Clinical Trial Management
Our approach to clinical trial management is strictly guided by ICH and GCP guidelines. Safety of the subjects and research personnel is our first concern. Our fine-tuned processes supported by state-of-the-art technology allow us to ensure patient safety, ICH/GCP compliance, and proper management of timelines within budget.
Our Clinical Trial Management Services include, but not limited to:
Project Management
Protocol and Study Design
Investigator Selection and Recruitment
Regulatory Document Collection and Submission
Investigator Meetings
Investigator Contract Negotiations
Informed Consent Development
Investigative Site Management
Clinical Monitoring
Vendor Management
Study Archiving