Culture & Values
Subsidiaries & Joint Ventures
Diversity & Inclusion
Sustainability & ESG Report
Safety & Toxicology
Data Management and Statistical Analysis
Clinical Development Strategy
Site Management (SMO)
Medical Device / IVD
Multi-region Clinical Trial (MRCT)
Vaccine Clinical Trial
Functional Service Provider (FSP)
Multi-Regional Clinical Trials (MRCT)
Ready to start your global clinical trial project with full speed and excellence.
Global Enabling Platform
Drug development has been globalized, and Multi-Regional Clinical Trials (MRCT) for regulatory submission has widely been conducted by global biopharmaceutical companies with the objective of reducing the time lag of launch in key markets and improve patient access to new and innovative treatments.
Tigermed offers cross-nation and cross-function full CRO services for global clinical trials. We are supporting our partners' MRCT projects in 41 countries and regions in oncology, vaccine, cardiovascular disease, etc. Our MRCT efforts improve transparency and safety for clinical trial research participants around the world by creating and implementing ethical, practical and regulatory solutions.
We Are Supporting Our Partners’ MRCT Projects in 50 Countries and Regions
We Are Supporting Our Partners’ MRCT Projects in 30 Countries and Regions
Hong Kong China
Global Project Management (GPM)
Central point of contact between sponsor, sites, medical and technical team, clinical monitors and quality control unit, etc.
GPM team with global presence in 4 continents with world-class project management experience
Local know how and professional expertise in local regulatory policy
Provide customized Regulatory + Clinical solutions highly matched with local study
Seamless communication even with cultural differences
Local Clinical Operation Team
CPM and CRA across 50+ countries to support your global trials
Global SOPs and budget protocol, localized contracting process, country level site contract template
Strategic CRO partners in 30+ countries in Africa, Middle-East and APAC
Integrated Solutions and Services
Regulatory experts dealing with NMPA, FDA, EMA, expertise in global regulatory pathway and clinical development protocol
Centralized service hub in China including MW, MM, CTA, DMBS, PV, Central Lab, Central Imaging, etc.
Consolidated Tigermed global SOPs complying with ICH-GCP, local GCP and all other applicable regulations