Code of Federal Regulations · Subpart

Subpart P — Variances

21 C.F.R. pt. 112, subpt. P

• § 112.171 Who May Request A Variance From The Requirements Of This Part?
• § 112.172 How May A State, Tribe, Or Foreign Country Request A Variance From One Or More Requirements Of This Part?
• § 112.173 What Must Be Included In The Statement Of Grounds In A Petition Requesting A Variance?
• § 112.174 What Information Submitted In A Petition Requesting A Variance Or Submitted In Comments On Such A Petition Are Publicly Available?
• § 112.175 Who Responds To A Petition Requesting A Variance?
• § 112.176 What Process Applies To A Petition Requesting A Variance?
• § 112.177 Can An Approved Variance Apply To Any Person Other Than Those Identified In The Petition Requesting That Variance?
• § 112.178 Under What Circumstances May Fda Deny A Petition Requesting A Variance?
• § 112.179 When Does A Variance Approved By Fda Become Effective?
• § 112.180 Under What Circumstances May Fda Modify Or Revoke An Approved Variance?
• § 112.181 What Procedures Apply If Fda Determines That An Approved Variance Should Be Modified Or Revoked?
• § 112.182 What Are The Permissible Types Of Variances That May Be Granted?