nebiolab's Updates (64)
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Bioequivalence is the development of a generic drug version of an already existing brand name version and is necessary for drug development to test the efficacy of a drug. In this blog we will discuss how to improve success rate in expensive bioequivalence study. https://tananet.net/how-to-improve-your-success-rate-in-expensive-bioequivalence-studies/ [more]
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Bioanalytical method validation involves the optimization of both the process and conditions for extracting and detecting the analyte under consideration. Here is the comparison between the FDA guidance and EMA guideline. https://rewardbloggers.com/blog/post/16768/bioanalytical-method-validation-fda-guidance-vs-ema-guideline [more]
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ELISA stands for Enzyme-Linked Immunosorbent Assay. It is a qualitative as well as a quantitative immunological assay to determine antigen and antibody in a sample. In this blog we will compare ELISA with LC MS method for quantitative analysis of lipids. https://thewritters.com/comparison-of-elisa-with-lc-ms-ms-method-for-quantitative-analysis-of-lipids/ [more]
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Clinical biomarker testing services help us test the safety and efficacy of clinical interventions, understand the disease mechanisms, and make correct clinical decisions. Read the impact of clinical biomarker testing on drug development. https://snaptoad.com/critical-application-and-impact-of-clinical-biomarker-testing-on-drug-development/ [more]
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Pharmacokinetic study has always been an integral part of the research and development for all the novel therapeutic drugs till date. Read more https://www.ecogujju.com/define-pharmacokinetic-for-drug-efficacy/ [more]
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A bioanalytical laboratory uses biomarkers to identify the normal biological, pharmacological, and pathological processes in the human body. In this blog we discuss everything about Immuno-oncology drug development in a bioanalytical lab. https://airra.org/what-you-must-learn-about-immuno-oncology-drug-development-in-bioanalytical-laboratory/ [more]
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The process of clinical toxicological analysis begins with safety testing. At this stage, the drug's effects on different vital functions are evaluated. Read more https://em360tech.com/feed-board/ask-experts-glp-toxicity-study-layouts-and-assay-platforms-expedite-clinical-development [more]
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Preclinical toxicology studies come in the role of ensuring that the developed drug is safe for both humans and animals. The tox study is conducted on at least one rodent and one non-rodent species. Experts obtain the results, analyze them, and check if the medicinal product is safe for sale. [more]
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Pharmacokinetics definition states the concept as the study of a drug’s movement in a living body. Read more https://writeablog.net/3bj26ebd55 [more]
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Pharmacokinetics definition refers to PK assay as the study of a drug’s movement through the patients’ body. In pharmacokinetic testing, different biological fluids such as blood and plasma are analyzed. https://www.loomio.org/d/AePI9FYy/3-key-drivers-of-drug-design-metabolism-pharmacokinetics-and-toxicity [more]
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PK analysis studies the passage of the drug in the human body right from its absorption to its removal. PK analyses have a significant role to play in drug development, as explained in this blog. http://www.bubbledock.com/bioanalytical-pk-analysis-of-antibody-drug-conjugate-therapeutics/ [more]
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