Literature DB >> 23507587

[Post-marketing drug safety-risk management plan(RMP)].

Asami Ezaki1, Akiko Hori.   

Abstract

The Guidance for Risk Management Plan(RMP)was released by the Ministry of Health, Labour and Welfare in April 2012. The RMP consists of safety specifications, pharmacovigilance plans and risk minimization action plans. In this paper, we outline post-marketing drug safety operations in PMDA and the RMP, with examples of some anticancer drugs.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23507587

Source DB:  PubMed          Journal:  Gan To Kagaku Ryoho        ISSN: 0385-0684


  1 in total

1.  Japanese Physicians' Views on Drug Post-Marketing Surveillance.

Authors:  Kazuki Maeda; Rumi Katashima; Keisuke Ishizawa; Hiroaki Yanagawa
Journal:  J Clin Med Res       Date:  2015-10-23
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.