected]
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ISO 13485 Design Transfer Procedure
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