15th Investigator-Initiated Trials Conference

Exl Pharma is excited to bring back the 15th Investigator-Initiated Trials Conference. This is the only conference that offers professionals from pharmaceutical, medical device, and biotechnology companies a complete understanding of the issues and strategies for managing and implementing, successful and compliant, local and global IITs.

ExL Pharma is the proud host of the longest running IIT event and original conference in this field, delivering new educational sessions, never heard before case studies, prominent speakers, loyal attendees (with over 80% from pharmaceutical, medical device, and biotechnology companies), numerous media partners, and tremendous networking opportunities to help build relationships through memorable and relevant shared experiences.

Top Five Reasons To Attend This Conference

  1. This conference teaches the latest strategies for improving IIT implementation and management processes both locally and globally.
  2. Hear directly from leading companies and industry leaders on remaining compliant and adhering to FDA regulations.
  3. Intimate panel discussions uncover the top challenges and solutions to the industry’s most pertinent issues.
  4. Hear and learn from top industry leaders who share "lessons learned" and recent case studies to show how they achieved their desired outcome.
  5. The event is tri-located with the 10th Annual MSL Best Practices Conference and the Medical Affairs Executive Forum which allows for exceptional networking opportunities to discuss best practices and share newly learned information.

Justify Your Trip!

If you have to first convince your boss it’s worth your time and the company’s money to attend this event, you’re not alone. Past conference attendees have helped us create the following justification document that will let you make your case on why this is a must-attend conference for you.

Feel free to download and customize the letter below as you see fit, adding immediate problems you’ll be able to solve and long-term initiatives you’ll be able to implement. Chances are good you’ll be able to do those things and more after the conclusion of our 2012 event!

CLICK HERE TO DOWNLOAD OUR JUSTIFICATION PROPOSAL

Who Should Attend

Professionals from pharmaceutical, biotechnology, and medical device companies with responsibilities in the following departments:

  • Investigator-Initiated Trial
  • Research and Studies
  • Medical Affairs
  • Medical Communications
  • Research Grants
  • Compliance and Regulatory Affairs
  • Contracting and Budgeting
  • Clinical Data Analysis
  • Clinical Affairs
  • Clinical Research
  • External Research / Partnerships
  • Clinical Science
  • Program Management
  • Project Management
  • Study Delivery