nebiolab's Updates (64)
-
-
Liquid Chromatography-Mass Spectrometry is one of the most used techniques for small molecule bioanalysis. In this blog we will study some of the crucial aspects that the FDA truly cares about. https://zumashare.com/2021/06/15/lc-ms-ms-testing-miss-the-big-picture-stuff-that-fda-cares-about/ [more]
-
-
A robust bioanalytical assay and its validation provide quantitative information related to xenobiotics and biotics in a biological system. Read more https://www.fuzia.com/article_detail/239256/bioanalytical-assays-for-drug-development [more]
-
-
Bioanalytical method development and validation are essential for defining the parameters of human clinical pharmacology, bioequivalence studies, bioavailability, pharmacokinetic evaluation, toxicology studies, non-human pharmacology, and preclinical studies. https://tagbookmarks.info/why-does-biotech-invest-in-bioanalytical-method-development-and-validation/ [more]
-
-
-
Bioavailability and bioequivalence studies provide useful information about the availability of safe and effective pharmaceutical drugs to patients and medical practitioners. Here are the benefits of setting up bioavailability assay. https://www.vingle.net/posts/3717921 [more]
-
-
Biomarkers play an important role in disease identification and have now gained a more comprehensive role in drug discovery and development. Read this blog to know more about available biomarker assay for cerebrospinal fluid. https://newshubfeed.com/category/health/what-are-the-commercially-available-biomarker-assay-for-cerebrospinal-fluid-csf [more]
-
-
Bioanalytical services play an important role in the drug development process. Their expanded role encompasses several facets, including the selection of a drug candidate and carrying out clinical trials. Here are the top solid reasons to partner with bioanalytical CRO. https://hazelnews.com/why-do-you-need-to-partner-with-an-excellent-bioanalytical-cro-today/ [more]
-
-
Biomarkers are taking a prominent role through drug discovery to clinical trials and quality assurance. Advances in scientific technology, molecular characterization, etc. https://buzztum.com/biomarker-assay-development-validation-for-quantitative-proof-of-concept-poc/ [more]
-
-
In vivo studies are usually preferred for oral immediate-release products, non-oral immediate-release products, and modified-release products. Read more https://gumroad.com/nebiolab/p/overview-of-in-vitro-and-in-vivo-bioequivalence-testing-services-for-your-anda-submission [more]
-
-
HPLC testing services perform qualification at startup of the instrument, when relocating or reinstalling, after repair or maintenance, or as a regular performance check. Here the reasons to use hplc testing. https://wolfensteincenter.com/2021/04/16/why-do-we-use-hplc-testing-to-determine-stability-in-dosing-wehicle-formulation/ [more]
-
-
Bioequivalence studies of generic drug products are considered surrogate measures for FDA approval. Read this blog to to know the challenges faced by Bioequivalence studies during covid-19. https://kwirmedia.com/covid-19-challenges-and-mitigation-for-your-bioequivalence-study-testing/ [more]
-
-
Meso Scale Discovery is a platform to develop immunoassays that measure biomarkers in biological research and pre-clinical and clinical trials. Read more to find most popular preclinical and clinical meso scale discovery panels. https://blog.storymirror.com/read/bp5py3o0/what-the-most-popular-preclinical-and-clinical-meso-scale-discovery-panels [more]
-
-
Bioequivalence is the core component of generic drug testing. Bioequivalence studies act as a surrogate marker for safety and clinical data. Read this blog to know how to design bioequivalence studies. https://www.atoallinks.com/2021/how-to-design-your-bioequivalence-studies-for-rapid-progression-and-approval/ [more]
-
-
Copyright 2019 © P-tweets Refunds