Health & Medicine Insights

Powered by NorthEast Biolab, an ambitious group of healthcare investors and scientists brought together by shared passion for high-quality and innovative drug development and research.

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Why Choose Clinical Laboratory Services From NorthEast BioLab?

NorthEast BioLab has 15+ years experience in helping sponsors accelerate their clinical trial timeline. We offer clinical laboratory services in strict compliance with regulatory guidelines to positively impact the intended purpose of your clinical trials. We are a clinical research organization that can manage and monitor your complicated clinical studies seamlessly, utilizing our bioanalysis and project management expertise, skilled scientists, technicians, and managers, as well as latest equipment and state-of-the facility.

Thus, you can rely on NorthEast BioLab CRO services to advance your drugs with a shorter time to market, accurate efficacy and safety profile, and lower operational costs.

Source URL: https://www.nebiolab.com/clinical-cro/

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Method Validation Services at NorthEast BioLab

NorthEast BioLab test method validation services are extensive and adapt to the different phases of your drug development journey. 

For method validation, NorthEast BioLab offers a whole range of stringency levels so that the client can choose what they need. This generates an extremely comprehensive validation report that details the method being validated, as well as its outcomes. It also ensures that we report on the protocol used, calculations made, procedures followed, and equipment used.

Source URL: https://www.nebiolab.com/method-validation/

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What are ADME Studies?

The in vitro and in vivo ADME studies offer a deep understanding of Pharmacokinetic (PK) properties of the selected drug candidates. Assessing the potential of the compound in the early drug development phases offer desirable efficacy and safety profile of the drug candidate.

The assessment of ADME pharmacokinetics is critical for various stages of drug development, such as discovery, preclinical, and clinical phases. ADME and toxicity studies offer a clear knowledge of the metabolism and safety profile of a feasible drug candidate, enabling proper execution of clinical trials. However, it is necessary to conduct these studies in a controlled environment, which is why scientists rely on their industry knowledge and FDA approved standards for the in vivo and in vitro studies.

SOURCE URL: https://www.nebiolab.com/adme-studies/