Patient Advocacy Group Pass | Orphan USA

Patient Advocacy Group Pass | Orphan USA



INTERNATIONAL

World Orphan Drug Congress USA 2019, 10-12 April, USA

Are you a patient advocacy group interested in attending World Orphan Drug Congress USA 2019?

 

We are offering a limited number of complimentary VIP passes to patient groups.   To apply for a Patient Advocacy pass, please emailAnna.Bagley@terrapinn.com .  

 

This complimentary VIP pass to the three-day event will allow you to:

• Full access to all conference activities on April 10th, 11th and 12th. 
• Make global connections with other patient groups, regulators, payers and pharma/biotech stakeholders that can help support your mission and further position your organization
• Strengthen your bonds with industry stakeholders and achieve collaborations that can help accelerate the path to treatments
• Hear about the FDA’s and industry’s patient focused drug development initiatives and partnerships and how you can benefit from them
• Network, engage, learn and keep contributing to a multi-stakeholder effort to accelerate orphan drug development; as well as schedule 1-on-1 meetings with any attendee of the congress by using the event networking system

Click here to see the Rare Disease Advocacy agenda >

 

VIP invitation covers your registration fee ($2,000 waived) and you are responsible from your own travel and hotel arrangements. 

To apply for a Patient Advocacy pass, please email Anna.Bagley@terrapinn.com   

 

Please note, only 100 guest passes are given annually to patient advocacy groups to attend the conference so make sure to reserve your pass now!