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Clinical Monitoring

Clinical Monitoring

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We aim to employ and retain top-notch CRAs with at least 2 years of experience in monitoring. We always ensure that our monitors are highly educated, properly trained and have demonstrated site monitoring proficiency before being allocated to a study.

As clinical research is rather new to the Middle East region, we always ensure to assign local CRAs to monitor sites in their home countries, providing understanding of local regulations, customs and business practices.

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Study Feasibility

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Medical Writing

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Regulatory Support

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Clinical Monitoring

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Project Management

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Biostatistics Services

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Patient’s Recruitment & Retention Programs

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Health Economics

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Support to Study Site Staff

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Insourcing & Outsourcing

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Electronic Solutions (eCRF, digital tablet)

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Trainings & Workshops

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Data Management

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Staffing Services

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Patient Support‍ ‌Programs