Full service in clinical trials

Our core skills are centered on clinical data collection and data management. At the heart of these activities is OnlineCRF. Everything we perform in the sphere of clinical data management is professional and effective. Our core activities start from the approved CRF / study protocol and spread to the database lock.

However, what if a client requires a broader spectrum of services? What is our approach when we begin communication at a stage where CRF and protocol have not been created yet?

In many cases, SAS programming, on-site monitoring, regulatory services, logistics, statistical analysis, insurance, and other services are required. Some of these areas are covered by utilizing the resources of Pharmaxi’s regulatory or clinical operations departments. Additionally, we involve our trusted providers to include specific activities or distant geographic locations.

Here are some service categories covered by us:

  • Medical Writing and Translation
  • Feasibility and Site Selection
  • Project Management
  • Clinical Site Management
  • Clinical Trial Monitoring
  • Statistical Services
  • Clinical Data Management
  • Pharmacovigilance
  • Quality Management
  • Regulatory Affairs
  • Logistics Management
  • Preclinical Research
  • Clinical Laboratory
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