Author:
Rajpoot Kuldeep,More Anand,Wankhede Yogesh,Gomte Shyam,Tekade Muktika,Gupta Tanisha,Pawar Bhakti,Gandhi Sanyam,Tekade Rakesh Kumar
Reference60 articles.
1. Determination of the Appropriate FQPA Safety;Assessment,2002
2. An FDA/CDER perspective on non-clinical testing strategies: classical toxicology approaches and new approach methodologies (NAMs);Avila;Regul. Toxicol. Pharmacol.,2020
3. Validating and troubleshooting ocular in vitro toxicology tests;Barile;J. Pharmacol. Toxicol. Methods,2010
4. Toxicological evaluation of biotechnology products: a regulatory viewpoint;Bass,1987
5. Identification of regulatory needs for nanomedicines;Bremer-Hoffmann;J. Interdisc. Nanomed.,2018
Cited by
1 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