Virtual manufacturing of medical devices

Law Healthcare & Pharma Guidance

Date: 29th Nov, 2024 Source: Medicines and Healthcare products Regulatory Agency (MHRA) Country: United Kingdom Original Source

Brief

New regulations require all virtual manufacturers to maintain comprehensive technical documentation for every product bearing their brand. This documentation is necessary for products placed on the market under their name. The exact requirements and implications are not specified in the provided document. However, it emphasizes the importance of technical documentation for virtual manufacturers.

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Medicines and Healthcare products Regulatory Agency (MHRA)

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Virtual manufacturing of medical devices

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Virtual manufacturing of medical devices

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Medicines and Healthcare products Regulatory Agency (MHRA)

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