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January/February 2016

Volume 17, Issue 1

 

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Articles in this Issue

  • Application of LC-MS/MS for the Analysis of Biomolecular Drugs and Biomarkers in Pharmaceutical...

    Nicolas Fourrier
    Mass spectrometry has developed rapidly to become an important analytical technique. However, application to the analysis of biological specimens was at first limited because the ionization processes could only be applied to compounds of low molecular weight, and the instrument interfaces did not permit easy introduction of biological samples into the mass spectrometer.
  • HORIZON LINES: A Quarterly Review of NDAs May-July, 2015

    Sonal Pathak, MS, Harshada Sant, MS, Hemant N. Joshi, Ph.D., MBA
    This column summarizes New Drug Applications (NDAs) from May 2015 to July 2015. In this quarter, FDA approved 26 NDAs.
  • Applying Best Practices from Other Industries to Sponsor-CRO Relationships

    Ashley Hatcher, Jonathan Hughes
    The outsourcing of clinical research is a significant part of the product development landscape in the biopharmaceutical sector. According to analysts, the global clinical research outsourcing (CRO) market was valued at $28.75 billion in 2014 and is forecasted to grow to more than $64 billion by 2020, with nearly 75% of all clinical trials performed by CROs.
  • Technology Transfer Packages for Contract Manufacturing: Iterations During the Development...

    Stuart G. Levy, PhD
    Throughout the developmtent lifecycle of a drug, API manufacturing processes increase in scale and control, as does the level of required process knowledge. Technology transfer packages that reflect the state of knowledge and capability of a given API manufacturing process serve to set the agenda for the next stage of development.
  • The Global Outlook for Generics, Biosimilar and API Manufacturers: Trends, Opportunities &...

    Mike Chace-Ortiz, CEng
    Strong forces continue to shape world pharmaceutical markets, most of which point to continued market share and volume growth for generics. As global R&D spend stays flat, regulations continue to tighten, user fees increase and industry consolidation heats up again, how can manufacturers respond? By analyzing examples of successful industry growth models, what role can information play in helping companies transition to higher value products and services quickly and efficiently? Which sources of information are required to inform these new and different strategies and meet the changing needs of an industry and companies undergoing change?
  • Trends Affecting CROs & CMOs in 2016 Look Positive

    Edward S. Price
    While CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) is getting a lot of attention as this year’s potential wonder therapy, the generics industry continues to undergo change. Positive change.
  • Single-Use Now Key Technology in Biopharmaceutical Manufacturing

    Guy Tiene, MA
    Predictions for healthy growth in demand for biologic drugs are driving many manufacturers, including branded and biosimilar drug producers and contract manufacturers, to invest in new production facilities. These state-of-the-art manufacturing sites often look quite different from traditional plants, however. Rather than massive, three story tall permanent stainless steel reactors, biopharmaceutical companies are opting for much smaller (typically 2000 gallon max) disposable bioreactors. Many factors are influencing this move to single-use technologies, not least are the benefits they provide, such as reduced capital expenditures, reduced risk for cross-contamination, and greater flexibility to meet changing market needs.
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