Clinical Research Consultants provide expert planning, management, and preparation of clinical studies. The team is 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 efficient 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 investigator 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
