Advantages Of Hiring LC-MS/MS Analysis Lab For Your Therapeutic Peptides - LC-MS/MS quantification of therapeutic peptides has become a routine quantification in the drug development space. Hiring an LC-MS/MS analysis lab for the evaluation of therapeutic peptides is advantageous over performing them in less skillful environments.

Importance of High-Quality Reference and Internal Standards in HPCL MS Method - Reference standards are calibration solutions that help compare the response of an LC-MS/MS instrument obtained while evaluating an unknown sample against a sample whose concentration is known. https://bit.ly/3qKXXE1

HPLC Method Development For Drugs And Biomarkers - The pharmaceutical industry needs robust bioanalytical methods such as HPLC. The HPLC method development ensures that the chromatography technique is optimized for carrying out experiments in the discovery and development of pharmaceutical drug products. https://bit.ly/3nqnMXU

HPLC Testing In Early Nonclinical Drug Development Workflows - HPLC analysis is one such essential testing modality that has been employed over and over in the drug development process. HPLC testing involves a lot of critical steps. HPLC testing has become a cornerstone technique in nonclinical and clinical research. https://bit.ly/3npH6EQ

What Are ADME Studies? ADME are the four steps of pharmacokinetics, used in the drug development process to investigate numerous factors that influence drug action and effectiveness. The evaluation of these pharmacological properties is critical for the selection of a new drug candidate during drug discovery and development. Learn more about What Are ADME Studies? https://www.nebiolab.com/adme-studies/

Drug Metabolism And Pharmacokinetics Drug metabolism and pharmacokinetics (DMPK) is a core discipline in drug development that considers the biotransformation of a drug compound and other pharmacokinetic properties to assess drug safety. DMPK, or commonly referred to as DMPK, is a scientific discipline within drug discovery, dealing with safety and efficacy evaluation of drug candidates before entering clinical trials. https://www.nebiolab.com/drug-metabolism-and-pharmacokinetics-dmpk/

Should You Partially Or Fully Validate Your Biomarker Assay - FDA biomarker validation guidelines suggest that the validation criteria should revolve around the intended use of a biomarker and the certainty with which it can resolve the intended use. Regulatory guidelines expect biomarker validation to be a continuous process where it is regularly tailored and updated as new data and information are obtained through preclinical and clinical studies. https://gopoco.us/Should_You_Partially_Or_Fully_Validate_Your_Biomarker_Assay/MjM4NQ==

Why Reliance on Biomarker Testing Services Has Increased To Support Clinical Endpoints? - Bioanalytical laboratory have understood that their success in developing potential candidates skyrockets once they display proof of concept. A focused approach employing the best scientific practices is the primary focus of all bioanalytical laboratories. Such an approach has seen increasing use of biomarker testing services. https://tananet.net/why-reliance-on-biomarker-testing-services-has-increased-to-support-clinical-endpoints/