Articles in this Issue

  • CMC Development Strategies for Small Pharma

    James Bernstein Ph.D.
    A significant trend in the pharmaceutical industry is the increasing proportion of early drug development carried out in smaller organizations, as opposed to the large vertically-integrated pharmaceutical companies. Most of these small organizations use contract development and manufacturing organizations (CDMO’s) for the Chemistry, Manufacturing and Controls (CMC) aspects of development. In this model of drug development, a small innovator organization works in partnership with contract organizations for the early non-clinical, clinical, and CMC aspects of drug development.
  • How a Training Strategy Can Improve Clinical Trial Performance

    Laura Brown, Ph.D.
    Pharmaceutical companies are facing the increasingly-stressful challenge of delivering greater performance at less cost and in less time while complying with a rising number of regulations and guidelines (such as ICH GCP and the Clinical Trial Directive). This places tremendous pressure on the technical and managerial skill base of all companies, large, medium or small.
  • Insights Gained into the Identification, Qualification and Utilization of CRO Laboratories...

    Dennis Jenke, Ph.D.
    During their manufacture, storage and use, pharmaceutical drug products come into contact with polymeric materials, components and systems. Although these components and systems are constructed from materials and by processes that seek to minimize the extent to which contact can occur, neither truly inert materials and systems nor truly benign contact conditions exist and interactions which potentially impact product quality can occur. One such interaction is the migration of components out of the material and into the pharmaceutical drug product. Migrating substances are a concern due to their potential impact on the finished drug product’s suitability for use. For example, migratory substances could adversely affect the safety and efficacy of the finished drug product, directly or indirectly. The extent of migration must be evaluated, and it must be established that the impact of the migration is within acceptable values.
  • Cold Chain Roundtable

    Matty Toomb, C. Ray Goff, Jr., Kevin Michael Lawler, Martin Peter, Melissa Germain, M.Sc., Jean-Pierre Emond, Ph.D., Jamie Chasteen, Kenneth Lukes, Henry Ames
    MT: It seems that when American Thermal Instruments introduced our cloud-based temperature management system two years ago, we were the only company that had a flat screen in our tradeshow booth talking about transmitting data and apps. Now, it does not matter what the product line is, every supplier is talking about their cloud and the need to hire software engineers and suppliers to their workforce.
  • Avoiding Pitfalls during Technology Transfer of Cell Culture Manufacturing Processes in the...

    Michael Pohlscheidt, Mahalia Corrales, Salim Charanyia, Eric Fallon, Manfred Bruch, Marco Jenzsch, Christian Sieblist
    Since the early 1980s, biotechnology products have shaped the pharmaceutical industry. A large number of monoclonal antibodies and therapeutic proteins have been approved and are predicted to be the major source of revenue in upcoming years for the industry
  • <<
  • >>