Monday, March 31, 2025

March 31, 2025 at 04:30PM Blood Safety & Availability

Blood Safety & Availability

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March 31, 2025 at 02:11PM Indiana Lions Eye Bank, Inc. dba VisionFirst Indiana Lions Eye Bank - 680039 - 06/10/2024

Deviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)

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March 31, 2025 at 01:48PM Transfusion/Donation Fatalities

This page provides details on the Notification Process for Transfusion Related Fatalities and Donation Related Deaths.

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March 31, 2025 at 01:21PM Questions about Tissues

Information about tissues, questions and answers, donor screening and testing, donor eligibility

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Friday, March 28, 2025

March 28, 2025 at 07:50PM Biologics Electronic Reading Room (eFOIA)

The Biologics eFOI Reading Room provides access to documents posted throughout the "Vaccines, Blood & Biologics" and other sections related to the Center for Biologics Evaluation and Research on the FDA.gov Web site.

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March 28, 2025 at 03:59PM Training Course: Achieving Data Quality and Integrity in Maximum Containment Laboratories

To help address challenges associated with ensuring data quality and integrity in regulated studies conducted in BSL-4 laboratories to support MCM development, FDA and UTMB collaborate to provide an annual training course on how to meet GLP requirements in BSL-4 facilities

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March 28, 2025 at 02:29PM Questions about Blood

FDA is responsible for ensuring the safety of the Nation's blood supply. While a blood supply with zero risk of transmitting infectious disease may not be possible, there are several measures taken by FDA to protect and enhance the safety of blood products.

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Monday, March 24, 2025

March 24, 2025 at 08:24PM Ignatius P. Godoy, M.D. - 561662 - 10/01/2018

Bioresearch Monitoring Program/IRB  


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March 24, 2025 at 05:11PM 21st Century LaserMed Pain Institute d/b/a Create Wellness Clinics - 607654 - 07/21/2020

Unapproved and Misbranded Products Related to Coronavirus Disease 2019 (COVID-19)

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March 24, 2025 at 02:23PM HIZENTRA

Product approval information is indicated for treatment of primary immunodeficiency (PI) in adults and pediatric patients 2 years of age and older.

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Friday, March 21, 2025

March 21, 2025 at 06:50PM Recently Issued Guidance Documents

This page lists Recently Issued CBER and Cross-Center Guidance Documents.

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March 21, 2025 at 06:34PM Antimicrobial Resistance

Antimicrobial resistance (AMR)—the ability of a microorganism (bacteria, virus, fungi, parasite) to resist the effects of a drug—is a serious, complex and costly public health problem. Learn what FDA is doing to address AMR.

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Thursday, March 20, 2025

March 20, 2025 at 07:25PM Cleared 510(k) Submissions with Supporting Documents

Listing of cleared 510(k) submissions with supporting documents. Information is reflected as of the clearance date.

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Wednesday, March 19, 2025

March 19, 2025 at 08:52PM Vibrant Health Care, Inc. - 608426 - 11/18/2020

Unapproved and Misbranded Products Related to Coronavirus Disease 2019 (COVID-19)

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March 19, 2025 at 04:45PM Washington Fertility Center - 678931 - 04/30/2024

Deviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)

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Tuesday, March 18, 2025

March 18, 2025 at 07:13PM Kedbumin

Product approval information is indicated for:
o Hypovolemic shock
o Hypoalbuminemia
o Prevention of central volume depletion after paracentesis due to cirrhotic ascites
o Ovarian Hyperstimulation Syndrome (OHSS)
o Adult Respiratory Distress Syndrome (ARDS)
o Burns
o Hemodialysis patients undergoin

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March 18, 2025 at 02:20PM MG Infusions - 696890 - 03/10/2025

CGMP/Deviations/Biologics License Application (BLA)

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March 18, 2025 at 02:12PM CBER Advanced Technologies Team (CATT)

To provide an interactive mechanism within CBER for prospective innovators/developers of advanced manufacturing technologies to discuss the implementation of these technologies in the development of CBER-regulated products.

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Monday, March 17, 2025

March 17, 2025 at 05:04PM Instructions for Using the eBPDR System

For use by biological product manufacturers to report biological product deviations (BPD) that may affect the safety, purity, or potency of a distributed product in accordance with 21 CFR, Part 600.14 or 606.171. Also for use by Human Cells, Tissues and Cellular and Tissue-Based Product (HCT/P) manu

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March 14, 2025 at 04:25PM Fluzone Quadrivalent, Fluzone High-Dose Quadrivalent, Fluzone, Intradermal Quadrivalent, Fluzone Quadrivalent Southern Hemisphere, Fluzone High-Dose Quadrivalent Southern Hemisphere

For active immunization of persons 6 months of age and older for the prevention of influenza disease caused by influenza A subtype viruses and type B viruses contained in the vaccine.

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Thursday, March 13, 2025

March 13, 2025 at 01:18PM CDER Scientific Review Documents Supporting Emergency Use Authorizations for Drug and Biological Therapeutic Products | COVID-19

CDER Scientific Reviews Supporting EUA for Therapeutic Products

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Wednesday, March 12, 2025

March 12, 2025 at 10:39PM ALTUVIIIO

For adults and children with Hemophilia A (congenital Factor VIII deficiency) for: (1) Routine prophylaxis to reduce the frequency of bleeding episodes; (2) On-demand treatment and control of bleeding episodes; and (3) Perioperative management of bleeding.

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March 12, 2025 at 06:39PM CBER 2025 Orphan Approvals (new BLAs)

CBER 2025 Orphan Approvals (new BLAs)

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Tuesday, March 11, 2025

March 11, 2025 at 08:24PM FDA Roundup: March 11, 2025

The U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency.

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March 11, 2025 at 01:14PM Immune Globulin Intravenous (IGIV) and Immune Globulin Subcutaneous (IGSC): Voluntary Lot Withdrawals - Due to Increased Reports of Allergic/Hypersensitivity Reactions

As a precautionary measure, the following lots of Immune Globulin Intravenous (IGIV) and Immune Globulin Subcutaneous (IGSC) have been voluntarily withdrawn by the manufacturers due to a higher rate of allergic/hypersensitivity type reactions, some of which were considered medically significant.

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March 10, 2025 at 08:26PM Section 8400: Marketing Applications

This is the SOPP Section 8400: Marketing Applications main page.

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Friday, March 7, 2025

Thursday, March 6, 2025

March 06, 2025 at 05:20PM Signature Biologics, LLC - 631039 - 02/21/2025

Deviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)

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March 06, 2025 at 05:18PM Signature Biologics, LLC - 631039 - 09/18/2023

Deviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)

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March 04, 2025 at 10:33PM FDA Roundup: March 4, 2025

The U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency.

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