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Navigate Global Regulations and Improve RBM Processes to Enhance Data Quality and Trial Efficiency

September 14-15, 2017
  • Barcelona, Spain

Who Should Attend

You will benefit from attending this event if you are an executive, senior level director or manager from the pharmaceutical, biotech or CRO industries with responsibilities or involvement in the following areas:

  • Clinical Operations
  • Study Monitoring
  • Clinical Research
  • Data Management
  • Clinical Quality
  • Clinical Compliance
  • Quality Assurance
  • Study Management
  • Regulatory Affairs
  • Statistics

This conference will also benefit clinical monitoring and data management service vendors as well as clinical and quality risk consultants.

A Great Place to Meet Your Market!

Take advantage of the best opportunity to meet potential clients face-to-face.
Build relationships while demonstrating thought leadership and sharing expertise.
For more information on how to position your company as a sponsor or exhibitor, contact
Steven Sica at 339-298-2281 or email [email protected].

You will benefit from attending this event if you are an executive, senior level director or manager from the pharmaceutical, biotech or CRO industries with responsibilities or involvement in the following areas:

  • Clinical Operations
  • Study Monitoring
  • Clinical Research
  • Data Management
  • Clinical Quality
  • Clinical Compliance
  • Quality Assurance
  • Study Management
  • Regulatory Affairs
  • Statistics

This conference will also benefit clinical monitoring and data management service vendors as well as clinical and quality risk consultants.

A Great Place to Meet Your Market!

Take advantage of the best opportunity to meet potential clients face-to-face.
Build relationships while demonstrating thought leadership and sharing expertise.
For more information on how to position your company as a sponsor or exhibitor, contact
Steven Sica at 339-298-2281 or email [email protected].