{"abstract":"The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled \"How to Obtain a Letter from FDA Stating that Bioequivalence Study Protocols Contain Safety Protections Comparable to Applicable REMS for RLD.\" This draft guidance describes how a prospective abbreviated new drug application (ANDA) applicant may request a letter stating that FDA has determined the following: The potential applicant's bioequivalence (BE) study protocol contains safety protections comparable to those in the risk evaluation and mitigation strategy (REMS) with elements to assure safe use (ETASU) applicable to the reference listed drug (RLD) and FDA will not consider it a violation of the REMS for the RLD sponsor to provide a sufficient quantity of the RLD to the interested generic firm or its agent to allow the firm to perform the testing necessary to support its ANDA.","action":"Notice.","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"body_html_url":"https://www.federalregister.gov/documents/full_text/html/2014/12/05/2014-28540.html","cfr_references":[],"citation":"79 FR 72185","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":"Although you can comment on any guidance at any time (see 21 CFR 10.115(g)(5)), to ensure that the Agency considers your comment on this draft guidance before it begins work on the final version of the guidance, submit either electronic or written comments on the draft guidance by February 3, 2015.","disposition_notes":null,"docket_ids":["Docket No. FDA-2014-D-1891"],"dockets":[],"document_number":"2014-28540","effective_on":null,"end_page":72186,"executive_order_notes":null,"executive_order_number":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2014/12/05/2014-28540.xml","html_url":"https://www.federalregister.gov/documents/2014/12/05/2014-28540/how-to-obtain-a-letter-from-the-food-and-drug-administration-stating-that-bioequivalence-study","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/2014-28540?publication_date=2014-12-05","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2014-12-05/2014-28540/mods.xml","not_received_for_publication":null,"page_length":2,"page_views":{"count":922,"last_updated":"2026-10-25 06:15:04 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2014-12-05/pdf/2014-28540.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2014-28540.pdf?1417700930","publication_date":"2014-12-05","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2014/12/05/2014-28540.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"supporting_documents":[],"comments_url":"https://www.regulations.gov/docketBrowser?rpp=50&so=DESC&sb=postedDate&po=0&dct=PS&D=FDA-2014-D-1891","supporting_documents_count":0,"docket_id":"FDA-2014-D-1891","regulation_id_number":null,"title":"Draft Guidance for Industry on How to Obtain a Letter from FDA Stating that Bioequivalence Study Protocols Contain Safety Protections Comparable to Applicable REMS for RLD; Availability","checked_regulationsdotgov_at":"2020-04-26T03:30:18Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":72185,"subtype":null,"title":"How To Obtain a Letter From the Food and Drug Administration Stating That Bioequivalence Study Protocols Contain Safety Protections Comparable to Applicable Risk Evaluation and Mitigation Strategies for Reference Listed Drugs; Draft Guidance for Industry; Availability","toc_doc":"How to Obtain a Letter from the Food and Drug Administration Stating that Bioequivalence Study Protocols Contain Safety Protections Comparable to Applicable Risk Evaluation, etc.","toc_subject":"Guidance for Industry and Staff:","topics":[],"type":"Notice","volume":79}