Analysis of the entire process of drug export to Vietnam: qualification, registration to market access
17 October 2024
This article comprehensively analyzes the complete process of Chinese drug exports and Vietnamese drug imports, including export qualification, export license application, inspection and vaccination, customs clearance and other key steps, as well as Vietnams drug registration, import license application, vaccination testing and market access requirements, to help foreign trade enterprises to smoothly Sino-Vietnamese drug trade and ensure that the drugs meet the quality and regulatory standards of the two countries.
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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