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Longitudinal study of the impact of three major regulations on the Korean pharmaceutical industry in the last 30 years

BACKGROUND: The pharmaceutical industry is heavily regulated. Partly for this reason, new drugs generally take over 10 years from the product development stage to market entry. Although regulations affect the pharmaceutical industry over a long period, previous studies investigating the impact of ne...

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Autores principales: Um, Seung In, Sohn, Uy Dong, Jung, Sun-Young, You, Seung-Hun, Kim, Changone, Lee, Sora, Lee, Heesang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734354/
https://www.ncbi.nlm.nih.gov/pubmed/34991612
http://dx.doi.org/10.1186/s12961-021-00797-9
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author Um, Seung In
Sohn, Uy Dong
Jung, Sun-Young
You, Seung-Hun
Kim, Changone
Lee, Sora
Lee, Heesang
author_facet Um, Seung In
Sohn, Uy Dong
Jung, Sun-Young
You, Seung-Hun
Kim, Changone
Lee, Sora
Lee, Heesang
author_sort Um, Seung In
collection PubMed
description BACKGROUND: The pharmaceutical industry is heavily regulated. Partly for this reason, new drugs generally take over 10 years from the product development stage to market entry. Although regulations affect the pharmaceutical industry over a long period, previous studies investigating the impact of new regulatory policies have usually focused on the short period before and after implementing that policy. Therefore, the purpose of this study is to examine whether and how significantly regulatory policies affect long-term innovation in the pharmaceutical industry in Korea. METHODS: This study focused on three significant regulatory policies: the introduction of the product patent system, changes in the Good Manufacturing Practice (GMP) system, and the Drug Expenditure Rationalization Plan (DERP). The study used interrupted time series (ITS) analysis to investigate the long-term impacts of the policies before and after implementation. RESULTS: Our results show that introducing the product patent system in 1987 significantly increased the number of Korean patent applications. The effect of the revised GMP policies was also statistically significant, both before and after implementation and between pre-emptive companies and non-pre-emptive ones. However, due to the companies' negotiations with the regulatory authorities or the regulatory system that links drug approval and price evaluation, the DERP did not significantly delay new drug registration in Korea. CONCLUSION: This study showed that the policies of the product patent system, GMP policies, and DERP regulations have significantly encouraged pharmaceutical companies to strive to meet regulatory requirements and promote innovation in Korea. The study suggests that it is necessary for companies to pre-emptively respond to systemic changes in development and production strategies to deal with regulatory changes and achieve sustainable growth. Also, our study results indicate that since government policies motivate the innovative system of the pharmaceutical industry, governmental authorities, when formulating pharmaceutical policies, need to consider the impact on the long-term innovation of the industry.
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spelling pubmed-87343542022-01-07 Longitudinal study of the impact of three major regulations on the Korean pharmaceutical industry in the last 30 years Um, Seung In Sohn, Uy Dong Jung, Sun-Young You, Seung-Hun Kim, Changone Lee, Sora Lee, Heesang Health Res Policy Syst Research BACKGROUND: The pharmaceutical industry is heavily regulated. Partly for this reason, new drugs generally take over 10 years from the product development stage to market entry. Although regulations affect the pharmaceutical industry over a long period, previous studies investigating the impact of new regulatory policies have usually focused on the short period before and after implementing that policy. Therefore, the purpose of this study is to examine whether and how significantly regulatory policies affect long-term innovation in the pharmaceutical industry in Korea. METHODS: This study focused on three significant regulatory policies: the introduction of the product patent system, changes in the Good Manufacturing Practice (GMP) system, and the Drug Expenditure Rationalization Plan (DERP). The study used interrupted time series (ITS) analysis to investigate the long-term impacts of the policies before and after implementation. RESULTS: Our results show that introducing the product patent system in 1987 significantly increased the number of Korean patent applications. The effect of the revised GMP policies was also statistically significant, both before and after implementation and between pre-emptive companies and non-pre-emptive ones. However, due to the companies' negotiations with the regulatory authorities or the regulatory system that links drug approval and price evaluation, the DERP did not significantly delay new drug registration in Korea. CONCLUSION: This study showed that the policies of the product patent system, GMP policies, and DERP regulations have significantly encouraged pharmaceutical companies to strive to meet regulatory requirements and promote innovation in Korea. The study suggests that it is necessary for companies to pre-emptively respond to systemic changes in development and production strategies to deal with regulatory changes and achieve sustainable growth. Also, our study results indicate that since government policies motivate the innovative system of the pharmaceutical industry, governmental authorities, when formulating pharmaceutical policies, need to consider the impact on the long-term innovation of the industry. BioMed Central 2022-01-06 /pmc/articles/PMC8734354/ /pubmed/34991612 http://dx.doi.org/10.1186/s12961-021-00797-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Um, Seung In
Sohn, Uy Dong
Jung, Sun-Young
You, Seung-Hun
Kim, Changone
Lee, Sora
Lee, Heesang
Longitudinal study of the impact of three major regulations on the Korean pharmaceutical industry in the last 30 years
title Longitudinal study of the impact of three major regulations on the Korean pharmaceutical industry in the last 30 years
title_full Longitudinal study of the impact of three major regulations on the Korean pharmaceutical industry in the last 30 years
title_fullStr Longitudinal study of the impact of three major regulations on the Korean pharmaceutical industry in the last 30 years
title_full_unstemmed Longitudinal study of the impact of three major regulations on the Korean pharmaceutical industry in the last 30 years
title_short Longitudinal study of the impact of three major regulations on the Korean pharmaceutical industry in the last 30 years
title_sort longitudinal study of the impact of three major regulations on the korean pharmaceutical industry in the last 30 years
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734354/
https://www.ncbi.nlm.nih.gov/pubmed/34991612
http://dx.doi.org/10.1186/s12961-021-00797-9
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