2nd Interim Analysis Symposium -

2nd Interim Analysis Symposium
March 26 - 27, 2018
Philadelphia, PA

The 2nd Interim Analysis Symposium will provide drug safety and clinical operations teams with best practices and tried-and-true strategies that will enhance the capacity at which organizations can produce upstanding reports about the results of their ongoing studies and expedite effective products to market.

2nd Interim Analysis Symposium – 2nd Interim Analysis Symposium

Announcements regarding the safety and efficacy results of ongoing studies are of great interest to the stakeholders of your organization and it is essential that the counterparts of your clinical research teams collaborate to effectively disseminate this sensitive material.
The 2nd Interim Analysis Symposium will provide drug safety and clinical operations teams with best practices and tried-and-true strategies that will enhance the capacity at which organizations can produce upstanding reports about the results of their ongoing studies and expedite effective products to market.

Don’t miss out on this opportunity to consult with and learn from industry experts during interactive panel discussions, advanced case studies, engaged roundtables and peer networking breaks.

Top Five Reasons to Attend

  1. Analyze real-world examples of interim analysis and adaptive design evolution
  2. Consider trial designs that maximize efficiency and allow for quicker FDA submissions
  3. Maintain confidentiality of interim data to enhance trial integrity and credibility
  4. Improve the collaboration between the counterparts of your clinical research teams
  5. Consult with industry experts for guidance on operative procedures that expedite trial timelines and effective products to market

Who Should Attend

This conference is designed for professionals from pharmaceutical companies with responsibilities in the following areas:

  • Drug Safety
  • Clinical Operations/ Research/ Management
  •  Statistics
  • Biostatistics & Epidemiology
  • Trial Design & Development
  •  Clinical/ Medical Informatics
  •  Adaptive Clinical Trials
  •  Global Regulatory Policy
  • Quantitative & Scientific Affairs
  • Data Analysis
  • Medical Coding
  • Regulatory Affairs & Compliance
  • Medical Research
  • Product Development
  • Compound Development

This event is also of interest to:

  • Data Monitoring Committee Providers
  • Data Coordinating Centers
  • Contract Research Organizations
  • Electronic Data Capture Vendors
  • Medical Informatics/ Data Service Providers
  • Statistical Consultants
  • Pharmacokinetic Vendors
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