Noble Life Sciences
Noble Life Sciences is a comprehensive preclinical contract research organization dedicated to advancing scientific knowledge and therapeutic development. They offer a wide range of services including drug, device, and biologic development phases, with expertise in toxicology, efficacy, pharmacokinetics, and bioanalysis. Their mission is to support biotech, pharmaceutical, and medical device companies in bringing innovative therapies to market efficiently and safely. Noble is equipped with state-of-the-art facilities and a team of experienced scientists, veterinarians, and support staff committed to ethical research and scientific excellence. They also provide specialized models such as humanized mice for immunotherapy research, and advanced imaging services for preclinical studies.
Industries
Nr. of Employees
small (1-50)
Noble Life Sciences
Products
Toxicology Services
GLP and non-GLP preclinical contract services including exploratory toxicology, general toxicology, immunotoxicology, and reproductive toxicology.
GLP Toxicology Services
Comprehensive GLP and non-toxicology testing services including exploratory toxicology, general toxicology, immunotoxicology, and reproductive toxicology to support IND, IDE, or PMA FDA submissions.
Orthotopic Tumor
Preclinical oncology research service featuring organ-specific tumor implantation to study tumor progression, metastasis, and therapeutic responses in a biologically relevant microenvironment.
Orthotopic Tumor Model Services
Preclinical oncology research services utilizing orthotopic mouse models for tumor implantation in organ-specific sites to closely mimic the human disease state.
Cell line-derived
In vivo tumor models using human cancer cell lines designed for rapid, reproducible, and scalable drug screening.
Cell line-derived xenografts (CDX models)
Reproducible tumor models for robust data.
Toxicology Services
GLP and non-GLP preclinical contract services including exploratory toxicology, general toxicology, immunotoxicology, and reproductive toxicology.
GLP Toxicology Services
Comprehensive GLP and non-toxicology testing services including exploratory toxicology, general toxicology, immunotoxicology, and reproductive toxicology to support IND, IDE, or PMA FDA submissions.
Orthotopic Tumor
Preclinical oncology research service featuring organ-specific tumor implantation to study tumor progression, metastasis, and therapeutic responses in a biologically relevant microenvironment.
Orthotopic Tumor Model Services
Preclinical oncology research services utilizing orthotopic mouse models for tumor implantation in organ-specific sites to closely mimic the human disease state.
Cell line-derived
In vivo tumor models using human cancer cell lines designed for rapid, reproducible, and scalable drug screening.
Cell line-derived xenografts (CDX models)
Reproducible tumor models for robust data.
Services
End-to-end preclinical services including study design, execution of in vivo efficacy and safety studies, GLP toxicology, PK/PD, histopathology and regulatory-directed data generation.
DNA/RNA isolation from tissues and fluids, absolute copy-number quantification, transgene expression analysis, assay development and validation, and GLP-compliant reporting for cell and gene therapy programs.
High-sensitivity absolute quantification services using digital PCR for mutation/pathogen detection, copy-number analysis, viral titer measurement and residual host-cell DNA assays with high daily throughput.
Longitudinal in vivo imaging including bioluminescence/fluorescence imaging for molecular endpoints and anatomical/interventional imaging support such as fluoroscopy, radiography and ultrasound for procedural and anatomical endpoints.
Services to generate humanized mice via CD34+ HSC engraftment in immunodeficient strains, longitudinal chimerism monitoring and immune lineage phenotyping by flow cytometry.
Preclinical testing of adhesion barriers and soft tissue grafts using standardized surgical adhesion models, histology/IHC, and biomechanical assessments (uniaxial tension, suture retention, ball-burst) to evaluate handling, strength and resorption.
End-to-end preclinical services including study design, execution of in vivo efficacy and safety studies, GLP toxicology, PK/PD, histopathology and regulatory-directed data generation.
DNA/RNA isolation from tissues and fluids, absolute copy-number quantification, transgene expression analysis, assay development and validation, and GLP-compliant reporting for cell and gene therapy programs.
High-sensitivity absolute quantification services using digital PCR for mutation/pathogen detection, copy-number analysis, viral titer measurement and residual host-cell DNA assays with high daily throughput.
Longitudinal in vivo imaging including bioluminescence/fluorescence imaging for molecular endpoints and anatomical/interventional imaging support such as fluoroscopy, radiography and ultrasound for procedural and anatomical endpoints.
Services to generate humanized mice via CD34+ HSC engraftment in immunodeficient strains, longitudinal chimerism monitoring and immune lineage phenotyping by flow cytometry.
Preclinical testing of adhesion barriers and soft tissue grafts using standardized surgical adhesion models, histology/IHC, and biomechanical assessments (uniaxial tension, suture retention, ball-burst) to evaluate handling, strength and resorption.
Expertise Areas
- Preclinical in vivo model design and execution
- GLP toxicology and IND-enabling study support
- Cell and gene therapy biodistribution and molecular quantification
- Digital PCR and high-sensitivity nucleic acid quantification
Key Technologies
- Digital PCR (dPCR) with high-throughput nano-partitioning
- Quantitative PCR (qPCR) and RT-qPCR
- Next-generation sequencing (NGS)
- Multicolor flow cytometry and FACS
News & Updates
Mar 16 – 20, 2025. Noble Life Sciences to exhibit at the Society of Toxicology annual meeting.
Nov 17 – 20, 2024. Noble Life Sciences to attend the American College of Toxicology annual meeting.
Jun 10 – 11, 2024 in Boston, Massachusetts. Noble Life Sciences participates in the summit.
May 7 – 11, 2024 in Baltimore, MD. Noble Life Sciences to participate.
Apr 5 – 10, 2024 in San Diego, CA. Noble Life Sciences to present at the conference.
Apr 3, 2024. An online event discussing regulatory strategies.
Mar 16 – 20, 2025. Noble Life Sciences to exhibit at the Society of Toxicology annual meeting.
Nov 17 – 20, 2024. Noble Life Sciences to attend the American College of Toxicology annual meeting.
Jun 10 – 11, 2024 in Boston, Massachusetts. Noble Life Sciences participates in the summit.
May 7 – 11, 2024 in Baltimore, MD. Noble Life Sciences to participate.
Apr 5 – 10, 2024 in San Diego, CA. Noble Life Sciences to present at the conference.
Apr 3, 2024. An online event discussing regulatory strategies.