Our location in Indonesia gives us a favorable condition for the implementation of clinical research:

• Indonesia has population more that 200 million with 300 ethnics origin
  
• Variety of disesase prevalence
  
• Numerous study sites and investigators
  
• Competitive trial cost
  
• ICH-GCP guideline has adhered by National Drug Regulatory Authority, Ethics Committee, and all clinical research professional
  
• Experienced clinical laboratory which has international standard facilities spread out through the country
  
• Availability local and global experienced CRO

In serving clinical trial, our effective and efficient project management handled by professional and GCP certified personnel will ensure high quality process, cost-effective project, good monitoring system and implementation, reliable study result, timely study completion, and post-study services, that comply with international standards and regulatory authority requirements.