Global Regulatory Pre-Workshop
Co-sponsored by the U.S. Food and Drug Administration, the AAADV Global Regulatory Workshop is conducted to learn from senior international regulatory agency personnel from other countries. This unique educational offering is a rare opportunity for investigators, regulatory experts,and drug developers involved in global anti-cancer drug development to interact, in particular those examining populations or sub-populations in which drug development must be conducted internationally.
Pre-Workshop for Patient Advocates
The Pre-Workshop for Patient Advocates is a one-day course held the day before the AAADV Workshop and is intended as an extension of the workshop. It is open to advocates from all disease sites and focuses on how advocates can work more effectively with all stakeholders in the research process to ensure that the patient voice is incorporated across all conversations and decision making.
Open to advocates from all disease sites who are interested in basic training on the role of the U.S. Food and Drug Administration and cancer patient advocates in oncology product development.
Scholarships for patient advocates for the registration fee and support for travel and housing are available. Please click HERE for a Patient Advocate scholarship application.