Clinical Trials Management

Our experienced Clinical Project Managers are responsive and proactive, and ensure that the right resources are used with established procedures to maximize efficiency throughout your study.

Most of all, we honor our commitments, and take ownership of our work, and aim to be a partner with whom you face and overcome challenges in clinical development by leveraging increasingly limited

Key activities

  • Status Reporting to Sponsor and CRO

  • Contacts (update) with Investigators/Ethical Committees

  • Meeting CRO – Sponsor

  • Meeting with Steering Committee

  •  Ongoing archiving of TMF, TCF and other Clinical Trial documents

  • Long Term Archiving of Clinical Trial documents

  • Development of Clinical Trial specific Procedures & Reports

  • Regulatory Assistance

  • Legal Assistance

  • CRO Personnel On-site