viernes, 17 de julio de 2020

What’s New for Biologics | FDA

What’s New for Biologics | FDA





7/16/2020Considerations for the Use of Real-World Evidence to Assess the Effectiveness of Preventive Vaccines
7/14/2020Diagnosis and Pathogenesis of Hepatitis Viruses That Impact the Safety of Blood and Related Products
7/13/2020Understanding the Interplay Between Host Immunity and Viral Factors for Rational Design of Vaccines Against Vector-Borne Viral Pathogens
7/10/2020Study of antibody response to SARS-CoV-2 spike proteins could help inform vaccine design
7/10/2020July 9, 2020 Approval Letter - FluMist
7/9/2020Regenerative Medicine Advanced Therapy Designation
7/7/2020Summary of Safety and Effectiveness  - Alinity m HIV-1
7/6/2020July 2, 2020 Approval Order - Alinity m HIV-1
7/6/2020July 2, 2020 Approval Letter - Flucelvax
7/6/2020July 2, 2020 Approval Letter - Fluad and Fluad Quadrivalent
7/6/2020July 2, 2020 Approval Letter - FluLaval
7/2/2020July 2, 2020 Approval Letter - Afluria
7/2/2020July 2, 2020 Approval Letter - Fluarix Quadrivalent
7/2/2020July 2, 2020 Approval Letter - Flublok
7/2/2020July 2, 2020 Approval Letter - Fluzone Quadrivalent and Fluzone High-Dose Quadrivalent
7/2/2020Influenza Vaccine for the 2020-2021 Season
7/2/2020Updated Information for Human Cell, Tissue, or Cellular or Tissue-based Product (HCT/P) Establishments Regarding the COVID-19 Pandemic
7/2/2020Complete List of Licensed Products and Establishments
7/2/2020Complete List of Substantially Equivalent 510(k) Device Applications
7/2/2020Complete List of Currently Approved Premarket Approvals (PMAs)
7/2/2020Complete List of Currently Approved NDA and ANDA Application Submissions
7/2/2020Testing Human Cells, Tissues, and Cellular and Tissue Based Product (HCT/P) Donors for Relevant Communicable Disease Agents and Diseases
7/1/2020Expiration Date Extension for MicRhoGAM (Rho(D) Immune Globulin) Lot MVP116A1 through July 19, 2021
6/30/2020Evaluation of Therapeutic Approaches Based on Genome Editing and Stem Cell Technologies
6/30/2020Development and Licensure of Vaccines to Prevent COVID-19; Guidance for Industry
6/29/2020Exceptions and Alternative Procedures Approved Under 21 CFR 640.120
6/26/2020June 26, 2020 Approval Letter - BeneFIX
6/25/2020Summary Basis for Regulatory Action - Blood Grouping Reagent, Anti-Lea, Anti-Leb
6/24/2020Guidance Agenda: Guidance Documents CBER is Planning to Publish During Calendar Year 2020
6/24/2020June 9, 2020 Clinical Review - GARDASIL 9
6/19/2020June 19, 2020 Approval Letter - Measles, Mumps, and Rubella Virus Vaccine Live
6/19/2020June 18, 2020 Approval Letter - Blood Grouping Reagent, Anti-Lea (Murine Monoclonal)(For Further Manufacturing Use)
6/19/2020June 18, 2020 Approval Letter - Blood Grouping Reagent, Anti-Leb (Murine Monoclonal)(For Further Manufacturing Use)
6/19/2020BK190356 - PrepaCyte-CB Processing System
6/18/2020eSubmitter Application History

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