gogogo日本免费观看,18禁成人网站免费观看,亚洲日韩精品欧美一区二区,中国青年gary东北大飞机打桩

Stock(600222)Hot line:010-83057670

MAH

Leader of "0" Cost MAH 3.0 Era

CDMO

Macromolecule Drug CDMO Platform

1.Platform Overview
 

Macromolecular platforms comply with GMP Standards of US FDA、EU EMA and NMPA of China. It equipped with 500L/2000L scale production line (designed by NEPHARM, with cGMP standards, equipped with Sartorius Bioreactor, Millipore System and GE Purification System, Bosch washing & drying & irrigation & rolling linkage line, 3M sterilization cabinet and Schneider SCADA Automation Control System).

The core personnel of the platform operation team have more than 15 years  work-experience in Internationale-leading pharmaceutical and biotechnology companies such as KANGHONG, INNOVENT and Bristol-Myers Squibb, and have rich experience in process development and scale-up, process control and quality control, project management, etc., and have experience in the marketing and R&D and production of 8 biological drugs.
 

2.Service Content

The platform can provide stable cell line screening, pilot fermentation process, large-scale culture process and macromolecular purification process development services, antibody drugs, recombinant protein drugs, protein vaccine pilot and large-scale production services and other biological macromolecular pharmaceutical preparations production technical services, support products in China, United States, Europe and other places to conduct clinical trials and rapid marketing, and achieve global synchronous transformation of customer research results.


3.Reality view
 

 

 

Small Molecule Drug CDMO Platform
 

1.Platform Overview

Zhengzhou Pioneerpharm Pharmaceutical Co., Ltd. (Small Molecule API & Preparation CDMO Platform) is an organic part of the Lifezhengzhou · Leadingpharm CXO System. It is jointly built by Leadingpharm, Beijing Chempion Biology and Lifezhengzhou Biomedical Park, provideing technical services related to small molecule industrialization and clinical sample preparation for national pharmaceutical enterprises.
The platform complies with GMP standards of FDA and NMPA, with a total construction area of 6651.54㎡. It is equipped with three preparation workshops (oral solid preparation workshop, small volume injection workshop and oral solution workshop), with supporting power center, storage, quality inspection and other institutions or facilities.

2.Service Content

The platform provides a qualified site for the production of clinical samples of innovative drugs, commercial production of rare disease drugs, pilot test and commercial production of imitation drugs. The dosage forms include tablets, capsules, granules, oral liquid, small volume injection and other conventional oral and injection dosage forms.
The platform can produce 200 million preparation units of solid preparations, 15 million preparation units of injections, 12 million preparation units of oral liquid, 60 pilot projects and 1000 batches of testing per year, enabling innovative enterprises to break through bottlenecks and grow at a high speed.

3.Reality view

 




 

 

 

 

 

大名县| 塔河县| 娄烦县| 澄城县| 黑山县| 三江| 孝感市| 安庆市| 永昌县| 新昌县| 积石山| 深州市| 庆云县| 文化| 广平县| 贵南县| 黄陵县| 芮城县| 林甸县| 偏关县| 永济市| 高密市| 黄石市| 留坝县| 汕尾市| 克东县| 姜堰市| 浙江省| 滦南县| 仁怀市| 闽清县| 工布江达县| 迭部县| 双流县| 阿拉善盟| 博客| 龙岩市| 马关县| 南靖县| 双流县| 鄂温|