The network of Lovelace Scientific Resources’ clinical sites function independently so sponsors can select one or all sites to conduct a clinical trial. Practices common to conducting trials at all LSR sites include:

• Affiliation with private practice physician investigators
• Use of standardized operating procedures
• Dedication of Good Clinical Practices
• Centralized budgets and contracts
• In-house advertising develpment and placement
• Regulatory supervision and compliance
• Librarian services for collation and storage of all records at our privately owned corporate office site

Lovelace Scientific Resources’ custom database software is used at all sites to manage information flow. The system is used in trial management for the following activities:

• Tracking study participants from initial contact to trial completion
• Tracks patient recruitment
• Identifying participant disease status for all enrolling trials
• Providing data to determine feasibility for future trials