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Pharmaceutical

New Beginnings, New Horizons: A Strategic Merger for Enhanced Pharmaceutical Solutions

标签: • 2025年3月12日 • 评论已关闭

 

Hangzhou, February 12, 2025 – REACH24H BaiPharm (Ruiou Baiyao (Hangzhou) Pharmaceutical Technology Co., Ltd.) and Accestra Consulting Company (Hangzho…

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2025 Regulatory Insights: Navigating Pharmaceuticals Regulations in China

标签: • 2025年1月22日 • 评论已关闭

 

As 2025 begins, industries worldwide face a rapidly evolving regulatory landscape. Emerging trends, stricter compliance requirements, and new opportun…

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A Look Back at 2023: Pharmaceutical Regulatory Updates in China

标签: • 2024年1月10日 • 评论已关闭

 

Background In 2023, China implemented a range of drug regulations, encompassing various aspects such as active pharmaceutical ingredient (API) registr…

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Understanding Regulatory Requirements for Exporting Drugs to Cambodia, Laos, and Myanmar

标签: • 2023年12月4日 • 评论已关闭

 

Background Cambodia, Laos, and Myanmar are all heavily reliant on imported pharmaceutical products. A strong economic outlook in Cambodia and the intr…

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Understanding Regulatory Requirements for Exporting Drugs to Indonesia and Vietnam

标签: • 2023年11月29日 • 评论已关闭

 

In Indonesia, Southeast Asia’s largest consumer market, and Vietnam, a country which has seen a significant rise in rates of health insurance co…

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Marketing Authorization and Regulatory Requirements for Exporting Drugs to Thailand

标签: • 2023年10月16日 • 评论已关闭

 

At about 6.6% of GDP, Thailand’s healthcare expenditure is relatively high. Accordingly, the market value of pharmaceuticals in Thailand has gro…

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Understanding China’s Medical Device Classifications for Marketing Authorization

标签: • 2023年6月29日 • 评论已关闭

 

To acquire China National Medical Products Administration (NMPA)’s marketing authorization for medical devices, companies need to file or register the…

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China Pharmacovigilance (PV) Regulation Evolution and Digital PV Solution in Practice

标签: • 2023年6月15日 • 评论已关闭

 

There have been numerous new regulations put in place since China National Medical Products Administration (NMPA) joined the International Council for…

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China CDE Q&A: Electronic Drug Application and DMF Filing

标签: • 2023年5月29日 • 评论已关闭

 

On Mar. 3, 2023, China Center for Drug Evaluation (CDE) released six Q&As on drug master file (DMF) filing (Q&A No. 1-2) and drug application’…

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China Requires Electronic Submission of Drug Registration Docs from 2023

标签: • 2023年5月29日 • 评论已关闭

 

On Jan. 1, 2023, China National Medical Products Administration (NMPA) started to require that all documents for drug registration applications, as we…

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  • Contact Us
  • REACH24H USA
    Tel:+1 703 596 8055
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  • REACH24H EU
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    Email: eu@reach24h.com
  • REACH24H UK
    Tel: +44 203 5822996
    Email: uk@reach24h.com
  • REACH24H China
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