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 exactly are medical export agency fees calculated? 2025 latest pricing guide is here!
May 12, 2025
What Specific Items Are Included in Medical Product Export Agency Fees? Medical export agency fees typically consist of three parts: basic service fees + specialized service fees + third-party fees, specifically including: Basic service fees (fixed charges) Agency service fee: 0.8%-3% of goods value (depending on product risk level), Documentation fee: 500-2000 yuan/batch, Customs filing registration fee: 200...
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
How to Choose a Professional and Reliable Export Inspection Agency?
How can medical plastic products expand into overseas markets through agency companies? These key issues must be understood!
June 27, 2025
醫療塑料出口需要哪些特殊資質認證？ 根據2025年最新國際貿易規范，醫療塑料制品出口需重點關注三類認證： 基礎生產資質：ISO13485醫療器械質量管理體系認證 目標市場準入認證： 美國FDA 510(k)或PMA認證 歐盟CE-MDR認證（2020年升級版仍有...
How to become a medical equipment export agent? A comprehensive analysis of the latest compliance points for 2025.
July 13, 2025
一、醫藥器材出口需要哪些資質認證？ 根據2025年最新國際貿易規范，醫藥器材出口需滿足雙重認證體系： 國內強制資質： 醫療器械注冊證/備案憑證（NMPA） 醫療器械生產許可證 進出口經營權 目標市場準入認證： 歐盟CE認證（注意2025...
How to become a total export agent for pharmaceuticals? These six key issues must be clarified.
August 1, 2025
如何選擇醫藥出口總代理機構？ 選擇醫藥出口總代理需重點考察三個維度：專業資質、行業經驗和全球網絡。優質代理機構應具備： 藥品經營許可證和GSP認證 至少5年醫藥產品出口實操案例 在目標市場擁有自營清關團隊 熟悉WHO預認證及PIC/S規范 ...
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