Medical Consumables and Lab Consumables OEM Manufacturer
Medical Consumables and Lab Consumables OEM Manufacturer

News & Events

15 2022.08
Hillgene Was Awarded the TOP 10 Most Promising CXO Companies of [China Biopharmaceutical Industry in 2022]
On August 4-5, the 6th Biomedical Innovation Cooperation Conference and the 2022 China Biomedical Industry Value List Awards Ceremony were held at the Kempinski Hotel Suzhou Jinji Lake. The conference...
15 2022.08
MAH System Stimulates the Vitality of Innovation - Hillgene Empowers the Cellular Therapy Products with CQDMO Services
On July 22-23, 2022, the first International MAH (Marketing Authorization Holder) Cooperation and Innovation Summit was held in Hangzhou.This conference focused on the MAH system, and centered around ...
15 2022.08
Hillgene Reached a Strategic Cooperation with HighthinkMed in Exploring One-Stop Whole-Process Innovative Service Mode for Cellular Therapy Products
Recently, Jiangsu Specoxin Biopharmaceutical Co., Ltd. (hereinafter referred to as "Specoxin Biopharmaceutical") and Beijing Hekinge Pharmaceutical Technology Co., Ltd. (hereinafter referred...
19 2022.07
Innovative and Breakthrough CGT, Best Opportunity and Perfect Timing at Dongtai Hu Lake: CGT Industrialization Summit and First Anniversary Celebration of Hillgene
Innovation breaks through CGT, and the wind and clouds gather at East Taihu Lake! A year ago, Spectrum Bio and Tong Xieyi hosted the "East Taihu Cell and Gene Therapy Industrialization Developmen...
29 2022.06
Official Operation of Hillgene R&D Center, Boosting the Innovation of the Biopharmaceutical Industry in Wuzhong District
This morning (June 28), the ribbon-cutting ceremony for the official operation of Spectrum Biotechnology R&D Center was held. Gu Hongjian, member of the Party Working Committee and deputy director...
27 2022.06
Hillgene Reached a Strategic Cooperation with T-Maximum in Accelerating the innovation and Breakthrough of Universal Cells
Recently, Jiangsu Puxin Biopharmaceutical Co., Ltd. (hereinafter referred to as "Puxin Biopharmaceutical") and Maoxing Biopharmaceutical Technology Co., Ltd. (hereinafter referred to as &quo...
23 2022.06
CDE: Notification of Public Comment Soliciting on “Technical Guideline for the Clinical Research and Development of New Drug Products for Chronic Lymphocytic Leukemia (Draft for Comments)”
Chronic lymphocytic leukemia (CLL) is a mature B lymphocyte clonal proliferation tumor that mainly occurs in the middle-aged and elderly population. Its overall incidence rate is increasing due to the...
20 2022.06
Hillgene Completed the Pre-A+ Round Funding up to Tens of Millions of Dollars Again Constant Enhancing the Capability of CQDMO Services in the Industry of Cellular Therapy Product
Jiangsu Puxin Biopharmaceutical Co., Ltd. ("Puxin Bio" or "the Company") has continued to attract capital attention within two months after the completion of the Pre-A round of fin...
08 2022.06
Important Report from CDE! The Annual Report on Progress of Clinical Trials for New Drug Registration in China (2021)
In order to fully grasp the progress of clinical trials for new drug registration in China, use information technology to improve drug regulatory capabilities, and timely disclose clinical trial progr...
07 2022.06
CDE issued “Guidelines on Clinical Trial Statistics of Drug Products for Rare Diseases (Interim)”
In order to encourage the development of drugs for rare diseases and guide applicants to improve R&D efficiency from the perspective of clinical research methodology, the Drug Evaluation Center or...
01 2022.06
Center for Drug Evaluation (CDE) Issued the Notification of “Technical Guideline for the Pharmaceutical Study and Evaluation of In-vivo Gene Therapy Products (Interim)” (No. 31, 2022)
In order to standardize and guide the pharmaceutical research and development, production and registration of in vivo gene therapy products, under the deployment of the National Medical Products Admin...
01 2022.06
Center for Drug Evaluation (CDE) Issued the Notification of “Technical Guideline for the Pharmaceutical Study and Evaluation of Ex-vivo Genetic Modification System (Interim)” (No. 29, 2022)
In order to standardize and guide the pharmaceutical research of in vitro gene modification systems, under the deployment of the National Drug Administration, the Drug Evaluation Center organized the ...