Clinical Research

临床研究

泰格医药的临床部门由众多临床专家、生物统计学家和训练有素的监查员团队组成。有完善的质量管理和质量控制系统，确保项目过程符合ICH-GCP和中国GCP的要求，并获得高质量的临床研究数据。

泰格医药丰富的临床项目管理经验，良好的医院合作关系和合理的办事处分布，保证了项目的实施进展，缩短整个临床试验的时间，从而使客户的新产品早日上市。

Embedded with a sound quality management and control system, the Clinical Trial Department of Tigermed is also teamed with a group of medical experts, biostatisticians and well-trained CRAs (clinical research associates). Tigermed conducts clinical researches in strict compliance with ICH-GCP and Chinese GCP, and facilitates our clients to obtain credible and high quality clinical data.

With significant clinical trial management experiences, good partnerships with hospitals and broad geographic coverage of branch offices, Tigermed can streamline your clinical research and help you bring the miracle of your new product to market sooner.

临床试验项目策划管理和实施

Clinical Trial Strategy Planning Management and Implementation

临床实验方案和CRF报告、表知情同意书设计，研究者手册撰写

Protocol Development, CRF Design and Investigator Brochure Writing

研究者选择

Selection of Qualified Investigators

临床试验监查和稽查

Clinical Trial Monitoring & Auditing

试验总结报告的撰写

Final Report Processing

GCP 培训

GCP Training

Tel: +86-21-32503700-845

Fax: +86-21-32503707

E-mail: na.gao@tigermed.net

www.tigermed.net