federal_register: 2010-30387

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts
2010-30387 Draft Guidance for Industry on Residual Solvents in Animal Drug Products; Questions and Answers; Availability Notice The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry <greek-i>211 entitled "Residual Solvents in Animal Drug Products; Questions and Answers." The draft questions and answers (Q&A) guidance addresses the United States Pharmacopeia (USP) General Chapter <467> Residual Solvents that applies to both human and veterinary drugs and to compendial and non- compendial drug products. This document answers questions regarding CVM's implementation of USP <467> Residual Solvents. 2010-12-03 2010 12 https://www.federalregister.gov/documents/2010/12/03/2010-30387/draft-guidance-for-industry-on-residual-solvents-in-animal-drug-products-questions-and-answers https://www.govinfo.gov/content/pkg/FR-2010-12-03/pdf/2010-30387.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry <greek-i>211 entitled "Residual Solvents in Animal Drug Products; Questions and Answers." The draft questions and answers (Q&A) guidance addresses...

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