Clinical Monitoring

Management. Oversight.

The success of your clinical trial depends in no small measure on the quality of the sites and investigators selected to conduct it. PharmaNet/i3 Strategic Resourcing clinical monitoring staff identifies the best sites for your study and provides the management and support necessary for these sites to excel. Upon selection to participate in your study, sites work with a dedicated clinical trial manager who provides organization, support, and guidance for each site throughout the course of the study.

With decades of experience in global trials, we’ve built a substantial database of quality sites with access to patients in a variety of therapeutic areas. We are also continually updating our list through industry outreach and comprehensive advertising/marketing tactics.

Clinical monitoring services include:

  • Study procedures development
  • Source document review
  • Patient eligibility confirmation
  • Patient compliance tracking
  • Supply inventory management
  • Adverse events reporting
  • Regulatory compliance monitoring
  • Regulatory documentation maintenance

Contact us to see
how we can help you