Literature DB >> 21326288

The value and benefits of the International Conference on Harmonisation to drug regulatory authorities: advancing harmonization for better public health.

J A Molzon1, A Giaquinto, L Lindstrom, T Tominaga, M Ward, P Doerr, L Hunt, L Rago.   

Abstract

The International Conference on Harmonisation (ICH) is an unparalleled undertaking, which has brought together drug regulatory authorities and pharmaceutical trade associations from Europe, Japan, and the United States, to discuss the scientific and technical aspects of medical product registration. Launched in 1990, the value and benefits of ICH to regulators are being realized. ICH has harmonized submission requirements and created a harmonized submission format that is relieving both companies and regulatory authorities of the burdens of assembling and reviewing separate submissions for each region. As more countries embrace ICH guidelines, we anticipate additional benefits, including the promotion of good review practices and, ultimately, a common regulatory language that will facilitate further interactions among global drug regulatory authorities.

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Year:  2011        PMID: 21326288     DOI: 10.1038/clpt.2011.10

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  14 in total

1.  Overwhelmed drug regulators seek cure in cooperation.

Authors:  Lucas Laursen
Journal:  Nat Med       Date:  2011-07-07       Impact factor: 53.440

2.  Recent trends for drug lag in clinical development of oncology drugs in Japan: does the oncology drug lag still exist in Japan?

Authors:  Hideki Maeda; Tatsuo Kurokawa
Journal:  Int J Clin Oncol       Date:  2015-04-03       Impact factor: 3.402

3.  Be open about drug failures to speed up research.

Authors:  Enrica Alteri; Lorenzo Guizzaro
Journal:  Nature       Date:  2018-11       Impact factor: 49.962

4.  Enhancing the work of the Department of Health and Human Services national vaccine program in global immunization: recommendations of the National Vaccine Advisory Committee: approved by the National Vaccine Advisory Committee on September 12, 2013.

Authors: 
Journal:  Public Health Rep       Date:  2014       Impact factor: 2.792

5.  Differences in maximum tolerated doses and approval doses of molecularly targeted oncology drug between Japan and Western countries.

Authors:  Hideki Maeda; Tatsuo Kurokawa
Journal:  Invest New Drugs       Date:  2014-03-11       Impact factor: 3.850

6.  The Global academic research organization network: Data sharing to cure diseases and enable learning health systems.

Authors:  Masanori Fukushima; Christopher Austin; Norihiro Sato; Tatsuya Maruyama; Eileen Navarro; Mitra Rocca; Jacques Demotes; Melissa Haendel; Samuel L Volchenboum; Matthew Cowperthwaite; Jonathan C Silverstein; Chris Webb; Ida Sim; Marianne Chase; John Speakman; Erika Augustine; Daniel E Ford; Rebecca Kush
Journal:  Learn Health Syst       Date:  2018-12-03

7.  Impact of regulatory requirements on medicine registration in African countries - perceptions and experiences of pharmaceutical companies in South Africa.

Authors:  Kirti Narsai; Abeda Williams; Aukje Kaija Mantel-Teeuwisse
Journal:  South Med Rev       Date:  2012-07-23

8.  The views of healthcare professionals, drug developers and regulators on information about older people needed for rational drug prescription.

Authors:  Erna Beers; Toine C G Egberts; Hubert G M Leufkens; Paul A F Jansen
Journal:  PLoS One       Date:  2013-08-16       Impact factor: 3.240

9.  Clinical study reports of randomised controlled trials: an exploratory review of previously confidential industry reports.

Authors:  Peter Doshi; Tom Jefferson
Journal:  BMJ Open       Date:  2013-02-26       Impact factor: 2.692

Review 10.  Clinical studies in lysosomal storage diseases: Past, present, and future.

Authors:  Pol F Boudes
Journal:  Rare Dis       Date:  2013-10-07
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