The Importance of Pharmaceutical ADME Studies
Pharmaceutical ADME studies are designed to investigate how a chemical is processed by an organism.
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Pharmaceutical ADME studies are designed to investigate how a chemical is processed by an organism.
This expert Q&A session from PharmaPlanter's founder explores the importance of these efforts in producing reliable results. In PharmaPlanter, Dr Cheng turned his expertise in gene-editing and bio-modeling into an efficient and cost-effective technology...
Researchers, developers, and manufacturers must remain adept at utilizing both small and large molecule approaches, leveraging their unique advantages to address unmet medical needs.
Discover how toxicology testing protects human health, supports regulatory approval, and promotes innovation across various industries
Pharmacogenetics is a branch of science that studies how a person's genetics influence their response to pharmaceuticals (read an entry to pharmacogenetics, here). Adverse Drug Reactions (ADRs) are one of the biggest influences in the study of pharmacogenetics, as...
Need a laboratory for cancer research? Today, the US National Science Foundation issued a Press Release that the New York University Tandon School of Engineering has created a new synthetic hybrid molecule that delivers a blow to breast cancer cells. The hybrid...
Discover how these assays support regulatory compliance, product development, and batch consistency in the biotech industry.
Biological products comprise a wide array of products, all of which are regulated in the US by FDA's CBER (Center for Biologics Evaluation and Research) division and include regulation of blood, blood components, bioassays biosmiliars, biobetters, and...
Potency testing is a term used to describe the process of measuring biological activity in a product. Many methods exist to determine the potency of a biopharmaceutical such as ligand and receptor binding assays, cell culture-based assays, and animal-based assays....
Pharmacogenetics is the study of how genetic differences affect a person's response to medicine. Pharmacogenetics is often used interchangeably with pharmacogenomics. Pharmacogenetic research and testing determine a person's ability to metabolize medicines and...
What is CCIT? Container Closure Integrity Testing (CCIT) is done to evaluate the strength and integrity of a container closure system. Testing of container closures is important as it ensures a sterile barrier against microorganisms and other potentially dangerous...
The drug development process is an iterative process. Each stage of development helps to ensure the final product is effective and safe. Preclinical drug development, often called preclinical studies, is the stage in the drug development process where the safety of...
Compounding pharmacies are pharmacies that create personalized medications by mixing ingredients based on a doctor's prescription in an effort to meet a person's needs. Though compounding pharmacies lost popularity in the 50s and 60s when mass drug manufacturing...
Pharmaceutical Drug Development is an extremely long and very costly process. However, pharmaceutical drug development is made faster through new software known at AptaTRACE. AptaTRAC was developed by scientific researchers led by Dr. Teresa Przytycka of the US...
Most drug toxicology testing is performed on urine samples, as most drugs are broken down and excreted through urine. Testing can also be done on blood, however, concentrations of drugs are usually higher in urine and testing is less invasive, faster, and cheaper....
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Quality management is a cornerstone of successful business operations in the...
The US RPTA Guideline (Regulated Product Testing and Analysis) is a pivotal...
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