IBM Life Science and business partner InCentric are teaming up to present a seminar on how companies can deal with increasing regulatory requirements in the life sciences and medical device industries.

Speakers at the event will discuss how to:

  • Streamline the development, review, and approval cycles of documentation

  • Access real-time manufacturing documentation and production batch records

  • Shorten time of product deployment through Sales and Marketing

  • Integrate business process management with document management

  • Use innovative technologies that help reduce the time and effort required for validation, implementation, training and migration of systems which address your regulatory issues
  • The seminar will be at the Mariott Durham/RTP in Durham on Feb. 8 starting at 8:30 AM.

    For details, see: www.ibm.com/solutions/LSevents3