Clinical Research

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Andronovo Labs acts as a common platform between the Principal Investigator(s) and study Sponsor(s)/CRO(s) for the successful execution of clinical trials. Having an operating base at Hyderabad

Andronovo Labs deals in Clinical Site management for both Sponsors and Investigators. We have 25 clinical research sites & large no. of satellite sites in PAN India Basis. Andronovo Labs activities for Clinical Site management are

  • Site feasibility
  • Site Selection
  • Trained Clinical Research Coordinator Support
  • Multiple Therapeutic Area
  • Clinical trial training for Investigator & Site Staff
  • Site Qualification & Selection
  • Managing the site
  • Regular Internal Audit by certified Lead Auditors • Completion of CDA
  • Undertaking by the Investigator
  • Form FDA 1572, Clinical Trial Agreement (CTA) etc.
  • EC Submission
  • Meeting the quality to protocol compliance
  • Patient follow-up, safety reporting, IP accountability
  • CRF completion (paper/e-CRF) and compliance with ICH-GCP and applicable regulatory guidelines

Our Expertise

  • Network of good Hospitals /Investigators/ Study Coordinators
  • Certified Lead Auditors for Internal Audit
  • Regular MRM (management review meeting)
  • Satellite Site Networking
  • Rescue Recruitment

Patient Recruitment Services

Recruiting qualified and compliant patients within a study enrollment window is the most challenging aspect of any clinical research.

Andronovo Labs also provides patient recruitment services. Andronovo Labs works with clients and study sites to identify barriers to on-time enrollment and develops a Patient Recruitment Plan for the study. We remain in constant contact with each site to assess the screening process and are always available to support sites and respond to questions regarding patient eligibility and study questions in general.

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