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Pharmaceutical Articles & Analysis: Older
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Disease Modeling: Knockin cell lines mimic human disease conditions by introducing disease-related genetic mutations, thus offering a robust platform to study pathophysiology and screen potential therapeutic interventions. Pharmaceutical Development: These cell lines are essential in the drug discovery pipeline, allowing for high-throughput screening and functional assays to ...
Consequently, GPCRs have become a central focus in pharmaceutical research, serving as a target for a substantial percentage of modern therapeutic drugs. ...
In the realm of biotechnology and pharmaceuticals, stable cell lines serve as a foundation for producing high-yield protein therapeutics, monoclonal antibodies, and vaccines. ...
Benefits to Drug Development The implementation of CiPA translational assays offers numerous advantages to the pharmaceutical industry: Enhanced Safety Profiles: By providing a more accurate assessment of cardiac risks, CiPA helps ensure that only the safest compounds progress through the drug development pipeline. ...
These biological drugs have shown promise due to their effectiveness at low doses and relatively mild side effects compared to traditional pharmaceuticals. Currently approved cytokine-based drugs include various forms of interferons (such as IFN-α, IFN-β, IFN-γ, and IFN-ε), erythropoietin (EPO), granulocyte-macrophage colony-stimulating factor (GM-CSF), ...
In vitro permeability assay kits play a crucial role in the field of pharmaceutical development, particularly when evaluating the absorption characteristics of drugs. ...
These lab-created sequences of amino acids mimic naturally occurring peptides and are instrumental in advancing scientific discoveries and pharmaceutical innovations. This article delves into the basics of synthetic peptides, their synthesis, applications, and the future potential they hold. ...
In the ever-evolving world of pharmaceutical development, the quest to innovate and improve the delivery of drug substances remains a top priority. ...
It has qualified in recent years to analyze pharmaceuticals. The United States Pharmacopeia-National Formulary (USP-NF, US Pharmacopeia (USP)), the driving standardization body for (bio)pharmaceutical products, increased IC's potential during their modernization approaches, establishing it as an appropriate and valid technique in their compendial General ...
ByB&W Tek
The data obtained from the polarimeter is compared with reference data to understand the optical properties of the sample.MtoZ Biolabs provides customers with drug quality research services that comply with global pharmaceutical regulations. Based on the bioproduct physicochemical analysis and structural characterization analysis experimental platform, we provide you with ...
Creative Bioarray's reporting complies with FDA and EMA regulatory requirements for pharmaceuticals for human use (ICH Guidelines Q5B and Q5D, CTD Quality ...
These transformed bacterial strains can be deployed for the production of desirable products, such as biofuels, plastics, or active pharmaceutical ingredients, making the processes more efficient, sustainable and cost-effective. ...
Gene delivery is a therapeutic strategy that’s revolutionizing biotechnology and pharmaceuticals. It involves the delivery of new genetic molecules into target cells to treat diseases. ...
Clinical trials are the backbone of modern medicine, responsible for bringing innovative, safe, and efficient treatments to market after rigorous testing and evaluation. However, the conventional process of conducting these trials has often been long, expensive, and fraught with inefficiencies¹. The advent of predictive analytics is reshaping the landscape of clinical trials, ushering in a ...
Medical advancement relies on clinical trials, which are essential for the development of safe and effective innovative treatments. However, the success and general applicability of these treatments heavily depend on the diversity of the participants involved¹?³. This blog explores the importance of achieving data diversity in clinical trials to enhance clinical trial results and ...
Enantiomeric Purity and Chiral Drug AnalysisOptical activity analysis is the standard method in the pharmaceutical industry for determining the enantiomeric purity of drugs. ...
The high throughput and convenience of ultraviolet spectroscopy make it an ideal choice for early screening in drug development and quality control in the production process.MtoZ Biolabs provides drug quality research services that comply with global pharmaceutical regulations, including one-stop antibody drug ultraviolet spectroscopy analysis services.Antibody Drug Ultraviolet ...
In this edition of PHILOS Newsletter "Industrial Applications of Membrane Humidifier - Pharmaceutical and Semiconductor Industry", we explore in-depth how these membranes are pivotal in pharmaceutical manufacturing and semiconductor production, highlighting their importance and specific ...
Therefore, the HCP testing methods for each new product usually need to be developed and validated individually.Through precise and sensitive HCP host protein residual detection, pharmaceutical companies can ensure the safety and effectiveness of their products, thereby meeting regulatory requirements and protecting patient health.HCP Residual Detection: Ensuring ...
Pharmacokinetic and Toxicokinetic studies offer a valuable assessment tool in drug development and toxicology, providing crucial insights into the design, interpretation, and regulatory aspects of the chemical and pharmaceutical industry. Clearly, the harmonious dance between pharmacokinetics and toxicokinetics is the linchpin of safety assessment and therapeutic relevance in the ...