GLP Toxicology Services
Comprehensive GLP Toxicology Services
Lovelace Biomedical is a leading provider of GLP toxicology services, supporting pharmaceutical, biotechnology, academic, and government research clients across the United States. With over 70 years of scientific excellence and regulatory experience, we deliver rigorous, compliant studies that form the foundation of safe and effective drug development. Our team provides tailored toxicology programs designed to meet global standards while advancing your therapeutic pipeline efficiently and confidently.
Regulatory Expertise That Drives Development Forward
Our GLP toxicology programs are built on decades of regulatory knowledge and hands-on experience supporting IND, NDA, and BLA submissions. Lovelace Biomedical’s scientists ensure every study aligns with FDA, EPA, and OECD guidelines, offering full transparency and defensible data. From study design to submission-ready reports, we help sponsors navigate complex regulatory pathways with confidence.
Comprehensive GLP Toxicology Capabilities
Our 300,000 square feet of advanced laboratory facilities enable a wide range of GLP toxicology studies across multiple therapeutic modalities, including small molecules, biologics, and advanced therapies. We specialize in inhalation, genetic, and toxicokinetic testing programs, along with tissue-specific compound analysis and dosimetric evaluations. Each study is managed by cross-functional teams of toxicologists, pharmacologists, and pathologists who ensure precision and reproducibility at every stage.
IND-Enabling Studies That Accelerate Clinical Success
At Lovelace Biomedical, our GLP toxicology studies play a pivotal role in preparing IND-enabling data packages. We understand the urgency of moving promising therapies into the clinic, which is why our programs are designed to streamline timelines without compromising scientific integrity. Sponsors benefit from our comprehensive study documentation, transparent reporting, and collaborative communication throughout the process.
Specialized Facilities and a Culture of Collaboration
Our state-of-the-art facilities in Albuquerque, New Mexico, provide the controlled environments and advanced equipment necessary for complex GLP toxicology studies. Lovelace Biomedical’s collaborative culture ensures our sponsors stay informed at every stage of research. We integrate expertise across disciplines, from pharmacology and toxicology to pathology, delivering actionable data and meaningful insight that drive decision-making. Whether you are advancing a new oncology therapy or developing an innovative biologic, our dedicated team stands ready to support your success.
Contact Lovelace Biomedical for
GLP Toxicology Expertise
Your preclinical program deserves the support of a proven partner. Lovelace Biomedical combines decades of regulatory experience, advanced facilities, and scientific rigor to deliver industry-leading GLP toxicology services. Contact us today to discuss your study needs and discover how our team can help accelerate your path from discovery to clinical success.