Nonclinical safety evaluation of biotechnologically derived pharmaceuticals-Reference-Cited by-同舟云学术

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Nonclinical safety evaluation of biotechnologically derived pharmaceuticals

Published:2000 Issue: Volume: Page:221-258
ISSN:1387-2656
Container-title:Biotechnology Annual Review
language:
Short-container-title:

Author:

Marguerite Dempster A

Publisher

Elsevier

Reference141 articles.

1. Biotechnologically derived medical agents The scientific basis of their regulation;Chiu,1988

2. Biologics development: A regulatory overview;Scott,1993

3. Cloning and expression of the human erythropoietin gene;Lin,1985

4. Purification of human erythropoietin;Miyake;J Biol Chem,1977

5. Issues with biotechnology products in toxicologic pathology;Terrell;Toxicol Pathol,1994

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Safety Considerations for Biologics;Methods and Principles in Medicinal Chemistry;2017-08-14

2. Systemic Route;Nanomedicines and Nanoproducts;2015-02-26

3. Nonclinical Safety Assessment of Biotechnology-Derived Products: Considerations and Challenges;The Role of the Study Director in Nonclinical Studies;2014-05-09

4. Regulatory Guidelines and their Application in the Nonclinical Evaluation of Biological Medicines;Nonclinical Development of Novel Biologics, Biosimilars, Vaccines and Specialty Biologics;2013

5. Toxicology and Adverse Drug Reactions;Stephens' Detection and Evaluation of Adverse Drug Reactions;2012-01-30

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