Regulatory science for biomaterials: are we doing right things right? Abstract

Glavni sadržaj članka

Michael Gasik
https://orcid.org/0000-0002-5782-7987

Apstrakt

The aim of this work is to highlight gaps and drawbacks in modern development of biomaterials which are intended themselves alone or in combination to be deployed in medical devices, especially for Class III under the EU MDR 2017/745. More tight requirements for biomaterials safety and efficacy demand proper testing and assessment which might be not always aligned with the R&D process.

Detalji članka

Rubrika

Biomaterials for orthopedic and dental applications

Kako citirati

[1]
M. . Gasik, “Regulatory science for biomaterials: are we doing right things right? Abstract”, Hem Ind, vol. 78, no. 1S, p. 32, Mar. 2024, Accessed: Dec. 22, 2024. [Online]. Available: https://www.ache-pub.org.rs/index.php/HemInd/article/view/1275

Funding data

Reference

Gasik M. Understanding biomaterial-tissue interface quality: combined in vitro evaluation. Sci. Techn. Adv. Mater. (2017), 18:550-562. https://doi.org/10.1080%2F14686996.2017.1348872

Zuhlke A. Dynamic mechanical characterization of biomaterials for medical devices. Aalto University Doctoral Theses (2023), 148 p. https://urn.fi/URN:ISBN:978-952-64-1255-9

Gasik M. Biomechanical characterization of engineered tissues and implants for tissue/organ replacement applications. In: Biomaterials for Organ and Tissue Regeneration, Eds. E.N. Vrana, H. Knopf-Marques, J. Barthes, Woodhead Publ. (2020), 599-627. https://shop.elsevier.com/books/biomaterials-for-organ-and-tissue-regeneration/vrana/978-0-08-102906-0

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