Hurdles of environmental risk assessment procedures for advanced therapy medicinal products: comparison between the European Union and the United States-Reference-Cited by-同舟云学术

Hurdles of environmental risk assessment procedures for advanced therapy medicinal products: comparison between the European Union and the United States

Published:2019-08-09 Issue:7 Volume:49 Page:580-596
ISSN:1040-8444
Container-title:Critical Reviews in Toxicology
language:en
Short-container-title:Critical Reviews in Toxicology

Author:

Iglesias-Lopez C.¹,Obach M.²,Vallano A.¹²,Agustí A.¹³,Montané J.⁴^ORCID

Affiliation:

1. Department of Pharmacology, Therapeutics and Toxicology, Universitat Auntònoma de Barcelona, Barcelona, Spain;

2. Medicines Department, Catalan Healthcare Service, Barcelona, Spain;

3. Clinical Pharmacology Service, Vall d’Hebron University Hospital, Barcelona, Spain;

4. Blanquerna School of Health Science, Ramon Llull University, Barcelona, Spain

Publisher

Informa UK Limited

Subject

Toxicology

Link

https://www.tandfonline.com/doi/pdf/10.1080/10408444.2019.1689380

Reference11 articles.

1. Environmental risk assessment for medicinal products containing genetically modified organisms

2. Chimeric Antigen Receptor-T Cell Therapy

3. CRISPR plants now subject to tough GM laws in European Union

4. Regulatory Framework for Advanced Therapy Medicinal Products in Europe and United States

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