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TCA Clinical Research Ltd. provides a full range of services to support, facilitate and manage Phase I, II, III & IV studies, feasibility studies and non-interventional studies. Our top quality services have been fine-tuned to ensure work in a timely, cost effective manner, and include:
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• Pre–study support
• Completion of regulatory and ethics
submissions
• Local site evaluation, selection and
management
• Patient recruitment support
• Monitoring from study initiation through
closure
• ICH-GCP training of investigator site
personnel
• AE management
• Communication with the sponsor and
regulatory authorities (including audits &
inspections)
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• Contracts negotiation with sites and
budget control
• Coordination of study closure and
query resolution
• Project Management
• QA Management
All of our services are in accordance with ICH-GCP guidelines, sponsor’s SOPs (and/or our own SOPs), FDA regulations and Israeli Health Authorities' regulatory guidelines.
We are committed to meet or exceed our clients' expectations, therefore maintain professionalism, efficiency, reliability, precision and above all - excellence in everything we do.
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