A review of clinical pharmacology deficiencies of European centralised drug marketing authorisation applications-Reference-Cited by-同舟云学术

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A review of clinical pharmacology deficiencies of European centralised drug marketing authorisation applications

Published:2020-12 Issue: Volume:118 Page:104804
ISSN:0273-2300
Container-title:Regulatory Toxicology and Pharmacology
language:en
Short-container-title:Regulatory Toxicology and Pharmacology

Author:

Hay Justin L.^ORCID,O'Sullivan Jane,Kerwash Essam^ORCID,Ilie Alexandra-Roxana,Cole Susan M.

Funder

Horizon 2020 Marie Sklodowska-Curie

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference15 articles.

1. Regulatory issues for orphan medicines: a review;Bouwman;Health Pol. Technol.,2020

2. An analysis of marketing authorisation applications via the mutual recognition and decentralised procedures in Europe;Ebbers;Eur. J. Clin. Pharmacol.,2015

3. Survey 2008 on the Performance of EMEA Scientific Procedures for Medicinal Products for Human Use,2009

4. European Medicines Agency Annual Report 2018,2018

5. Guideline on Evaluation of Medicinal Products Indicated for Treatment of Bacterial Infections,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

1. Off-label and unlicensed drug treatments in Neonatal Intensive Care Units: a systematic review;J PEDIATR NEONATAL I;2021

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