Scientists reviewing pharmacokinetic and toxicology data in a modern preclinical laboratory

Preclinical Drug Development

Preclinical drug development built for confident IND-enabling decisions.

For 80 years, Lovelace Biomedical has partnered with pharmaceutical, biotech, government, and academic innovators as a full-service, not-for-profit preclinical CRO — advancing novel therapies from discovery and proof-of-concept through IND-enabling toxicology, pharmacology, and bioanalytical programs.

80 yrsLeadership in preclinical science
375,000 ft²Single-site, bio-secure campus
500+Scientists & professionals on-site
6Core disciplines under one roof
Not-for-profit mission-driven CRO AAALAC-accredited animal facilities ABSL-3 containment laboratories Non-GLP through GLP full-spectrum IND support Albuquerque, NM · Est. 1947

The Lovelace Advantage

One scientific team, six disciplines, one roof.

Lovelace Biomedical is a full-service, not-for-profit preclinical CRO advancing novel therapies from discovery and proof-of-concept through IND-enabling studies. We partner with pharmaceutical, biotech, government, and academic innovators as true collaborators — focused on scientific impact, not stock price.

  • Full spectrum IND support, non-GLP through GLP
  • Custom solutions for complex, off-the-shelf-defying science
  • Deep translational expertise across 100+ disease models
  • Agile by design — fast proposals, real-time study adaptation
  • Non-profit, mission-driven leadership — not shareholder pressure
  • True scientific partnership aligned with your goals
Scientist preparing a dosing formulation at an analytical chemistry lab bench Formulation & dosing lab

Deep Experience, Powerful Capabilities

Six core disciplines. One integrated program.

Draw on individual capabilities or build a fully integrated preclinical package around a clear scientific and regulatory strategy — from first feasibility study to a submission-ready IND package.

01

Toxicology

80 years of exploratory to GLP-compliant regulatory toxicology across small and large species, with on-site QA and continuous GLP compliance since 1984.

02

Bioanalytical/Biomarker & Analytical Chemistry

Method development, validation, and sample analysis with specialized laboratory support for regulated and exploratory programs alike.

03

Formulation & Dosing

Simple to complex formulations enabling IV, IM, inhalation, intrathecal, intracerebral, ocular, and other specialized administration routes.

04

PK/TK & Biodistribution

Comprehensive characterization including radiolabeling, metabolite tracking, and modeling to connect exposure to safety and efficacy findings.

05

Pharmacology

Expertise in 100+ animal models spanning respiratory, CNS, infectious disease, radiation injury, and other therapeutic areas.

06

Animal Welfare

Extensive vivarium capacity supporting short- and long-term housing for small and large species on one bio-secure campus.

The Development Pathway

From target to IND — mapped to where Lovelace adds the most value.

We start where discovery ends. Lovelace becomes your core scientific partner from bioanalytical and biomarker development through your completed IND-enabling package — while staying ready to provide guidance on earlier discovery-stage work when your program needs it.

Lovelace Biomedical development pathway diagram. Discovery and lead optimization stages (target identification and validation, hit identification and screening, lead optimization, in vitro NAM ADME and safety) are typically sponsor-led. Lovelace's core pathway then covers bioanalytical and biomarker/analytical development, PK-PD and biodistribution, preliminary toxicology studies, GLP toxicology studies, and safety pharmacology as key LBRI areas; repro/genotox as needed; and CMC and formulation plus the IND-enabling package as areas of selective support.

Lovelace Biomedical's development pathway overview. Scroll to explore the full diagram →

Tackling Pharma's Biggest Challenges

Deep experience in the therapeutic areas that resist off-the-shelf models.

Decades of translational and disease-model expertise let us design studies for programs that don't fit standard preclinical playbooks.

Respiratory

Global leader in inhalation toxicology and aerosol science. Custom exposure systems across asthma, COPD, acute lung injury, and inhaled therapeutics.

Infectious Disease

Complex, high-containment studies in ABSL-3-enhanced labs, aerosol challenge models, select-agent and high-containment expertise.

Gene-Cell Therapy

A decade of AAV/vector toxicology, 25+ NIH-supported IND-enabling studies, and advanced dosing expertise.

Neuroscience

Integrated behavioral research and advanced imaging through Mind Research Network collaboration.

Medical Countermeasures

CBRNE threat expertise and Animal Rule study support for programs with no traditional efficacy pathway.

Alternative Tobacco & Nicotine

25+ years studying health effects and public health impact of novel nicotine and tobacco products.

Inside the Facility

One bio-secure campus, built for multi-species preclinical science.

"All core capabilities under one roof — histopathology, clinical pathology, analytical & bioanalytical chemistry, microbiology & virology, cell & molecular biology, safety pharmacology, and toxicology — with embedded scientific leadership enabling rapid communication and execution."
Lovelace Biomedical, Company Overview
  • Facility footprint375,000+ sq ft
  • Secure campus100+ acres, Kirtland AFB
  • GLP complianceContinuous since 1984
  • Professionals on-site250+, incl. 50+ PhDs/DVMs/MDs
  • Animal rooms93, multi-species capability
  • AccreditationAAALAC-accredited, OLAW-assured, USDA-registered
Interior corridor of Lovelace Biomedical's animal housing facility, lined with secure caging on both sides and staff performing husbandry care Animal housing & welfare ecosystem

Multi-Species Capability

Non-human primate, swine, sheep, dog, ferret, rat, guinea pig, rabbit, and rodent housing across 93 dedicated animal rooms (includes European style).

ABSL-3 High-Containment

10,000+ sq ft of enhanced containment space with multi-species support, fully GLP-compliant with on-site QA.

Fully Integrated On-Site Support

Surgical suites, clinical pathology, histopathology, and large & small animal necropsy, all under one roof.

Dedicated Animal Welfare Resources

A behavioral management program, lab animal medicine, and a specialty food-grade enrichment kitchen.

Guided by Purpose

A not-for-profit partner, built around scientific integrity.

Our mission shapes how every program is designed, staffed, and delivered — as a partner invested in your outcome, not a vendor billing by the hour.

Not-for-Profit, Science-First

Driven by science, quality, and integrity — not shareholder pressure or stock price.

Ethical Animal Welfare

Responsible, compliant animal care treated as a scientific and ethical priority, not a checkbox.

Scientific & Ethical Leadership

Integrity embedded in every study design, execution decision, and report we deliver.

Collaboration & Transparency

Open partnership as a cornerstone of every program, aligned with your goals from day one.

Powered by Our People

Multidisciplinary teams driving innovative, thoughtful, and impactful solutions for your program.

Frequently Asked

Questions programs ask before their first study.

Both. Sponsors can draw on individual capabilities — a single PK study or a GLP toxicology program — or build a fully integrated package spanning bioanalytical development, toxicology, safety pharmacology, and CMC/formulation support, sequenced toward a submission-ready IND.
Yes. We design non-GLP pilot and feasibility studies alongside full GLP toxicology programs, sequencing both to generate decision-ready data as your program advances toward IND, NDA, or BLA submission.
Our scientists work across 100+ animal models of disease, with particular depth in respiratory disease, infectious disease and high-containment work, gene and cell therapy, neuroscience, and medical countermeasures — alongside general and specialty toxicology for any indication.
Yes — histopathology, clinical pathology, analytical and bioanalytical chemistry, and formulation and dosing support all run on-site alongside toxicology and pharmacology, so exposure, safety, and pathology findings stay connected under one operational plan.

Bring us your preclinical program.

Our scientific team can help shape an efficient, decision-driven plan for your next exploratory or IND-enabling study.