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| Information about US FDA 21 CFR 820.30 - https://operonstrategist.com/services/regulatory-approvals/design-and-development-documentation/us-fda21-cfr820-30/?utm_source=Article%20Submission&utm_medium=Off%20page1&utm_campaign=Article%20Submission Operon Strategist the leading medical device regulatory consultant providing consultation for 21 CFR 820.30 design control with extensive experience and the practical implementation of design controls regulation for developing new design control processes or for making improvements to existing processes. We assist in design controls as per FDA and ISO 13485:2016 that can be mapped to the process that works best for the organization and the product being developed. If you need any help setting up a design control system, or wish to modify an existing system in order to align with ISO 13485 or FDA design controls, please contact us. »» Details for Information about US FDA 21 CFR 820.30 |
