IRB Documents

The Cimzia® Safety Registry is a part of the overall NDB Study and listed below are the documents you may need for IRB submission.

Click here to request any of the documents above.

Because this study does not involve any treatment and patients cannot be identified in any manner, you should be able to utilize your IRB expedited review process.

If you require IRB approval to participate in this study, please contact your IRB as soon as possible.

If you have any questions, or need assistance, please contact: Rebecca Schumacher, at: 316-263-2125 x119