federal_register: 2011-31152

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts
2011-31152 Regulatory Site Visit Training Program Notice The Food and Drug Administration's (FDA's) Center for Biologics Evaluation and Research (CBER) is announcing an invitation for participation in its Regulatory Site Visit Training Program (RSVP). This training program is intended to give CBER 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 CBER staff a better understanding of the biologics industry, including its challenges and operations. The purpose of this document is to invite biologics facilities to contact CBER for more information if they are interested in participating in this program. 2011-12-06 2011 12 https://www.federalregister.gov/documents/2011/12/06/2011-31152/regulatory-site-visit-training-program https://www.govinfo.gov/content/pkg/FR-2011-12-06/pdf/2011-31152.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 announcing an invitation for participation in its Regulatory Site Visit Training Program (RSVP). This training program is intended to give CBER regulatory...

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