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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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• Pharmacokinetic assay study design is a valuable approach for biologics integrating quantitative information about a drug’s pharmacological properties of a pharmaceutical drug candidate. https://www.bingarticles.info/pk-assay-development-for-biologics-using-elisa-msd-immunoassay-platforms/. [more]

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• Bioequivalence assay requirements are designed before clinical trials because bioequivalence studies are crucial for the determination of various products with active ingredients being marketed under different licenses. https://www.guest-articles.com/health/ask-the-experts-popular-bioequivalence-assay-platforms-for-clinical-development--29-11-2020. [more]

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• LC MS is one of the most used techniques for small molecule bioanalysis. LC-MS is a crucial technology for the quantification of small molecules in drug development. Read more to know how lc ms analysis is different from hplc sample analysis. https://www.knowpia.com/s/blog_5ad705a1fb929573. [more]

  by nebiolab, Health,

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• Bioequivalence is necessary to reflect the comparability of two drug products using the same therapeutic substance. Read more to find the importance of bioequivalence clinical trial transparency for drug development. https://shortkro.com/importance-of-bioequivalence-clinical-trial-transparency-for-drug-development/. [more]

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