Excipients

Pharmaceutical excipients, which can be functional or inactive ingredients, work to enhance the medically relevant properties of the API. When used to promote ingredient qualities, excipients can be an asset for formulators to increase stability, bulk up the formulation, or enhance the therapeutic effects of the API. Below you can explore helpful resources including editorial coverage and webinars related to pharmaceutical excipients.

  • Integrated Multi-Omic Data: Powering Precision Medicine

    Precision medicine is poised to transform medicine as we’ve known it, from the earliest R&D efforts by drug developers all the way to patient assessment and physician prescribing. In fact, it is projected that the precision medicine market will reach into the hundreds of billions of dollars in the coming years. But getting there presents some of ... read more

  • The Critical Role of Diagnostics in Antimicrobial Stewardship

    Antimicrobial resistance (AMR) is a pressing global health challenge. While much of the discussion is focused on future implications, resistant infections are already having a profound impact. In 2019, bacterial AMR was directly responsible for an estimated 1.27 million deaths worldwide - more than HIV/AIDs or malaria.. The actions we take today ... read more

  • Otic Drug Delivery Systems: An Overview

    Humans have five basic senses – sight, touch, hearing, smell and taste and there is a sensory organ associated with each. Thus, hearing is one of vital senses and the ear is a vital sensory organ. read more
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  • Infographic: Seven Softgel Myths

    Softgels are a popular dose format among consumers thanks to their high swallowability and quick onset of action. Yet pharmaceutical developers may not even consider softgels. Why the disconnect? Here are seven popular misconceptions about softgels and the facts that disprove them. read more

  • eBook: Proven Applications Using Variable Pathlength Spectroscopy

    This eBook provides details and insight into using Slope Spectroscopy and the CTech™ SoloVPE® variable pathlength spectroscopy system. The SoloVPE® system provides a rapid, robust, and repeatable, non-disruptive concentration measurement method for proteins, plasmid DNA, and nucleic acid modalities. Articles in this eBook ... read more

  • Analyses of Antibody Drugs Using Inert Ultra High Performance Liquid Chromatography

    This article introduces analyses of monoclonal antibodies (mAbs) and antibody-drug conjugates (ADCs) for quality control using an inert UHPLC system that is extremely resistant to mobile phases containing high salt concentrations. By suppressing the interaction between antibody drugs and stationary phase, the system delivered ... read more

  • Whitepaper: Key Considerations for Extracting Proteins from Recombinant Host Cells

    In the biopharmaceutical industry, quality is pivotal. For a final product to meet quality standards, quality must be built into the production process. Biopharmaceuticals, however, are made from biologically sourced materials, which are inherently variable. read more

  • Whitepaper: How to Develop an Efficient Drug Formulation Process

    Developing an efficient drug formulation development process requires expertise. Ascendia Pharmaceuticals, a leading specialty CDMO, has been recognized as a Partner of Choice by many drug companies because they have solved complex formulations for nearly a decade. Ascendia’s white paper details how to implement a drug discovery... read more
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Webinars

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