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LitTrace

Literature Monitoring Tool

LitTrace is a customizable literature monitoring and tracking tool that ensures timely access to reliable and consolidated information on relevant safety-related literature and creates databases for ICSR's and similar compliance reports.

LitTrace can be used to monitor literature relating to:

  • Clinical evaluation
  • Pre-market approval
  • Adverse events reporting

Benefits of LitTrace include:

  • Fully customizable – per client's unique requirements
  • Flexible folder structure – build multiple folders based on product or therapeutics areas (including subfolders)
  • Import third party data – EMBASE, MEDLINE, etc.
  • Simple, easy-to-use tool – for assessment workflow tracking
  • Configurable reporting engine
  • Flexible delivery options – client environment or Bioclinica hosted
  • Central repository – for weekly hits and full-text articles
  • One-stop solution to track full-text article – translation and contract author requests preparation and compliance as required by the FDA, EMEA and other global regulatory bodies

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ADDITIONAL RESOURCES

LitTrace and PVTrace

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Meet the Bioclinica Safety and Regulatory Team: Sukrit Singh, Engagement Manager

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Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely.

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