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Regulatory Considerations in the Design and Manufacturing of Implantable 3D‐Printed Medical Devices

https://doi.org/10.1111/cts.12315
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23/23 checkable references clean · checked 2026-07-22

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

16 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 23 checked references that resolve
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no DOI — not checkedU.S. Department of Health and Human Services: Requests for Feedback on Medical Device submissions: the Pre‐Submission Program and Meetings with Food and Drug Administration.Guidance for Industry and Food and Drug Administration Staff.http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/UCM311176.pdf. Issued February 18 2014. Accessed October 1 2014.
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