Clinical Trial Site Management
Site Feasibility and Investigator Selection
Clinical Monitoring
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 offers a growing network of site monitoring services. Monitors are selected for their professional experience and interpersonal abilities, essential for effective interaction with site personnel, and adhere to stringent NOMAD Life Sciences monitoring SOPs. They are skilled in the review of data and source document verification on site, and use standardized templates for all queries and reports.

Our monitoring team has thorough knowledge in ICH GCP guidelines and local and international regulatory guidelines.

Our monitoring services include:
  1. Investigator Identification
  2. Site Qualification Visits
  3. Key Personal Trainer
  4. Planning Investigator Meetings
  5. Site Initiation Visits
  6. Site Staff GCP and Protocol Training
  7. Interim Monitoring Visits
  8. Blinded and unblended IP Accountability
  9. Close Out - Study Termination Visits