Clinical Trial Services
Next to acting as the Maastricht UMC+ trial office, CTCM also functions as an independent academic Contract Research Organization (CRO) with extensive experience in conducting all types of industry-sponsored and investigator-initiated research, ranging from national single-center to European multi-center clinical studies. We offer various customized services throughout the entire research process, if necessary in collaboration with qualified vendors, to make your clinical study a success. For example, we collaborate with partners in the areas of methodology and statistics, pharmacovigilance, and data reuse (data requests).
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CTCM offers consultancy and broad data management support that best suits your needs.
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Before the start and during your clinical study, CTCM can provide support with the submission, necessary approvals, amendments and notifications.
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CTCM offers an extensive monitoring service for the quality assurance of research which is subject to the WMO.
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CTCM has extensive experience in organizing, coordinating and supporting clinical research and can take care of the complete coordination of your study, or part of it.