Our comprehensive monitoring plan, extensive SOPs, and experienced Clinical Research Associates (CRAs) ensure compliance with domestic and international regulations and guidance. We focus on assuring patient safety and data integrity at all times. We offer the following Clinical Monitoring services:
• Monitoring Plan Development • Investigative Site Evaluation and Selection • Site Initiation, Monitoring, and Close-Out • Training of Study Personnel • Regulatory Document Review • Source Document Verification • Investigational Product Accountability • Regulatory Compliance of Computer Systems • Experienced Staff in the U.S. and Abroad