Current Good Manufacturing Practice Requirements for Combination Products; Extension of Comment Period

Federal Register: November 10, 2009 (Volume 74, Number 216)

Proposed Rules

Page 57973-57974

From the Federal Register Online via GPO Access [wais.access.gpo.gov]

DOCID:fr10no09-24

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration 21 CFR Part 4

Docket No. FDA-2009-N-0435

Current Good Manufacturing Practice Requirements for Combination

Products; Extension of Comment Period

AGENCY: Food and Drug Administration, HHS.

ACTION: Proposed rule; extension of comment period.

SUMMARY: The Food and Drug Administration (FDA) is extending to

February 5, 2010, the comment period for the proposed rule that appeared in the Federal Register of September 23, 2009. In the proposed rule, FDA requested comments on current good manufacturing practice

(CGMP) requirements applicable to combination products. The agency is taking this action in response to requests for an extension to allow interested persons additional time to submit comments.

DATES: The comment period for the proposed rule publishied September 23, 2009 (74 FR 48423), is extended. Submit electronic or written comments by February 5, 2010.

ADDRESSES: You may submit comments, identified by Docket No. FDA-2009-

N-0435, by any of the following methods:

Electronic Submissions

Submit electronic comments in the following way:

Federal eRulemaking Portal: http://www.regulations.gov.

Follow the instructions for submitting comments.

Written Submissions

Submit written submissions in the following ways:

FAX: 301-827-6870.

Mail/Hand delivery/Courier (for paper, disk, or CD-ROM submissions): Division of Dockets Management (HFA-305), Food and Drug

Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.

To ensure more timely processing of comments, FDA is no longer accepting comments submitted to the agency by e-mail. FDA encourages you to continue to submit electronic comments by using the Federal eRulemaking Portal, as described previously, in the ADDRESSES portion of this document under Electronic Submissions.

Instructions: All submissions received must include the agency name and docket number for this rulemaking. All comments received may be posted without change to http://www.regulations.gov, including any personal information provided. For additional information on submitting comments, see the ``Comments'' heading of the SUPPLEMENTARY INFORMATION section of this document.

Docket: For access to the docket to read background documents or comments received, go to http://www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ``Search'' box and follow the prompts and/or go to the Division of

Dockets Management, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.

FOR FURTHER INFORMATION CONTACT: John Barlow Weiner, Office of

Combination Products (HFG-3), Food and Drug Administration, 15800

Crabbs Branch Way, Suite 200, Rockville, MD 20855 301-427-1934.

SUPPLEMENTARY INFORMATION:

1. Background

   In the Federal Register of September 23, 2009 (74 FR 48423), FDA published a proposed rule with a 90-day comment period to request comments on CGMP requirements applicable to combination products.

   Comments on the proposed rule will inform FDA's rulemaking to establish regulations for current good manufacturing practices for combination products.

   Page 57974

   The agency has received requests for a 45-day extension of the comment period for the proposed rule. Each request conveyed concern that the current 90-day comment period does not allow sufficient time to develop a meaningful or thoughtful response to the proposed rule.

   FDA has considered the requests and is extending the comment period for the proposed rule for 45 days, until February 5, 2010. The agency believes that a 45-day extension allows adequate time for interested persons to submit comments without significantly delaying rulemaking on these important issues.

2. Request for Comments

   Interested persons may submit to the Division of Dockets Management

   (see ADDRESSES) electronic or written comments on this document. Submit a single copy of electronic comments or two paper copies of any mailed comments, except that individuals may submit one paper copy. Comments are to be identified with the docket number found in brackets in the heading of this document. Received comments may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.

   Dated: November 4, 2009.

   David Horowitz,

   Assistant Commissioner for Policy.

   FR Doc. E9-26966 Filed 11-9-09; 8:45 am

   BILLING CODE 4160-01-S