The "Specifications for the Supply and Management of Drugs Used in Clinical Trials of Biological Products," jointly issued by the China Vaccine Industry Association and the China Standardization Association, was developed and drafted with the participation of Huaren Pharmaceutical Clinvantage. It is a normative standard document in China for the supply and management of drugs used in clinical trials of biological products.
2025/08/08
The "Specifications for the Supply and Management of Drugs Used in Clinical Trials of Biological Products," jointly issued by the China Vaccine Industry Association and the China Standardization Association, was developed and drafted with the participation of Huaren Pharmaceutical Clinvantage. It is a normative standard document in China for the supply and management of drugs used in clinical trials of biological products.
2025/07/16
The "Specifications for the Supply and Management of Drugs Used in Clinical Trials of Biological Products," jointly issued by the China Vaccine Industry Association and the China Standardization Association, was developed and drafted with the participation of Huaren Pharmaceutical Clinvantage. It is a normative standard document in China for the supply and management of drugs used in clinical trials of biological products.
2025/06/18
The "Specifications for the Supply and Management of Drugs Used in Clinical Trials of Biological Products," jointly issued by the China Vaccine Industry Association and the China Standardization Association, was developed and drafted with the participation of Huaren Pharmaceutical Clinvantage. It is a normative standard document in China for the supply and management of drugs used in clinical trials of biological products.
2025/06/11
The "Specifications for the Supply and Management of Drugs Used in Clinical Trials of Biological Products," jointly issued by the China Vaccine Industry Association and the China Standardization Association, was developed and drafted with the participation of Huaren Pharmaceutical Clinvantage. It is a normative standard document in China for the supply and management of drugs used in clinical trials of biological products.
2025/06/04
Clinvantage International Clinical Supply Management Center Opens
On June 26, 2024, the "International Clinical Supply Management Center" of Clinvantage (Beijing) Pharmaceutical Technology Co., Ltd. (referred to as "Clinvantage"), a subsidiary of Guanghang Seng Group, opened in Shunyi District, Beijing.
2024/06/28
Shelf validity guidelines and some standards
Shelf validity refers to the period during which the goods maintain their quality, performance and safe use on the shelf.
2024/10/10
Must see! Twelve Evaluation Requirements for Packaging Materials of Sterile Medical Devices
Sterile medical devices are an indispensable part of modern medical field, and the selection and evaluation of their packaging materials are very important.
2024/10/10