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Site Management

Site Management

Our highly experienced and motivated team of CRAs provide all site management services which ensure that your clinical trial operates within the requirements of ICH GCP, and is run efficiently and meets all critical timelines during the study conduct These services include:

  • Site staff training
  • GCP and protocol compliance
  • Patient recruitment strategies
  • Essential document review, collection, and processing
  • Source documentation review, CRF review and query resolution
  • Accountability for all study documents and materials
  • Safety Monitoring and reporting
  • Management, review and accountability of Investigational product in conjunction with pharmacy staff
Service:  

Clinical Development