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NMPA inspection rejection by Daewoong Bio Inc leads to import, sale and use suspension

China’s NMPA has suspended the import, sale and use of Cefodizime Sodium for injection by DAEWOONG BIO Inc following its rejection of an NMPA inspection request at its production site.

August 28, 2024
NMPA inspection rejection by Daewoong Bio Inc leads to import, sale and use suspension
Innovative Medical Device from Shanghai Wicresoft approved by NMPA

China’s NMPA has approved Shanghai Wicresoft’s Bioabsorbable Rapamycin Eluting Coronary Stent System through the Innovative Medical Device Green Pathway Programme.

August 28, 2024
Innovative Medical Device from Shanghai Wicresoft approved by NMPA
NMPA import suspension of SAMO SpA medical devices

China’s NMPA has announced a suspension of import, sale and use of two medical devices manufactured by SAMO S.p.A. because they failed to comply with regulatory requirements.

August 29, 2024
NMPA import suspension of SAMO SpA medical devices
Innovative new drug clinical trial approval pilot program

China’s NMPA has issued a pilot program to optimize innovative new drug clinical trial review and approvals. in Beijing and Shanghai have been approved as the first pilot regions.

August 28, 2024
Innovative new drug clinical trial approval pilot program
China electric bicycle charger and Lithium-ion battery CCC Certification implemented

China electric bicycle charger and Lithium-ion battery CCC rules were released by the National Certification and Accreditation Administration on July 29, 2024.

March 11, 2026
China electric bicycle charger and Lithium-ion battery CCC Certification implemented
MDACS Listing: Key to Hong Kong Public Procurement and GBA Market Entry
MDACS Listing: Key to Hong Kong Public Procurement and GBA Market Entry

MDACS listing is more crucial now for Hong Kong public procurement, especially for MedTech companies looking into entering the GBA market

January 16, 2026
MDACS Listing: Key to Hong Kong Public Procurement and GBA Market Entry
China Clinical Trial Exemption List Update 2024 – Draft for Comments

China’s CMDE has issued a Draft for Comments on its latest update to the Clinical Trial Exemption List. The deadline is August 30, 2024.

August 7, 2024
China Clinical Trial Exemption List Update 2024 – Draft for Comments
GMP for Excipients and GMP Guidelines for Packaging Materials in China

China’s NMPA has issued a draft for comments on an updated Good Manufacturing Practice – GMP for Excipients and Packaging. The deadline to submit feedback is 20 August 2024.

August 28, 2024
GMP for Excipients and GMP Guidelines for Packaging Materials in China
China Medical Device Registration for June 2024 on trend with 2023

China Medical Device Registration for June 2024 were on trend with 2023 overall approvals. Here are some charts to summarize this.

August 6, 2024
China Medical Device Registration for June 2024 on trend with 2023
China Challenge Test Cosmetics Guidelines Released

The NIFDC has released new guidelines for China Challenge Tests Cosmetics for manufacturers selling products to China.

January 27, 2026
China Challenge Test Cosmetics Guidelines Released
Cosmetic Packaging Compatibility Testing Guidelines Released

The NIFDC has released new guidelines for cosmetic packaging compatibility testing. Other guidelines were released together on July 8, 2024.

March 9, 2026
Cosmetic Packaging Compatibility Testing Guidelines Released
Cosmetics Stability Testing

China’s NIFDC has issued new guidelines for Cosmetic Stability Testing for cosmetic manufacturers selling products to China.

August 1, 2024
Cosmetics Stability Testing
Veterinary Disinfectant Test Report Templates published by China's IVDC
Veterinary Disinfectant Test Report Templates published by China's IVDC

China’s Institute for Veterinary Drug Control has released 16 Veterinary Disinfectant Test Report Templates.

August 1, 2024
Veterinary Disinfectant Test Report Templates published by China's IVDC
China Veterinary Anesthetic Drugs and Psychotropic Drugs Regulations issued
China Veterinary Anesthetic Drugs and Psychotropic Drugs Regulations issued

China veterinary anesthetic drugs and psychotropic drugs regulations have been published by the Ministry of Agriculture on July 11, 2024.

August 1, 2024
China Veterinary Anesthetic Drugs and Psychotropic Drugs Regulations issued
China Electric Bicycle Battery Certification CCAP Rules Revised

China Electric Bicycle Battery certification rules CCAP-GZ-464204:2024 have been revised and replace the previous version CCAP-GZ-464204:2023.

China Electric Bicycle Battery Certification CCAP Rules Revised
CCAP certification of vehicle batteries has revised rules and requirements

CCAP certification of vehicle batteries has revised rules and requirements. These were published by the CCAP China on April 30, 2024.

March 11, 2026
CCAP certification of vehicle batteries has revised rules and requirements
China Active Pharmaceutical Ingredient Post-Market Changes Guidance

Post-market changes to Active Pharmaceutical Ingredients in China now have clearer guidance thanks to a recently published Q&A from CDE.

July 26, 2024
China Active Pharmaceutical Ingredient Post-Market Changes Guidance
Radio Frequency Device requirements in China updated by NMPA

China’s NMPA has issued an update to Radio Frequency Device Requirements in China on July 8, 2024 to ensure the safety.

July 23, 2024
Radio Frequency Device requirements in China updated by NMPA
China drug approvals of Clinically Urgent Overseas Drugs – draft for comments

The NMPA is requesting comments on China drug approvals of Clinically Urgent Overseas Drugs. The deadline to submit comments is July 24, 2024.

July 18, 2024
China drug approvals of Clinically Urgent Overseas Drugs – draft for comments
AI use cases in Pharma – explored by the NMPA

China’s NMPA has explored numerous AI use cases in Pharma. The scenarios aim to promote AI research and AI applications in drug regulation.

July 17, 2024
AI use cases in Pharma – explored by the NMPA

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