Regulatory Best Practices for Global Access to Medicines,
Including Anti-TB Medicines Conference
August 16 – 18, 2022
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Register Once for All Three Days
The agenda may be updated as it is refined. The current version of the agenda is v7, updated on August 13, 2022. |
The speaker biographies document is currently being finalized and will be pasted 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.
Last Name A – I(or if you require closed captions) |
NOTE: Viewing the Livestream does NOT allow you to submit questions.
You should attend in Adobe Connect if you wish to submit questions.
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:
https://concerted.adobeconnect.com/common/help/en/support/meeting_test.htm
Download Presentation Slides:
The links above will become active on the day before the workshop.
Evaluation & Certificate:
Evaluation & Certificate of Attendance
Session Recordings:
- Day One YouTube Livestream Recording
- Day Two YouTube Livestream Recording (coming soon)
- Day Two YouTube Livestream Recording (coming soon)
Continuing Education:
- 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 September 1, 2022).
This workshop has been:
Questions?
Please refer the FAQs page on this website. If you are not able to find your answer there, please email us at info@sbiaevents.com.
More Information
If you have questions regarding the content of the event or other CDER-specific information, please:
- Visit the CDER SBIA website
- Learn more about CDER SBIA Workshops and Webinars
- Subscribe to the CDER SBIA email updates
- Follow us on LinkedIn