Lovelace Scientific Resources
Lovelace Scientific Resources (LSR) is an independent clinical trials company dedicated to high-quality clinical trial performance. Headquartered in Albuquerque, New Mexico, LSR collaborates with a network of clinical trial sites throughout the United States. The company aims to improve health through clinical research, serving both patients and sponsors with a focus on safety, data quality, and effective patient recruitment.
Industries
Nr. of Employees
small (1-50)
Lovelace Scientific Resources
Products
Custom clinical trial database
A centralized database system used across sites to track participant flow, recruitment metrics, disease status and provide data for feasibility and trial management.
Clinical Trial
Independent clinical trials company services providing centralized services and collaborating with a network of clinical trial sites throughout the United States for study performance.
Clinical Trial Participant Enrollment
Clinical trial participant recruitment and enrollment services connecting interested individuals with clinical research opportunities.
Custom clinical trial database
A centralized database system used across sites to track participant flow, recruitment metrics, disease status and provide data for feasibility and trial management.
Clinical Trial
Independent clinical trials company services providing centralized services and collaborating with a network of clinical trial sites throughout the United States for study performance.
Clinical Trial Participant Enrollment
Clinical trial participant recruitment and enrollment services connecting interested individuals with clinical research opportunities.
Services
Full conduct of sponsored clinical trials at networked investigative sites, including protocol implementation, participant visits and clinical assessments.
Identification, screening and enrollment of eligible participants using dedicated recruiters and in-house advertising to support timely enrollment.
Provision of a custom database system to track participants, recruitment, disease status and to produce data for feasibility and sponsor reporting.
Support for regulatory oversight including document filing, trial master file maintenance, regulatory document review and compliance with FDA/ICH standards.
QA services to perform audits, ensure data integrity and meet sponsor timelines and deliverables.
Provision and management of clinical site equipment and infrastructure including ECG, PFT, centrifuges, scales, and secure investigational product storage.
Full conduct of sponsored clinical trials at networked investigative sites, including protocol implementation, participant visits and clinical assessments.
Identification, screening and enrollment of eligible participants using dedicated recruiters and in-house advertising to support timely enrollment.
Provision of a custom database system to track participants, recruitment, disease status and to produce data for feasibility and sponsor reporting.
Support for regulatory oversight including document filing, trial master file maintenance, regulatory document review and compliance with FDA/ICH standards.
QA services to perform audits, ensure data integrity and meet sponsor timelines and deliverables.
Provision and management of clinical site equipment and infrastructure including ECG, PFT, centrifuges, scales, and secure investigational product storage.
Expertise Areas
- Clinical trial management
- Participant recruitment and retention
- Clinical data management
- Regulatory compliance (FDA/ICH)
Key Technologies
- Custom clinical trial database / clinical trial management system
- Electronic and hardcopy document management systems
- Electrocardiography (ECG) equipment
- Pulmonary function testing equipment
News & Updates
Listing of ongoing trials including asthma, colorectal cancer, and other studies.
Listing of ongoing trials including asthma, colorectal cancer, and other studies.