FDA and NIST collaboration on standards development activities supporting innovation and translation of regenerative medicine products-Reference-Cited by-同舟云学术

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FDA and NIST collaboration on standards development activities supporting innovation and translation of regenerative medicine products

Published:2018-06 Issue:6 Volume:20 Page:779-784
ISSN:1465-3249
Container-title:Cytotherapy
language:en
Short-container-title:Cytotherapy

Author:

Arcidiacono Judith A.^ORCID,Bauer Steven R.,Kaplan David S.,Allocca Clare M.,Sarkar Sumona^ORCID,Lin-Gibson Sheng

Publisher

Elsevier BV

Subject

Cancer Research,Transplantation,Cell Biology,Genetics (clinical),Oncology,Immunology,Immunology and Allergy

Reference24 articles.

1. Acheiving large-scale, cost-effective, reproducible manufacturing of high-quality cells—a technology roadmap to 2025,2016

2. ARM annual report: regenerative medicine clinical and financial overview;Alliance for Regenerative Medicine,2014

3. Synergizing efforts in standards development for cellular therapies and regenerative medicine;FDA Workshop,2014

4. Strategies to acheive measurement assurance for cell therapy products;NIST Workshop,2015

5. U.S. 21st Century Cures Act. Pub.L. 114–255; 2016.

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1. Standardisation is the key to the sustained, rapid and healthy development of stem cell‐based therapy;Clinical and Translational Medicine;2024-04

2. Comparative analysis of rule elements for transportation of cell therapy products among regulations and standards;Regenerative Medicine;2023-08

3. Scientific venturing for early-stage professionals (ESPs), a key concept in the innovation ecosystem;Cytotherapy;2023-04

4. Nondestructive, Longitudinal, Three-Dimensional Cell Viability Assessment Using Oxygen Imaging;2023

5. Regulatory perspectives of combination products;Bioactive Materials;2022-04

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