Personnel Management

R&D Team: Our employees are highly educated in medicine, pharmacy, and chemistry, over 35% of whom have a master’s or doctoral degree. With mastery of research skills, they are qualified to fulfill their R&D responsibilities.

Personnel Training: Regular training sessions - on professional skills, quality system knowledge, project management, external equipment, and industrial laws & regulations - enable our people to learn, understand, and grasp latest laws, regulations, institutions, and technologies.

Our organizational structure is tailored for medicine R&D by including an independent quality management department and supportive divisions.

Facility Management

We establish experimental facilities suited to research needs and keep control and record of the R&D environment. The facilities are well deployed and in sound operation.

Our company is equipped with instruments and facilities for research and experimentation, which are well placed and clearly specified with complete qualifications. Specialized personnel are responsible for management of instruments and facilities by regular examination, cleaning, maintenance, testing, verification, calibration, and record-keeping. Also, they are continuously upgraded for research needs and requirements of laws and regulations.

Material Supply Management

With a sound system for material management, specialized personnel are responsible for management of raw and auxiliary materials, reagents, reference materials, reference preparations and other materials. The source is controlled through supplier audit. At receiving materials, they collect and sort source certifications. The materials are kept according to storage conditions and marked with clear specifications. The use records of the materials are well managed.

Documentation Management

We have established a sound management system of documentations and files that conduct systematic design, formulation, review, approval and distribution of documents and their unified classification and numbering. With the quality management system, effectiveness of original records and sustainability of R&D progress are monitored to ensure scientific, standardized and integral drug R&D conduct. Major management procedures – including documents, personnel, equipment, materials, laboratories, computerized systems, data, and system audit – are continuously improved and upgraded to meet the requirements of relevant laws and regulations.

Logistics Management

Expert guidance and full participation are giving a constant boost to quality awareness of the leadership and researchers;

We strike a balance of compliance and operability as well as of regulation and efficiency;

The quality management department performs supervision and execution to realize stepwise improvement by regular self-evaluation and optimization.