Site Management & Monitoring

Site Management & Monitoring

The global clinical research market currently requires contracting with 95,000 clinical trial sites and recruiting approximately 1,200,000 patients/volunteers annually. Various decisive activities at the site level and at the sponsor’s organization need a precise site management. Our experienced team has proficiency to monitor and audit the clinical study sites as well as ethics committee operations throughout the India with compliance to sponsor’s SOP, protocol and applicable regulatory authority’s guidelines. At Anash, we are committed to provide the highest quality service to our clients. This includes:

  • • Site training
  • • Site initiation, activation, monitoring & close-out visits
  • • Coordination of site contracts and payments
  • • Enrolment and retention strategies
  • • Safety event reporting to EC and Regulatory Authorities
  • • Maintaining central study files
  • • Pharmacy monitoring