Friday, January 31, 2025

February 01, 2025 at 12:53AM Data Standards for Drug and Biological Product Submissions Containing Real-World Data

Data Standards for Drug and Biological Product Submissions Containing Real-World Data

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February 01, 2025 at 12:32AM Patient Engagement Collaborative

The Patient Engagement Collaborative (PEC) is an advancement in the FDA’s efforts to strengthen its relationship with patient communities and is being coordinated by the FDA’s Public Engagement Staff.

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January 31, 2025 at 10:16PM Human Gene Therapy for Hemophilia

Human Gene Therapy for Hemophilia, Draft Guidance for Industry, CBER, biologics

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January 31, 2025 at 06:32PM It’s a Good Time to Get Your Flu Vaccine

Getting vaccinated in the fall can lower your chances of getting the flu. Haven’t had your flu shot yet? It’s not too late. Every flu season is different. Your best defense against the flu is to get a vaccine every year.

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January 31, 2025 at 04:05PM SPIKEVAX

COVID19 Vaccine, mRNA

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January 31, 2025 at 03:01PM Evaluation of Sex Differences in Clinical Investigations

Evaluation of Sex Differences in Clinical Investigations - IRB Information Sheet

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Thursday, January 30, 2025

January 30, 2025 at 10:08PM Patient Listening Session Summaries

Patient Listening Session summaries are published after each session to share a high-level summary of the discussion. The Public Engagement Staff draft summaries for FDA-requested sessions and the patient community requester drafts summaries for Patient-led sessions.

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January 30, 2025 at 08:37PM Clinical Review - Fluarix

•For active immunization of persons 3 years of age and older for the prevention of disease caused by influenza virus subtypes A and type B contained in the vaccine.

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January 30, 2025 at 08:11PM Final Statistical Review and Evaluation - Novoeight

Product approval information is indicated for control and prevention of bleeding episodes in adults, adolescents and children with hemophilia A; perioperative management of patients with hemophilia A; routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults, adolescents

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Tuesday, January 28, 2025

January 28, 2025 at 09:31PM Coronavirus (COVID-19) | CBER-Regulated Biologics

This page and the associated links provide information on guidance and advice relevant to the development of therapies to treat or prevent COVID-19, and contact information for developers seeking additional information or assistance.

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January 28, 2025 at 03:20PM Evolutionary Biologics Inc. - 681586 - 12/30/2024

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

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Friday, January 24, 2025

January 24, 2025 at 04:38PM Webinars and Outreach

CBER sponsored webinars for public and industry.

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Thursday, January 23, 2025

January 23, 2025 at 02:57PM Clinical Guidances

This page lists Clinical Guidance documents.

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January 22, 2025 at 08:15PM Workshops, Meetings & Conferences (Biologics)

Information on CBER sponsored or co-sponsored meetings, conferences and workshops about various biologics in order to educate the public and seek the opinion of interested parties.

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Tuesday, January 21, 2025

January 21, 2025 at 04:50PM Abbott Laboratories - 669353 - 10/24/2023

Dietary Supplement/Adulterated


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Monday, January 20, 2025

January 20, 2025 at 06:30PM FDA Voices

Insights from FDA leadership and experts into the agency's work on policy, consumer safety & enforcement, medical products, food, & tobacco.

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Thursday, January 16, 2025

January 16, 2025 at 07:11PM CBER Rare Disease Program 

Description of CBER's Rare Disease Program, including a description of the program, selected activities, examples of collaborations internal and external to CBER, and frequently asked questions.

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January 16, 2025 at 05:51PM COVID-19 Vaccines

FDA has rigorous scientific and regulatory processes in place to facilitate development and ensure the safety, effectiveness and quality of COVID-19 vaccines.

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January 16, 2025 at 02:59PM Vaccines and Related Biological Products Advisory Committee December 12, 2024 Meeting Announcement - 12/12/2024

This is the main page for the CBER Vaccines and Related Biological Products Advisory Committee (VRBPAC) December 12, 2024 meeting announcement and materials.

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Wednesday, January 15, 2025

January 15, 2025 at 02:41PM Public Webinar: FDA Review of Biologics License Applications for Blood and Source Plasma - 02/19/2025

This webinar is intended to provide blood establishments and other stakeholders with an overview of OBRR’s approach to the review of biologics license applications for the manufacture of blood and blood components, including source plasma. In this event, OBRR staff will give presentations on select topics and address questions submitted by registra

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Tuesday, January 14, 2025

January 14, 2025 at 06:52PM Animal Welfare, Testing and Research of FDA-Regulated Products

FDA-regulated medical and veterinary products save lives. Products undergo different types of testing, including animal testing, to determine their safety and effectiveness. The FDA encourages and accepts scientifically valid alternatives to animal testing.

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January 14, 2025 at 03:40PM Regulatory Harmonization and Convergence

The Agency engages in a range of explicit harmonization initiatives, a subset of which includes the participation of CBER.

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January 14, 2025 at 01:27PM Artificial Intelligence and Machine Learning (AI/ML) for Biological and Other Products Regulated by CBER

Use of Artificial Intelligence and Machine Learning (AI/ML) has rapidly become an important component of everyday life. This includes using AI/ML in the development of Medical Products, including Biologics. This page provides an overview of CBER's activity in AI/ML.

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Monday, January 13, 2025

January 13, 2025 at 07:59PM OCMO Guidance Documents

Guidance documents are intended to assist industry and other interested parties in understanding regulatory expectations, complying with applicable laws, and developing new and innovative products that improve public health.

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January 13, 2025 at 06:22PM Vaccines for COVID-19: A Personal Reflection

Vaccines for Covid-19: A Personal Reflection by Robert M. Califf, MD

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January 13, 2025 at 04:21PM Artificial Intelligence for Drug Development

FDA recognizes the increased use of AI throughout the drug development process and across a range of therapeutic areas. Learn more.

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January 13, 2025 at 03:41PM Devices Guidances

This page lists Medical Device Guidance documents.

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Friday, January 10, 2025

January 10, 2025 at 04:26PM Clinical Investigator Inspection List A-D

Contains names, addresses, and other information gathered from inspections of clinical investigators who have conducted studies with investigational new drugs or investigational devices reviewed by the Center for Biologics Evaluation and Research (CBER).

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January 10, 2025 at 04:25PM Clinical Investigator Inspection List E-K

Contains names, addresses, and other information gathered from inspections of clinical investigators (E-K) who have conducted studies with investigational new drugs or investigational devices reviewed by the Center for Biologics Evaluation and Research (CBER).

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January 10, 2025 at 04:19PM Clinical Investigator Inspection List L-P

Contains names, addresses, and other information gathered from inspections of clinical investigators (L-P) who have conducted studies with investigational new drugs or investigational devices reviewed by the Center for Biologics Evaluation and Research (CBER).

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January 10, 2025 at 04:15PM Clinical Investigator Inspection List Q-S

Clinical Investigator Inspection List from inspections of clinical investigators who have conducted studies with investigational new drugs or investigational devices reviewed by CBER

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Wednesday, January 8, 2025

January 08, 2025 at 07:18PM 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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January 08, 2025 at 05:47PM Administrative Guidances

This page lists Administrative Guidance documents.

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January 08, 2025 at 03:43PM Create and Keep a Medication List for Your Health

Keeping track of when, how and why you use medications is important for your health and safety. A medication list helps you track all the prescription medications, over-the-counter (OTC) drugs, vitamins and supplements that you take. The list can be a lifesaver, especially during an emergency.

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Tuesday, January 7, 2025

January 07, 2025 at 03:20PM XO Biologix, LLC - 697717 - 12/12/2024

Unapproved New Drugs/Adulterated


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January 06, 2025 at 03:41PM Artificial Intelligence-Enabled Device Software Functions: Lifecycle Management and Marketing Submission Recommendations

This draft guidance provides recommendations regarding the contents of marketing submissions for devices that include AI-enabled device software functions.


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January 06, 2025 at 03:41PM Recommendations to Reduce the Risk of Transmission of Mycobacterium tuberculosis (Mtb) by Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)

This is the Guidance for Industry - Recommendations to Reduce the Risk of Transmission of Mycobacterium tuberculosis (Mtb) by Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)

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January 06, 2025 at 01:40PM 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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January 03, 2025 at 02:30AM Biologics Guidances

This page displays links to Biologics Guidance documents.

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January 02, 2025 at 04:55PM Industry Frequently Asked Questions

Frequently asked questions and the associated answers sorted by topic area

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January 02, 2025 at 03:25PM Guidance Agenda: Guidance Documents CBER is Planning to Publish During Calendar Year 2025

This is the list of guidance topics CBER is considering for development during Calendar Year 2025

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