CDER SBIA and FDA’s Center for Devices and Radiological Health (CDRH) are pleased to announce another 2-day Regulatory Education for Industry (RedI) Conference!
Because the regulatory principles of drugs and devices are both similar and different, the REdI Conference features a cross-cutting plenary addressing issues which impact both drugs and devices, as well as individual break-out sessions which focus on the unique issues and regulatory requirements of drugs and devices.
* Register Now *
This LIVE event is FREE and will be webcast and recorded. You may attend either “In-Person Onsite” or “Virtually via Adobe Connect.”
Pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
NETWORKING opportunities available
PLENARY: FDA Insights on Products for Rare Diseases and Pediatrics
Topics include: Manufacturing Process Validation; Interactions with FDA; Emerging Technology and Inspection of NDA and BLA applications…
Note: Venue is accessible to persons with disabilities. If you have any special accommodation needs, please make requests as soon as possible to info@SBIAevents.com
**NOTE: We have a block of rooms at a discounted rate, that will be available on a first-come, first-served basis until September 12, 2016, or until the block is filled.
Questions: For conference registration questions or logistical questions, contact: info@SBIAevents.com
For more information:
CDER SBIA
.png)
No hay comentarios:
Publicar un comentario