Regulating 3D-printed medical products-Reference-Cited by-同舟云学术

Regulating 3D-printed medical products

Published:2018-10-03 Issue:461 Volume:10 Page:
ISSN:1946-6234
Container-title:Science Translational Medicine
language:en
Short-container-title:Sci. Transl. Med.

Author:

Ricles Laura M.¹²^ORCID,Coburn James C.³^ORCID,Di Prima Matthew³^ORCID,Oh Steven S.¹^ORCID

Affiliation:

1. U.S. Food and Drug Administration, Center for Biologics Evaluation and Research, Office of Tissues and Advanced Therapies, Silver Spring, MD 20993, USA.

2. U.S. Food and Drug Administration, Office of the Commissioner, Commissioner’s Fellowship Program, Silver Spring, MD 20993, USA.

3. U.S. Food and Drug Administration, Center for Device and Radiological Health, Office of Science and Engineering Laboratories, Silver Spring, MD 20993, USA.

Abstract

There are a number of key considerations in the U.S. regulatory landscape regarding approval of 3D-printed medical devices and biologics.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

Reference30 articles.

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3. 3D Bioprinting Market by Technology (Microextrusion Inkjet Laser Magnetic) Material (Cells Hydrogels Extracellular Matrices Biomaterials) Application (Clinical (Bone Cartilage Skin) & Research (Regenerative Medicine))—Global Forecasts to 2021 (Markets and Markets 2016).

4. Review: Bioprinting: A Beginning

5. Bioresorbable Airway Splint Created with a Three-Dimensional Printer

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