Regulatory and Ethical Considerations
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Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-97-5906-4_11
Reference16 articles.
1. Oberweis CV, Marchal JA, López-Ruiz E, Gálvez-Martín P (2020) A worldwide overview of regulatory frameworks for tissue-based products. Tissue Eng. Part B, Rev 26(2):181–196. https://doi.org/10.1089/ten.TEB.2019.0315
2. Suhag D, Kaushik S, Taxak VB (2024) Introduction to Biomedical Materials. In: Handbook of Biomaterials for Medical Applications, Volume 1. Biomedical Materials for Multi-functional Applications. Springer, Singapore. https://doi.org/10.1007/978-981-97-4818-1_1
3. Greenspan DC, Hench LL (2005) Regulatory classification of biomaterials and medical devices. In Elsevier eBooks (pp. 251–257). https://doi.org/10.1533/9781845690861.5.251
4. Alas JK, Godlovitch G, Mohan CM, Jelinski SA, Khan AA (2017) Regulatory framework for conducting clinical research in Canada. Can J Neurol Sci. Le journal canadien des sciences neurologiques 44(5):469–474. https://doi.org/10.1017/cjn.2011.458
5. Wang S (2015) Formulations in paediatric investigation plans (PIPs): introduction to PIP quality section and regulatory framework. Int J Pharm 492(1–2):332–334. https://doi.org/10.1011/j.ijpharm.2015.05.011
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