CLINICAL SERVICES

Clinical Research Consultants provide expert planning, management, and preparation of study materials. Experienced in clinical trial design, study management, monitoring, and statistical analysis for both pre-market and post-market studies, we supplement our expertise by working alongside expert medical and statistical consultants whenever the need arises. We work hard to be both effecient and cost-effective for our clients.

CRC's full range of clinical services include:

Preparing Study Materials

• Clinical protocols
• Case Report Forms
• IRB submission materials and informed consent documents
• Study handbooks and Investigator Agreements.

Managing and Monitoring Trials

• Identify and evaluate potential sites/investigators
• Provide liaison with IRBs and FDA
• Conduct investigators meetings/train site personnel
• Monitor/audit sites to verify protocol compliance

Providing Data Management and Statistical Analysis

• Database and data entry screen design
• Data Quality Control, coding, entry, and verification
• Statistical analyses and clinical report preparation

CLINICAL | QUALITY & COMPLIANCE | REGULATORY