Bestudy service is including clinical trial design, organization, operation and management of phase I-IV local and global multicenter studies for innovative drug and medical device. These include but not limit to project design and preparation, IND/NDA, protocol medical writing, site selection and collaboration, clinical and medical monitoring, project management and quality control, clinical study self-inspection/CFDA，FDA inspection support/3rd party audit，drug management，data management and statistical analysis, clinical study report writing, etc. Bestudy also provides pharmacovigilance and post-market drug surveillance service during clinical study and after new product launch. In addition, Bestudy provides regulatory consultancy, agent service, HEOR for innovative new drug and medical device planned for China market launch, market launch, market entry. We also provide professional training for improvement of technical skills and talents for investigator and professionals in clinical and pharmaceutical medicine industry.