Your study deserves a partner who delivers timely, efficient, and high-quality execution - ensuring your clinical trial progresses smoothly and meets its goals.
Myrtle Clinical
Beyond CRO.- Independent Global Clinical Trial Solutions
Israel / Europe / Americas / Asia-Pacific / Middle East
Myrtle Clinical provides flexible CRO services tailored to the specific needs and budget of each study. This adaptable model enables me to deliver excellence and ensure on-time project completion.
By assembling expert local teams across multiple regions, Myrtle Clinical provides expert clinical trial execution through a flexible CRO model, with experienced professionals based in the U.S., Europe, Latin America, Asia-Pacific, the Middle East, and beyond.
We Specializing in the management of complex multi-center, multi-continental clinical trials. Builds and leads tailored local teams, including CRAs, data managers, statisticians, regulatory specialists and more, to ensuring expert coverage in each region. We oversees site selection, operational management, vendor coordination, regulatory submissions, and compliance with international and local standards.
Manages budgets, payments, and contracts . Acts as the central liaison among sponsors, sites, vendors, and regulatory authorities to ensure seamless communication and timely study completion.
Contact us : hadasn@myrtleclinical.com
This comprehensive approach ensures operational excellence and successful trial outcomes.
Accelerating Clinical Trials
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Tailored solutions to speed up patient recruitment and reduce timelines.
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Efficient project management to minimize delays and optimize trial progression.
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Strategic planning and execution to ensure rapid and high-quality results.
Ensuring Compliance with Complex Regulations
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Regulatory submissions to Ethics Committees (IRB/EC) and Health Authorities worldwide.
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Strict oversight of trial activities to ensure compliance with ICH-GCP and local regulatory requirements.
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Comprehensive monitoring of clinical trial data to ensure accuracy, completeness, and protocol compliance.
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Preparation and support for regulatory inspections, audits, and quality assurance processes.
Managing Multi-Center Clinical Projects
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Proven expertise in coordinating and managing multi-center clinical studies.
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Seamless communication and synchronization between teams, sites, and vendors.
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Full transparency throughout all phases to ensure timely and successful outcomes.