federal_register: E9-919

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts regulation_id_numbers
E9-919 Draft Guidance for Industry: Current Good Tissue Practice (CGTP) and Additional Requirements for Manufacturers of Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps); Availability Notice The Food and Drug Administration (FDA) is announcing the availability of a draft document entitled "Guidance for Industry: Current Good Tissue Practice (CGTP) and Additional Requirements for Manufacturers of Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT[sol]Ps)" dated January 2009. The draft guidance document provides establishments that manufacture HCT[sol]Ps with recommendations for complying with CGTP requirements. 2009-01-16 2009 1 https://www.federalregister.gov/documents/2009/01/16/E9-919/draft-guidance-for-industry-current-good-tissue-practice-cgtp-and-additional-requirements-for https://www.govinfo.gov/content/pkg/FR-2009-01-16/pdf/E9-919.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 document entitled "Guidance for Industry: Current Good Tissue Practice (CGTP) and Additional Requirements for Manufacturers of Human Cells, Tissues, and Cellular and...  

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