The following list contains drafts of proposed guidance documents. In an effort to get fair and balanced input from the veterinary biologics industry prior to finalizing guidance documents, the CVB posts selected draft guidance documents for a 3-week comment period. See CVB Notice 05-16.
If you wish to have your comments on any of the draft documents listed below considered by the CVB, use the following procedure:
1) Submit comments by e-mail addressed to email@example.com.
2) Format the subject line of the e-mail to read "Comments on draft notice/memo <insert ID number>"
3) Submit comments by 12:00 PM (central time) on the due date indicated for each document.
4) The CVB will acknowledge receipt of the comments by return e-mail. Responses to e-mail content will not be provided.
VS 800 series Memoranda and CVB Notices - Historical Summary of Proposed Documents (May 31, 2016 - 92 KB)
|Veterinary Services Memoranda|
|General Licensing Considerations: Field Safety Studies||DRAFT 546||February 27, 2017|
|Guidelines for the Preparation and Review of Labeling Materials *posted for a second round of comments||DRAFT 579||March 6, 2017|
|Autologous Therapeutic Biologics||DRAFT 567||March 13, 2017|
|Electronic Record Keeping and Compliance with 9 CFR Part 116 *posted for a second round of comments||DRAFT 576||March 13, 2017|