About Us
NorthEast BioLab is an independent bioanalytical contract research organization (CRO) that supports pharmaceutical and biotechnology companies in drug development. Since its founding in 2003, the company has provided bioanalytical services for the quantification of drugs, metabolites, and biomarkers, as well as support in the areas of clinical trial kitting and biosample storage. Its expertise includes pharmacokinetic (PK) and toxicokinetic (TK) studies, immunogenicity, biomarker analysis, and cell-based assays.
With GLP- and GCP-compliant processes and extensive experience in both preclinical and clinical studies, NorthEast BioLab supports clients throughout the entire drug development process. By combining scientific expertise with a flexible, project-oriented approach, the company delivers reliable bioanalytical data that contribute to well-informed research and development decisions.
Contact us
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35 Worth Ave, CT 06518
Hamden, United States
+12033613780
sales@nebiolab.com
Services
Explore our services and discover how we can support you. With a wide range of solutions, we help you address a variety of challenges, tailored to your organization.
Read what our customers say about us

We have worked with NorthEast BioLab for over ten years because of their commitment to the highest quality bioanalytical data.
Senior Associate Director, Clinical Trials
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Policy documents
We are part of the Normec Group.
Normec is a leading organization in the TICC sector (Testing, Inspection, Certification, Compliance). Our areas of expertise range from (drinking) water quality, air quality, and soil quality to fire safety, food safety, management systems, fair labor practices, good working conditions, and social compliance. Every day, we work to create a safe, healthy, and reliable work and living environment—for this generation and future generations.
Frequently Asked Questions
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A Bioanalytical CRO (Contract Research Organization) provides specialized laboratory services such as bioanalytical testing, method development, and validation for pharmaceutical and biotechnology companies. They play a crucial role in drug development by ensuring the safety and efficacy of new drug candidates.
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Partnering with a Bioanalytical CRO like ours ensures access to state-of-the-art laboratory facilities, expert scientific teams, and streamlined processes. This partnership can accelerate drug development timelines, reduce costs, and ensure regulatory compliance.
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We offer a comprehensive range of bioanalytical services, including method development and validation, pharmacokinetic and toxicokinetic studies, biomarker analysis, and more. Our state-of-the-art Bioanalytical CRO Lab supports various stages of drug development.
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As a leading Biotech CRO, we provide tailored bioanalytical and regulatory support to emerging biotechnology companies. Our services help optimize drug discovery and development processes, ensuring successful progression through clinical trials.
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With over 20 years of experience, we are a preferred Pharma CRO for many pharmaceutical companies. Our expertise in bioanalytical analysis, compliance with regulatory standards, and a proven track record of successful partnerships make us an ideal choice for pharmaceutical research and development needs.
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Our Bioanalytical CRO Lab is equipped with advanced technology and staffed by experienced scientists. We offer precise and reliable bioanalytical analysis CRO services, adhering to stringent quality control measures to meet the highest industry standards.
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CRO services provide specialized knowledge and infrastructure, enabling biotech and pharmaceutical companies to focus on core competencies. By outsourcing bioanalytical tasks, companies can achieve faster turnaround times, efficient resource utilization, and improved regulatory compliance, accelerating the drug development process.
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We specialize in a variety of bioanalytical analyses, including but not limited to, small and large molecule bioanalysis, biomarker analysis, immunogenicity testing, and pharmacokinetic studies. Our services cater to both early and late-stage drug development.
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Yes, we offer both GLP (Good Laboratory Practice) and non-GLP bioanalytical services. This flexibility allows us to support different stages of drug development, from early discovery through to regulatory submission.
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Flow cytometry is a laboratory-based technique that helps to analyze cells or cell components in a sample (suspended in a fluid) by measuring cell count and determining their physical and chemical characteristics. It finds extensive application as a research and diagnostic tool for diseases.