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The practice of pre-marketing safety assessment in drug development.

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Journal of biopharmaceutical statistics

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      Abstract

      The last 15 years have seen a substantial increase in efforts devoted to safety assessment by statisticians in the pharmaceutical industry. While some of these efforts were driven by regulations and public demand for safer products, much of the motivation came from the realization that there is a strong need for a systematic approach to safety planning, evaluation, and reporting at the program level throughout the drug development life cycle. An efficient process can help us identify safety signals early and afford us the opportunity to develop effective risk minimization plan early in the development cycle. This awareness has led many pharmaceutical sponsors to set up internal systems and structures to effectively conduct safety assessment at all levels (patient, study, and program). In addition to process, tools have emerged that are designed to enhance data review and pattern recognition. In this paper, we describe advancements in the practice of safety assessment during the premarketing phase of drug development. In particular, we share examples of safety assessment practice at our respective companies, some of which are based on recommendations from industry-initiated working groups on best practice in recent years.

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      Author and article information

      Affiliations
      [1 ] Statistical Research and Consulting Center, Pfizer Inc, Kalamazoo, Michigan 49009, USA. christy.j.chuang-stein@pfizer.com
      Journal
      J Biopharm Stat
      Journal of biopharmaceutical statistics
      1520-5711
      1054-3406
      2013
      : 23
      : 1
      23331218
      10.1080/10543406.2013.736805

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