FSP Onsite Monitoring

Onsite and Central Monitoring

At PPD, remote site monitoring is nothing new

Our skilled and well-trained clinical research associates (CRAs) ensure the highest quality review of data and effective interaction with study sites.

When on-site monitoring visits are not an option, our highly-capable CRAs:

  • Oversee data collection
  • Review source documentation and case report forms
  • Ensure regulatory compliance
  • Resolve data queries
  • Conduct interim analyses as requested by clients

As the industry continues to evolve, virtual monitoring will become a must, not a maybe. We have the expertise and experience to get your remote site monitoring underway and make your transition to clinical trials of the future a smooth one.

Our experienced CRAs are well-trained and highly qualified to conduct remote monitoring and:

  • Demonstrate site monitoring proficiency to PPD management before being assigned to a study
  • Typically dedicate to one protocol at a time to maintain quality
  • Are assigned to monitor sites in their home countries (in Europe and Asia), providing understanding of local languages, regulations, standards of care, customs and business practices

Interested to learn more?