• WE FORESEE THE FUTURE OF CLINICAL RESEARCH

Our Core Area

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Our Core Area in Clinical Research

 

Project Management

We manage all phase study projects from various clients. Our services in project management includes
  • Conducting various phases of studies
  • Investigator and site selection; and allocation
  • Organizing Investigator meetings
  • Facilitating the study activities
  • Maintain confidentiality
  • Monitor budgets and other financial procedures
  • Management of clinical trial supplies
  • Monitor the study throughput the process

Site Feasibility

We have the network of qualified sites for clinical trials. Our services in site feasibility includes
  • Patient pool for the study
  • Investigator and site feasibility assessment
  • Monitor the facilities available in the site for the study
  • Assessment of a site for similar studies or other clinical study
  • Availability of qualified site personnel
 

Ethics Committee

We don’t fail to extend our service in ethics committee, as it is an important criteria for clinical study
  • Ethics Committee documents preparation
  • SOP preparation
  • EC Registration and Re-registration
  • EC notification
  • EC meeting
  • Regulatory and approval process
  • NABH Accreditation process for Ethics committee

Clinical Trial Coordination

We provide a trained coordinator for all clinical study. Our services includes
  • Initial documentation process before start up of study
  • Site initiation and training
  • Patient enrollment
  • Patient - follow up
  • CRF - review
  • SAE Data Collection
  • Data administration and Management
  • Study Close-up