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We recognize that each customer’s needs are unique, and we strive to provide innovative, responsible and effective solutions. Our staff works with our clients to prepare, conduct and complete their clinical research—ensuring compliance with FDA and other regulations. Our support has ranged from designing the clinical plan and preparing the Investigational New Drug (IND) applications to conducting Phase I – III trials under Good clinical Practice (GCP) guidelines and submitting the final clinical study report.
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CRM supports product development with a range of services including Clinical Research Services, Clinical Data Management Systems, Statistical Support, and Regulatory Operations. For a complete list of services containing detailed descriptions of CRM’s capabilities and expertise, click here. |
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CRM views collaborative support as a “Win – Win” opportunity. We have assisted research scientists with proposals to win new funding, arranged for collaborative agreements between industry and government laboratories and have developed marketing communications for groups required to attract outside business. Click here to learn more about successful projects utilizing CRM’s collaborative support. |
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CRM will enhance your on-site location with our expertise by providing excellent staff managed by CRM specialist in the field. CRM is recognized for managing programs with low attrition rates and productive employees… Why? |
CRM can support both commercial and government clients. CRM has contract agreements in place with several government agencies.
To request more information concerning CRM’s contract services, collaborative support, management support and/or on-site staffing, contact CRM’s business development office at 301-620-1987 or busdev@clinicalrm.com.
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