This PDF is the current document as it appeared on Public Inspection on 04/01/2014 at 08:45 am.
Food and Drug Administration, HHS.
Notice of public workshop; request for comments.
The Food and Drug Administration (FDA) is announcing a public workshop entitled “Standards for the Interoperable Exchange of Information for Tracing of Human, Finished, Prescription Drugs, in Paper or Electronic Format.” This public workshop will provide a forum for discussing the development of these standards in the Drug Supply Chain Security Act of 2013. In particular, participants will be asked to provide information, current practices, research, and ideas on the interoperable exchange of transaction information, transaction history, and transaction statements, in paper or electronic format, for each transfer of drug product in which a change of ownership occurs. This public workshop will also provide a forum to discuss the feasibility of establishing standardized documentation to be used by members of the pharmaceutical distribution supply chain to convey this information to the subsequent purchaser of a drug product and to facilitate the exchange of lot level data. As FDA continues to work on developing standards for interoperable exchange, the Agency is seeking public input to ensure that we consider information regarding all drug supply chain stakeholders.
The public workshop will be held on May 8 and 9, 2014, from 9 a.m. to 5 p.m.
The public workshop will be held at FDA's White Oak Campus, 10903 New Hampshire Ave. Bldg. 31 Conference Center, the Great Room (rm. 1503A), Silver Spring, MD 20993. Entrance for the public meeting Start Printed Page 18563participants (non-FDA employees) is through Building 1 where routine security check procedures will be performed. For parking and security information, please refer to http://www.fda.gov/AboutFDA/WorkingatFDA/BuildingsandFacilities/WhiteOakCampusInformation/ucm241740.htm.Start Further Info
FOR FURTHER INFORMATION CONTACT:
Connie T. Jung, Office of Compliance, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993, 301-796-3130, FAX: 301-847-8722, email: email@example.com.
Comments: In order to permit the widest possible opportunity to obtain public comment, FDA is soliciting either electronic or written comments on all aspects of the public workshop topics. The deadline for submitting comments related to this public workshop is June 9, 2014.
Regardless of attendance at the public workshop, interested persons may submit either electronic comments regarding the topics of the workshop to http://www.regulations.gov or written comments to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. It is only necessary to send one set of comments. Identify comments 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, and will be posted to the docket at http://www.regulations.gov.
Registration: To register for the workshop either: (1) Email your registration information to firstname.lastname@example.org or (2) mail your registration information to Connie T. Jung (see Contact Person). Registration information should include:
- “Registration” in the subject line, and
- Registrant name, company or organization, address, phone number, and email address in the body of your email or mailing.
Registration requests should be received by April 24, 2014. Registration is free. Seats are limited. FDA may limit the numbers of participants from each organization based on space limitations. Registrants will receive confirmation upon acceptance for participation in the workshop. Onsite registration on the day of the meeting will be based on space availability on the day of the event starting at 8 a.m. If registration reaches maximum capacity, FDA will post a notice closing meeting registration for the workshop on FDA's Web site at: http://www.fda.gov/Drugs/NewsEvents/ucm388993.htm.
If you need special accommodations due to a disability, please contact Connie Jung (see FOR FURTHER INFORMATION CONTACT) at least 7 days in advance of the public workshop.End Further Info End Preamble Start Supplemental Information
On November 27, 2013, the Drug Supply Chain Security Act (DSCSA) (Title II, Pub. L. 113-54) was signed into law. The DSCSA outlines critical steps to build an electronic, interoperable system over the next 10 years to identify and trace certain prescription drugs as they are distributed within the United States. Section 202 of the DSCSA, which adds section 582(a)(2)(A) to the Federal Food, Drug, and Cosmetic Act (the FD&C Act), requires the Secretary to establish initial standards for the interoperable exchange of transaction information, transaction history, and transaction statements, in paper or electronic format, in consultation with other appropriate Federal officials, manufacturers, repackagers, wholesale drug distributors, dispensers, and other pharmaceutical distribution supply chain stakeholders. The system that will be established under the DSCSA will enhance FDA's ability to help protect U.S. consumers from exposure to drugs that may be counterfeit, stolen, contaminated, or otherwise harmful by improving detection and removal of potentially dangerous drugs from the drug supply chain.
FDA has used a multilayered approach to improve the security of the drug supply chain to protect U.S. patients from unsafe, ineffective, and poor quality drugs. In addition to considering the standards developed under section 505D of the FD&C Act (21 U.S.C. 355e), the DSCSA directs FDA to establish initial standards for trading partners to utilize to achieve the interoperable exchange of transaction information, transaction history, and transaction statements. On February 20, 2014, FDA issued a Federal Register notice (79 FR 9745) that established a public docket (Docket No. FDA-2014-N-0200) for this topic. FDA is seeking additional stakeholder input based on the information received in that docket.
II. Purpose of the Workshop
This public workshop is intended to provide an opportunity for interested persons to share information, current practices, research, and ideas on the feasibility of establishing standardized documentation to be used by members of the pharmaceutical distribution supply chain to convey the transaction information, transaction history, and transaction statement to the subsequent purchaser of a drug product and to facilitate the exchange of lot level data. In addition, FDA is interested in learning about practices, processes, and systems that supply chain stakeholders currently use to exchange information, such as product information, information related to the sale or change of ownership of prescription drugs, or communications about drugs in distribution. Discussions at this public workshop may also include current practices and suggestions for the exchange of information between supply chain stakeholders to provide, receive, and terminate notifications. Discussions may also include how trading partners should respond to requests for verification of suspect drug product, and respond to requests for information from FDA or other appropriate Federal or State officials in the event of a recall or for the purpose of investigating a suspect or illegitimate drug product. Participants will not be asked to develop consensus opinions during the discussion, but rather to provide their individual perspectives. By May 2, 2014, FDA will post the following information on our Web site under Standards Development for Interoperable Exchange of Tracing Information at http://www.fda.gov/Drugs/NewsEvents/ucm388993.htm:
- Workshop agenda;
- Workshop discussion topics.
Dated: March 27, 2014.
Assistant Commissioner for Policy.
[FR Doc. 2014-07335 Filed 4-1-14; 8:45 am]
BILLING CODE 4160-01-P