Advancing Generic Drug Development Workshop:
Translating Science to Approval
September 20-21, 2022
The agenda is still being refined and may be updated over time. The current version is v4, uploaded on August 13, 2022.
The speaker biographies document is under development and will be linked here when it is ready.
The virtual conference will be hosted via Adobe Connect and is limited to 2,000 simultaneous attendees (1,000 each in Room One and Room Two). If a room is full when you attempt to enter, please try the other room.
The links below to the Adobe Connect rooms will be activated shortly before the event begins.
Please select the correct room based on the first letter of your LAST NAME.
Select the first room if you require closed captioning.
The above rooms will open ~15 minutes before each day begins.
If you encounter any technical issues, visit the Technical Issues Support Page
The audio for the event will be provided through your computer speakers via Adobe Connect (there will NOT be a teleconference number to dial into). We recommend that you test your PC or mobile device prior to the event and you join the event a few minutes early to address any issues.
To test your PC, please visit:
Download Presentation Slides:
The links above will become active on the day before the workshop.
Evaluation & Certificate:
Evaluation & Certificate of Attendance
The above link will become active near the close of the second day of the Workshop.
The recordings of the Forum sessions will be linked here as soon as they are available.
- pre-approved by RAPS as eligible for a maximum of 12 credits for a two day event (appropriate to real-time attendance) towards a participant’s RAC recertification upon full completion.
- pre-approved by SOCRA who accepts documentation of candidate participation in continuing education programs for re-certification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area.
- pre-approved by SQA as eligible for 1 non-GCP or non-GLP unit for every 1 hour of instructional time towards a participant’s RQAP re-registration.
- approved by ACRP for continuing education in clinical research. ACRP will provide 1 ACRP contact hour for every 45-60 minutes of qualified material.
Real-time attendance is required for the certificate of attendance which can be used in support of CEs for the following professional organizations. Certificates are only available during the two weeks post-event (until October 5, 2022).
This workshop has been:
If you have questions regarding the content of the event or other CDER-specific information, please: