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DNA microarrays, also known as gene chips, are powerful tools used in molecular biology to analyze gene expression and genetic variations. This article delves into the importance of DNA microarrays, their applications, and the technology behind them.
Learn about the importance of extractables and leachables (E&L) testing in pharmaceuticals. This guide covers the testing process, regulatory guidelines, and best practices to ensure drug safety, quality, and compliance with industry standards.
Epigenetics is the study of changes or variations in gene expression that are caused by external factors switching the genes on and off, ultimately affecting how they are expressed. Epigenetic changes occur naturally though they can be influenced by age, lifestyle,...
Toxicology research and testing are critical components of ensuring the safety and efficacy of chemicals, pharmaceuticals, and consumer products. This discipline involves the study of the adverse effects of chemical substances on living organisms and the...
Monoclonal antibodies (mAbs) are lab-made proteins that mimic the immune system's ability to fight off harmful pathogens.
By fostering partnerships and promoting a culture of innovation, translational science has the potential to transform healthcare and improve the lives of millions of people around the world.
Sterility Assurance Level (SAL) is a crucial measure used in the sterilization of medical devices, pharmaceuticals, and other products to ensure they are free from viable microorganisms. Achieving an appropriate SAL is essential for the safety and efficacy of...
FDA compliance in veterinary medicine testing is not only a regulatory requirement but also a benchmark for quality and safety in animal health products. Ensuring the safety and efficacy of veterinary drugs, devices, and food additives is a top priority that...
By using advanced analytical methods such as HPLC, GC-MS, LC-MS, FTIR, and NMR, pharmaceutical companies can accurately identify and quantify controlled substances, verify product quality, and meet regulatory standards.
ISO 10993 medical device biocompatibility testing is performed to observe how compatible a device is with living tissue. To be considered biocompatible, a device needs to cause no local or systemic response. Biocompatibility is determined through a series of tests...
U.S. Pharmacopeia (USP) is an organization whose main goal is to help improve human health by creating standards to ensure higher quality and safer pharmaceuticals, foods, and dietary supplements (learn more about USP standards). The FDA enforces standards set by...
DNA fingerprinting is a revolutionary technique that allows us to identify individuals based on their unique genetic makeup. This article delves into how DNA fingerprinting works, its applications, and its significance in fields like forensics, paternity testing, and genetic research.
Pharmaceutical particle size analysis is a fundamental aspect of drug development, manufacturing, and quality control.
Scientific research relies on a variety of testing methods to understand biological processes, develop new treatments, and ensure the safety of products
Genetic markers are specific sequences of DNA that can be used to identify individuals, populations, or traits of interest. This guide explores the various types of genetic markers, their applications, and their importance in genetics, medicine, and evolutionary biology.
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