SBIA Education Events

Supporting Events from FDA CDER Small Business & Industry Assistance

Global Access to Medicines 2022 Banner

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

Agenda & Speaker Bios

PDF Download
Event Agenda

The agenda may be updated as it is refined. The current version of the agenda is v7, updated on August 13, 2022.

PDF Download
Speaker Biographies

The speaker biographies document is currently being finalized and will be pasted here when it is ready.

LOGIN Information

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:

Files, Certificate, & Recordings

Download Presentation Slides:

The links above will become active on the day before the workshop.

Evaluation & Certificate:

Evaluation & Certificate of Attendance

Session Recordings:

Questions & More Information

Continuing Education:

    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:

  • 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.


Please refer the FAQs page on this website. If you are not able to find your answer there, please email us at

More Information

If you have questions regarding the content of the event or other CDER-specific information, please: