who we are
Beijing LEVA Pharmaceutical Co. Ltd (hereinafter referred to as LEVA Pharmaceutical) is the first CRO company in China that performs Phase 0 drug clinical trials. Founded in 2014, LEVA Pharmaceutical provides one-stop clinical research services, including phase 0 ~ phase IV clinical trials, registration, data management and statistical analysis, bioequivalence test, and GCP audit. As a professional contract research organization engaged in clinical studies and pharmaceutical medicine statistics, LEVA Pharmaceutical endeavors to help you achieve your goal with customized solutions.
Our service covers more than 10 sectors, including oncology, cardiology, respiratory, gastroenterology, pediatrics, neurology, urology, anti-infection, gynecology, endocrinology, rheumatology, stomatology, otolaryngology, and dermatology.LEVA Pharmaceutical cooperated with Beijing Shijitan Hospital on the Phase 0 trial, making it the first CRO company in China to perform such a trial, which has introduced into China the innovative ideas of research and techniques of CRO industry.Under the guidance of China's "Twelfth Five-Year Plan", LEVA Pharmaceutical joins firm hands with Jinan University to establish China's first CRA program -- the master program of Clinical Laboratory Management, with the aim of cultivation of well-rounded and versatile talents for CRO industry.
Equipped with a powerful technical team and a management team with contemporary management awareness, LEVA Pharmaceutical has rich experiences in performing domestic and foreign clinical research projects, as well as abundant clinical research resources and expert databases of multiple fields. We also set up a complete data management system and a quality assurance system.With the perfecting of integrated service, our business branch becomes more diversified. LEVA Pharmaceutical grows rapidly as an innovative company in CRO industry, winning trust and recognition from experts, scholars and partners in the industry.
We have always upheld the notion of "quality orientation, honest service, sincere cooperation, and mutual development", the entrepreneurial spirit of "trustworthiness, professionalism, success, happiness, and honesty". Set foot in China but with a global horizon. LEVA Pharmaceutical is wedded in providing efficient high-quality services with innovative technologies, and establishing an omnibearing and stereoscopic service platform for clinical studies and pharmaceutical medicine statistics.
To be the most respectable partnership research organization
Dedicated to the operability and timeliness of projects and in pursuit of the philosophy "change for you" to achieve mutual success.
Honesty: transparent and open implementation process with users' benefits and interests as first principle.
Win-win: keeping up with the users' objectives to realize common development through cooperation.
Professionalism: providing users with the optimal solution of protocol, technology and talent support to ensure the goal's fulfillment.
Trustworthiness: Delving into the research field to bring innovative ideas to create better values for users.
Happiness: offering attentive services for each user and achieving common goal in harmonious atmosphere.
The Clinical Research Department has a highly-qualified professional clinical research team, including clinical directors of more than 10 years management experience, project managers with 6-10 years management experience, and CRAs with clinical operation experience of at least 4 to 8 projects. Accuracy, rapidness and innovation are our features.
Medical Registration Team
LEVA Pharmaceutical has strong expert resources. With more than 10 years management experience, the Medical Registration Team is able to design clinical trial protocols in a more accurate manner, to provide feasible registration services for domestic and international registrations of medical products, medical devices, health food and cosmetics.
The Audit Team of LEVA Pharmaceutical consists of famous domestic audit experts with rich experience in clinical research, statists with academic experience in USA, and well-known statistical experts. With a set of QA& QC system in line with international standards, we focus on the system audit of clinical research projects for domestic registration.