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Clinical Trial Management

As a worldwide single-source provider for clinical trial planning, trial management and drug development planning, BIOTECH Consultancy Services is helping biotechnology and pharmaceutical companies by delivering the best total solution - and all the support required – to optimize the return on your clinical research investments. And we accomplish that in the quickest, most responsive and economical way possible.

Our approach is driven by a critical mass of clinical research expertise, the ability to identify and focus on the most significant challenges, and your need for prompt results. Our world-class insight and experience in the most significant challenges, and your need for prompt results. Our world-class insight and experience in the development and execution of clinical research plans and protocols delivers the decision support you need to chart your next clinical move.

Project Management
  • All stakeholders’ relationships and communication
  • Project resource planning, allocation, scheduling and analysis
  • Manage grants and budgets
  • World grants and budgets
  • World class proprietary CTMS application to manage projects and process
Projective Services
  • PSSV: Pre-study Site Selection Visits
  • Investigator networking
  • Quicker patient recruitment with our unique access to healthcare organizations
Clinical Trial Process
  • Preparation of protocols and CRF Design
  • Clinical trial site qualification and initiation
  • IFC/IRB approval
  • Investigator and patient recruitment
  • Clinical trail and supplies management (IMP Shipment)
  • Supporting laboratory and pharmacy services
Clinical Trail Monitoring and Tracking
  • Pre-study & initiation visits
  • Monitoring visits
  • Source document verification
  • Close our visits
  • Trial document handling
Medical/Safety Monitoring
  • Patient safety monitoring
  • Adverse Event reporting
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