Clinical Trial Site Management
Site Feasibility and Investigator Selection
Clinical Monitoring
NOMAD Life sciences conducts the site feasibility's to identify potential sites for a particular therapeutic area and also identifies the suitable investigators for a particular indication. We identify investigators & sites for CRO's and pharma company's depending upon the therapeutic area The Site identification & investigator selection is done based on following points
  1. Patient load
  2. Investigator's qualification and interest
  3. Hospital infrastructure and resources
  4. ICH/GCP trained staff availability
  5. Papers published by the Investigator
  6. Investigator's and site's previous experience on clinical trial
  7. Complete site feasibility with infrastructure and as per protocol-specific requirements and specifications
Audits
Medical Writing
Quality Assurance and Auditing ensures that the trials are conducted and data are generated, documented and reported in compliance with the protocol, GCP and other applicable regulatory requirements. NOMAD Life Sciences Quality Assurance and Audit Solutions team is experienced in providing exceptional and timely service GCP, GLP Audit and Quality Assurance solutions customized to meet your project-specific needs.

NOMAD Life Sciences operations team has managed investigative site that has undergone successful EMEA GCP Audit.

We also conduct following audits as per the requirement.
GCP Audits
In House Audits
Site Routine, For Cause Audits
Document Audits
Pharmacovigilance
Other Services
  1. Clinical research consultancy
  2. Clinical Research Site set up
  3. ICH - GCP Training
  4. SOP preparation
  5. Constitution of Ethics Committee

Nomad Life Sciences provides trained clinical research coordinators to the sites to conduct the clinical trials.
  • Pre trial:
  1. Identify Sites, potential Investigators
  2. Site set up
  3. Document collection
  4. Prepare site for SIV
  • During the trial:
  1. Assist in the informed consent process, screening ,randomization
  2. Coordinate subject study visits (Scheduled / unscheduled)
  3. Manage Clinical trial material accountability , distribution & logistics
  4. Coordinate with local & central lab logistics as per the study requirement
  5. Preparation, attendance and follow-up of monitoring and audit
  6. Subject reimbursements
  7. Maintain and update trial master files
  8. Coordinate SAE reporting on time
  9. On time completion of Case report form
  10. On time study related query resolution
  • Post-trial:
  1. Coordinate Close out visit
  2. Archival at site