Analysis of the entire process of drug export to Vietnam: qualification, registration to market access
2024年10月17日
本文全面解析了中國藥品出口和越南藥品進(jìn)口的完整流程，包括出口資質(zhì)、出口許可證申請、檢驗(yàn)檢疫、海關(guān)報關(guān)等關(guān)鍵步驟，以及越南的藥品注冊、進(jìn)口許可證申請、檢疫檢測和市場準(zhǔn)入要求，幫助外貿(mào)企業(yè)順利實(shí)現(xiàn)中越藥品貿(mào)易，確保藥品符合兩國的質(zhì)量和法規(guī)標(biāo)準(zhǔn)。
Customs classification of hearing aids
March 4, 2024
Technological hearing aids such as audiometers, hearing screeners, auditory ossicles prostheses, hearing aids and cochlear implants are guaranteed compliant circulation and application through accurate customs classification, bringing hope and convenience to the hearing impaired, and working together to create a clearer world.
UKCA certification for medical devices exported to the UK
October 23, 2023
This paper provides manufacturers with a comprehensive guide to UKCA certification for the post-Brexit medical device market, including the importance of certification, the process and key timelines.
Detailed Guidelines for Exporting Medical Devices to the UK
October 20, 2023
This article is a detailed guide for medical device products exporting to the UK market, covering all the key steps from product classification to UK registration.
Analysis of the operation process of exporting medical devices to the US market
October 18, 2023
Entering the US medical device market is a complex process involving many regulations and processes. A detailed guide for medical device companies exporting to the US market, covering FDA regulatory agencies, classification of medical devices and key steps to export.
How to export medical device products to the European market
October 18, 2023
It provides a comprehensive guide for medical devices to enter the European market, from regulatory changes to technical document preparation, to the selection and registration of EU authorized representatives, and the introduction of ISO13485 standards.
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