Foundation Clinical Research (FCR) provides clinical trial study start-up expertise and assistance to the pharmaceutical, biotechnology and Contract Research Organization (CRO) industries.

FCR focuses its expertise exclusively on the clinical trial study start-up process and has a reputation of excellence among the world's leading pharmaceutical, biotechnology and CRO organizations. Superior flexibility coupled with our industry extensive knowledge is what has made us the preferred choice as an outsourcing partner. Our commitment to customer service allows us to fulfill all your clinical trial needs.

FCR recognizes the study start-up component of a clinical trial is vital to its success. We focus our energies on meeting your study start-up needs to ensure your sites are ready for enrollment promptly. Our top priority is to provide you with on time, high quality and cost effective results. We are there for you from start to finish!

Site Identification

Execution of Confidentiality Disclosure Agreements (CDAs)

Pre-study/Qualification Visits

Collection of Core Regulatory and Financial Documents

Preparation/Distribution of Initiation Packets and completion of Site Initiation Visits

Site Training

Review and Approval of site specific Informed Consent Forms (ICFs) and assistance to clinical sites with central and local institutional review board (IRB) submissions and approvals

Contract and per patient budget negotiations

Contact Information

Foundation Clinical Research, LLC
Richard C. Arslan, President
2776 S. Arlington Mill Dr., Suite 517
Arlington, VA 22206 USA
Phone: 703-820-1204
Fax: 703-820-1205
E-mail:

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