This 10 key issue must be understood!
March 16, 2025
According to the latest international trade rules of 2025, medical device exports must meet the triple certification system: Production enterprise qualifications: ISO 13485 quality system certification, product registration certificate (such as China NMPA, US FDA 510(k)) Trade enterprise qualifications: medical device business license, import and export rights record.
How to choose a reliable chemical agent export agency? A comprehensive analysis of compliance key points in 2025
April 19, 2025
What special certifications are required for chemical exports? In 2025, chemical export agents must hold dual certifications: standard Foreign Trade Operator Registration Record and Hazardous Chemicals Business License for dangerous goods. Special categories require additional attention: Pesticides require MOA Pesticide Export Registration Release Notice...
How to become a general export agent for pharmaceuticals? These 5 core issues must be clarified!
May 8, 2025
How to choose a reliable pharmaceutical export general agent? When selecting a pharmaceutical export general agent, focus on three major certifications: Pharmaceutical Business License (must include import/export qualifications) ISO13485 Medical Device Quality Management System Certification Target market GSP/GMP compliance records (such as EU GDP certificate) It is recommended to request the agent to provide export cases of similar products in the past 3 years...
How to handle medical consumables export agency? These 8 key questions must be understood!
As a 20-year foreign trade veteran, Im often asked an interesting question: Why do seemingly similar paper products have completely different customs classifications? Today, lets uncover the identity code of household paper products like detectives solving a case.
Certification maze: No pass means no entry
How to choose an export inspection agent? What does the inspection process include? How to solve common problems?
May 30, 2025
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How can medical plastic products expand into overseas markets through agency companies? These key issues must be understood!
June 27, 2025
醫(yī)療塑料出口需要哪些特殊資質(zhì)認(rèn)證？ 根據(jù)2025年最新國(guó)際貿(mào)易規(guī)范，醫(yī)療塑料制品出口需重點(diǎn)關(guān)注三類(lèi)認(rèn)證： 基礎(chǔ)生產(chǎn)資質(zhì)：ISO13485醫(yī)療器械質(zhì)量管理體系認(rèn)證 目標(biāo)市場(chǎng)準(zhǔn)入認(rèn)證： 美國(guó)FDA 510(k)或PMA認(rèn)證 歐盟CE-MDR認(rèn)證（2020年升級(jí)版仍有...
How to become a medical equipment export agent? A comprehensive analysis of the latest compliance points for 2025.
July 13, 2025
一、醫(yī)藥器材出口需要哪些資質(zhì)認(rèn)證？ 根據(jù)2025年最新國(guó)際貿(mào)易規(guī)范，醫(yī)藥器材出口需滿(mǎn)足雙重認(rèn)證體系： 國(guó)內(nèi)強(qiáng)制資質(zhì)： 醫(yī)療器械注冊(cè)證/備案憑證（NMPA） 醫(yī)療器械生產(chǎn)許可證 進(jìn)出口經(jīng)營(yíng)權(quán) 目標(biāo)市場(chǎng)準(zhǔn)入認(rèn)證： 歐盟CE認(rèn)證（注意2025...
How to become a total export agent for pharmaceuticals? These six key issues must be clarified.
August 1, 2025
如何選擇醫(yī)藥出口總代理機(jī)構(gòu)？ 選擇醫(yī)藥出口總代理需重點(diǎn)考察三個(gè)維度：專(zhuān)業(yè)資質(zhì)、行業(yè)經(jīng)驗(yàn)和全球網(wǎng)絡(luò)。優(yōu)質(zhì)代理機(jī)構(gòu)應(yīng)具備： 藥品經(jīng)營(yíng)許可證和GSP認(rèn)證 至少5年醫(yī)藥產(chǎn)品出口實(shí)操案例 在目標(biāo)市場(chǎng)擁有自營(yíng)清關(guān)團(tuán)隊(duì) 熟悉WHO預(yù)認(rèn)證及PIC/S規(guī)范 ...
How to do export food trade agency? These 8 key questions must be clarified!
August 1, 2025
如何選擇可靠的食品出口代理公司？ 選擇代理公司時(shí)需重點(diǎn)關(guān)注： 行業(yè)認(rèn)證：需具備ISO22000食品安全管理體系認(rèn)證、HACCP認(rèn)證 操作經(jīng)驗(yàn)：查看近3年同類(lèi)食品出口案例（如冷凍海鮮、乳制品等） 合規(guī)能力：熟悉中國(guó)海關(guān)總署第248號(hào)令《進(jìn)出口食品安全...
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