With rapidly shifting regulatory developments, easy access to regulatory intelligence is crucial to monitor changes in policies and law, and adapt accordingly to ensure compliance in your business’ operations. New technologies and systems need to be implemented by organisations to address the challenges arising from these developments.

Join Generis and fme for this webinar to see how you can access regulatory intelligence in just a single click with the CARA Life Sciences platform. Whether you’re working on a submission or a safety case, CARA Life Sciences provides a database where regulatory intelligence / literature surveillance can be saved; coming in from your own staff or affiliates, or by subscription to services such as Cortellis.

CARA Life Sciences provides more than just a database you can search through, but rather the ability to call up related intelligence wherever you are working. Perhaps you are creating a Variation for an oncology drug for New Zealand; the regulatory intelligence items related to your document’s product, market, therapeutic area and other criteria can be displayed with a single click.

Register to see:

  • The benefits of technology in assisting with literature surveillance for a rapidly changing regulatory landscape
  • A demonstration of CARA Life Sciences’ instant regulatory intelligence capabilities
  • Best practises and tips from fme’s David Gwyn

 

Reserve your spot today!

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