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Primary screening allows direct high throughput binding measurements of small compounds without the need for labeling. However, mistakes about target-compound binding usually occur during primary HTS screening. In this role, Creative Biolabs serves an efficient secondary screening platform as complements to HTS assays.
The Precision in Drug Discovery Preclinical event will be a unique platform for the largest bio-pharmaceutical hub in the region to network and discuss collaboration in order to achieve their discovery and scientific strategies.
Drug screening is the process by which potential drugs are identified and optimized before selection of a candidate drug to progress to clinical trials. It can involve screening large libraries of chemicals for a particular biological activity in high-throughput screening assays.
The process begins with the identification of a disease or a therapeutic area with an unmet need. Once a druggable target is found, the process of drug screening starts. In drug screening, molecules that can interact with the target and/or facilitate the desired phenotypic response are identified.
What is the drug candidate selection process ? Drug candidate selection is the process of identifying potential new drugs that can be developed to treat a specific disease. This process involves several stages, including target identification, lead discovery, lead optimization, and preclinical testing.
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Historically, new drugs have been discovered through the random screening of active ingredients from natural sources and then validation of the hits for activity in animal models. Screening, as the name implies, is a sifting process to find the few compounds in a large set that have a desired biological activity.

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