Clinical Studies

PK/PD and Patient Studies

We offer best-in-class services in identifying CRO, negotiate the budget to conduct Patient population PK studies and clinical endpoint studies on healthy volunteers and patient population to assist you with your drug development programs. 

Trial Management

Our Project Managers work effectively and diligently to manage critical aspects of the study and ensure on-time delivery of results, within budget and with the high quality

Creation, collection and review of regulatory documentation

  • Correspondence with IRB/IEC and concerned authorities
  • Trial and site management
  • Management of budget and project timelines

Trial Monitoring

Our skilled and well-trained clinical research associates (CRAs) ensure the quality of data and maintains effective communication with study site coordination’s. Our CRAs conduct on-site visits on periodic basis during the study to

  • Oversee data collection
  • Review source data and case report forms
  • Ensure regulatory and protocol compliance
  • Resolve data queries