About Noahpharm
Beijing Noahpharm Co., Ltd. is a wholly-funded subsidiary of the publicly traded company Beijing Sun-Novo Pharmaceutical Research Co., Ltd. (stock code: 688621). With a registered capital of RMB 10 million, Beijing Noahpharm Co., Ltd. is a CRO to provide the professional clinical trial solution for pharmaceutical and medical device manufacturers. The company owns a powerful clinical medical & registration team, superior clinical site resources, a well-established quality assurance system, and an experienced clinical monitoring and project operation team. The company provides all-round technical services for pharmaceutical and...
Company founded
Over 400 Cases
Registered Capital
Over 200 Staff
Innovation Service
One-stop solution, securing human health and welfare
Noahpharm owns a group of high-quality clinical experts and a well-trained medical team, and enjoys a good reputation for acquiring the high-quality clinical trial data and meeting customers’ expectations on clinical development
Noahpharm provides customers with all-round clinical operation services covering from the early clinical trial to final approval for marketing of the drug. We are not only responsible for the sponsor, but also assume the same commitment
Data Management & Statistical Analysis
Noahpharm provides customers with all-round clinical operation services covering from the early clinical trial to final approval for marketing of the drug. We are not only responsible for the sponsor, but also assume the same commitment
Noahpharm’s quality management system focuses on control of study specific risks, and ensures data integrity and subject protection and safety. In accordance with the quality management principles, GCP guidelines and pharmaceutical regulatory requirements, we follow the company policy and project control requirements
Noahpharm can provide professional registration services for chemical drugs, biological products and medical devices, assist drug development and shorten the time to market. During product registration, the rich practical experiences enable Noahpharm to precisely grasp product registration essentials.
To become an international CRO with leading service quality
securing human health and welfare”, adheres to the idea of “pursuing quality and scientific innovation”, observes the principle of “win-win and virtue
News Center
Insight & R&D news
In order to speed up the establishment of an evidence system for the registration and evaluation of Chinese medicine which combines the traditional Chinese medicine (TCM) theory, human experience and clinical trial, standardize the writing of application documents for TCM theory and package inserts for TCM compound preparations of classic famous formula, under NMPA deployment, the Center for Drug Evaluation has coordinated formulation of the Guideline for Writing of Application Documents for Traditional Chinese Medicine (TCM) Theory of New TCM Compound Preparations (Trial) (Attachment 1), and the Guideline for Writing of Package Inserts for TCM Compound Preparations of Classic Famous Formula (Trial) (Attachment 2). In accordance with the Notice of Comprehensive Division, NMPA on Releasing the Technical Guideline for Pharmaceutical Products (YJZYG [2020] 9), after NMPA review and approval, it's hereby released and implemented since the date of release.
Noahpharm Presence in SAPA2021 China
Noahpharm Presence in SAPA2021 China
On October 14-15, 2021, hosted by Sino-American Pharmaceutical Professionals Association – China (SAPA-China), and guided and organized by the Management Committee of Suzhou High-tech Zone and the Management Committee of Suzhou Hushuguan Economy and Technology Development Zone, the Opportunity and Challenge for Chinese Biological Medicine Development and SAPA2021 China kicked off in Shishan International Convention Center in Suzhou High-tech Zone.
In golden autumn, Beijing Noahpharm Co. Ltd moved to a new address on October 11, 2021.The new office is situated in 3rd Floor, Building 11, Zone 4, Hanwei International Plaza, Fengtai Science and Technology Park, Beijing. The superior geological location and convenient transportation shorten our communication distance with customers, helping us meet customers’ demand in a better and faster way. The new location also facilitates employee mobility.
Provisions for the Supervision and Administration of Drug Production (No. 28 Order of the State Administration of Market Regulation, January 22, 2020)