Contact us : hadasn@myrtleclinical.com
This comprehensive approach ensures operational excellence and successful trial outcomes.
Accelerating Clinical Trials
-
Tailored solutions to speed up patient recruitment and reduce timelines.
-
Efficient project management to minimize delays and optimize trial progression.
-
Strategic planning and execution to ensure rapid and high-quality results.
Ensuring Compliance with Complex Regulations
-
Regulatory submissions to Ethics Committees (IRB/EC) and Health Authorities worldwide.
-
Strict oversight of trial activities to ensure compliance with ICH-GCP and local regulatory requirements.
-
Comprehensive monitoring of clinical trial data to ensure accuracy, completeness, and protocol compliance.
-
Preparation and support for regulatory inspections, audits, and quality assurance processes.
Managing Multi-Center Clinical Projects
-
Proven expertise in coordinating and managing multi-center clinical studies.
-
Seamless communication and synchronization between teams, sites, and vendors.
-
Full transparency throughout all phases to ensure timely and successful outcomes.