Service Areas

Our Services

Clinical Professionals, Inc. was founded by medical professionals with the intention of providing outstanding clinical research services to the pharmaceutical and device industries. We are a full-service CRO managing clinical trials across therapeutic areas. We believe in developing strong working relationships with the sponsor and the sites for a successful project. This approach has added to our success in providing quality research on time.

Service Summary

• Clinical Project Management
• Investigator Recruitment and Qualification
• Negotiation of clinical study agreements and budgets
• Site start-up activities
• IRB Submissions
• Site Monitoring
• Quality Assurance and Auditing
• Regulatory Compliance
• Adverse Event Reporting
• Drug Shipment
• Central Lab Coordinator
• Study Close-out
• Data Management
• Study Reports
• Medical Writing
• Regulatory Submissions
• Investigators' Meetings
• Advisory Board Meetings
• Consultant Meetings

Adaptability

• Customize reports
• Flexible schedules
• Accommodate changes in project scope