federal_register: E6-5221

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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
E6-5221 Regulatory Site Visit Training Program Notice The Food and Drug Administration's (FDA's) Center for Biologics Evaluation and Research (CBER) is reannouncing the invitation for participation in its Regulatory Site Visit Training Program (RSVP). This training program is intended to give CBER's regulatory review, compliance, and other relevant staff an opportunity to visit biologics facilities. These visits are intended to allow CBER staff to directly observe routine manufacturing practices and to give staff a better understanding of the biologics industry, including its challenges and operations. This notice invites biologics facilities interested in participating in this program to contact CBER for more information. 2006-04-11 2006 4 https://www.federalregister.gov/documents/2006/04/11/E6-5221/regulatory-site-visit-training-program https://www.govinfo.gov/content/pkg/FR-2006-04-11/pdf/E6-5221.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration's (FDA's) Center for Biologics Evaluation and Research (CBER) is reannouncing the invitation for participation in its Regulatory Site Visit Training Program (RSVP). This training program is intended to give CBER's...  

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