Regulatory

Clinical

Biostatistics

Business

Quality assurance

Consulting & training

New Drug, healthcare product and medical device registration in SFDA

BA/BE study

Protocol development

Business development

Problem solving

Regular training

Document preparation

First-in-man

CRF development

licensing

Clinical auditing

Preclinical study coordination

PK/PD study

Data management

Partner & investment hunting

GXP auditing

Project training

Document translation

Clinical study Phase I-III

Sample size calculation

SOP generation and review

R&D Consulting

Phase IV

Randomization and blinding

Patent consulting and application

Pharmaco-economic

SAP generation

Registration consulting

Pharmaco-epidemiology

Integrated statistical and clinical report

Marketing survey and consulting

Marketing study