June 30, 2021 at 08:14PM MACI (Autologous Cultured Chondrocytes on a Porcine Collagen Membrane)

MACI (autologous cultured chondrocytes on porcine collagen membrane) is an autologous cellularized scaffold product indicated for the repair of single or multiple symptomatic, full-thickness cartilage defects of the knee with or without bone involvement in adults.

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June 28, 2021 at 09:18PM BabyBIG

Product approval information is indicated for Treatment of infant botulism caused by type A or type B in patients below one year of age.

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June 28, 2021 at 01:14PM FDA and Industry Procedures for Section 513(g) Requests for Information under the Federal Food, Drug, and Cosmetic Act

This guidance establishes procedures for submitting, reviewing and responding to 513(g) requests for information regarding the classification and the regulatory requirements that may be applicable to a particular device.

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June 26, 2021 at 02:25AM Learn More About COVID-19 Vaccines From the FDA

Get answers to your questions about the standards for safety and effectiveness to support an emergency use authorization of COVID-19 vaccines.

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June 25, 2021 at 07:40PM Learn About FDA Patient Engagement

Learn about the different ways that patients and caregivers are working with the FDA to have their voice included in medical product approvals and FDA policy.

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June 25, 2021 at 04:51PM Clinical Guidances

This page lists Clinical Guidance documents.

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June 25, 2021 at 02:50PM Sponsor Responsibilities - Safety Reporting Requirements and Safety Assessment for IND and Bioavailability/Bioequivalence Studies

Sponsor Responsibilities - Safety Reporting Requirements and Safety Assessment for IND and Bioavailability/Bioequivalence Studies

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June 24, 2021 at 03:08PM Cancer Clinical Trial Eligibility Criteria: Available Therapy in Non-Curative Settings

This guidance provides recommendations to clinical investigators and sponsors regarding the inclusion of patients who have not received available therapy for their cancer in clinical trials of drugs and biological products for the treatment of cancer in the non-curative setting.

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Wednesday, June 23, 2021

June 23, 2021 at 09:46PM Application Submissions Guidances

This page lists Application Submissions Guidance documents.

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June 23, 2021 at 08:28PM COVID-19: Developing Drugs and Biological Products for Treatment or Prevention

COVID-19: Developing Drugs and Biological Products for Treatment or Prevention

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June 23, 2021 at 05:10PM COVID-19: Master Protocols Evaluating Drugs and Biological Products for Treatment or Prevention

COVID-19: Master Protocols Evaluating Drugs and Biological Products for Treatment or Prevention

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June 22, 2021 at 06:15PM Vaccines, Blood & Biologics

From blood to vaccines, FDA protects and advances the public health by ensuring that biological products are safe, effective, and available to those who need them. Read these Consumer Updates to learn more.

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Monday, June 21, 2021

June 21, 2021 at 10:24PM Devices Guidances

This page lists Medical Device Guidance documents.

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Thursday, June 17, 2021

June 17, 2021 at 09:51PM BIMO/Team Biologics/Internet Surveillance/Other

This is the main page for the CBER BIMO/Team Biologics/Internet Surveillance/Other.

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June 15, 2021 at 04:37PM Premenopausal Women with Breast Cancer: Developing Drugs for Treatment

This guidance provides recommendations to sponsors developing drugs or biological products regulated by CDER and CBER for the treatment of breast cancer.

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June 15, 2021 at 03:35PM Have You Given Blood Lately?

FDA works to ensure the safety of the more than 14 million units of blood and blood components donated in the U.S. each year. Learn how FDA helps safeguard the blood supply and how you can donate blood.

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Wednesday, June 16, 2021

June 17, 2021 at 03:06AM 2021_06 Test Article FT 02

2021_06 Test Article FT 02

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June 15, 2021 at 02:22PM ADYNOVATE

Product approval information is indicated for children and adults with hemophilia A (congenital factor VIII deficiency) for: (1) On-demand treatment and control of bleeding episodes; (2) Perioperative management; (3) Routine prophylaxis to reduce the frequency of bleeding episodes.

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June 16, 2021 at 02:25PM Complete List of Donor Screening Assays for Infectious Agents and HIV Diagnostic Assays

Links to the different types of Donor Screening Assays. A table for each assay is provided with detailed information such as tradename, infectious agent, format, specimen, use, manufacturer, approval date, and STN.

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Tuesday, June 15, 2021

June 16, 2021 at 12:54AM Coronavirus (COVID-19) Update: June 15, 2021

Coronavirus (COVID-19) Update: June 15, 2021

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June 15, 2021 at 10:42PM STRATAGRAFT

For the treatment of adults with thermal burns containing intact dermal elements for which surgical intervention is clinically indicated (deep partial-thickness burns)

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Monday, June 14, 2021

June 14, 2021 at 04:09PM Human Cell and Tissue Establishment Registration (HCTERS) Public Query Application

Welcome to the Human Cell and Tissue Establishment Registration (HCTERS) Public Query application. You may use this application to review Human Cell and Tissue registration information for registered, inactive, and pre-registered firms.

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June 12, 2021 at 12:22AM KYMRIAH (tisagenlecleucel)

KYMRIAH is a CD19-directed genetically modified autologous T cell immunotherapy indicated for the treatment of patients up to 25 years of age with B-cell precursor acute lymphoblastic leukemia (ALL) that is refractory or in second or later relapse

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June 11, 2021 at 05:56PM Labeling and Promotion Guidances

This page lists Labeling and Promotion Guidance documents.

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June 11, 2021 at 04:56PM Testing for Biotin Interference in In Vitro Diagnostic Devices

Testing for Biotin Interference in In Vitro Diagnostic Devices, Guidance for Industry, Final, CBER, Biologics

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Thursday, June 10, 2021

June 10, 2021 at 08:14PM Developing a Toolkit to Assess Efficacy of Ebola Vaccines and Therapeutics

MCMi regulatory science project to research issues that are key to understanding and predicting if—and how—vaccines and therapeutics to prevent and treat Ebola will show efficacy

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Wednesday, June 9, 2021

June 09, 2021 at 08:37PM Donate COVID-19 Plasma

If you have fully recovered from COVID-19, you may be able to help patients currently fighting the infection by donating your plasma. Because you fought the infection, your plasma now contains COVID-19 antibodies.

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June 09, 2021 at 08:22PM Guidance Agenda: Guidance Documents CBER is Planning to Publish During Calendar Year 2021

This is the list of guidance topics CBER is considering for development during Calendar Year 2021.

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June 08, 2021 at 08:35PM Moderna COVID-19 Vaccine

Information about the Moderna COVID-19 Vaccine

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June 09, 2021 at 04:08PM Vaccines Licensed for Use in the United States

The product name and trade name of vaccines licensed for use in the United States.

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June 09, 2021 at 02:56PM Core Patient-Reported Outcomes in Cancer Clinical Trials

This guidance provides recommendations to sponsors for collection of a core set of patient-reported clinical outcomes in cancer clinical trials and related considerations for instrument selection and trial design.

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Tuesday, June 8, 2021

June 08, 2021 at 10:20PM Coronavirus (COVID-19) Update: June 8, 2021

Coronavirus (COVID-19) Update: June 8, 2021

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June 08, 2021 at 08:22PM Recalls (Biologics)

Biologic recalls are listed by year. Recalls are a firm's removal or correction of a marketed product that the FDA considers to be in violation of the laws it administers and against which the agency would initiate legal action.

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June 08, 2021 at 07:46PM 2018 Biologics Recalls

2018 Biologics Recalls

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June 08, 2021 at 03:24PM Executive Order 14017 on America’s Supply Chains

Updates on recommendations to help shore up the U.S. pharmaceutical supply chain, as directed by Executive Order 14017 on America’s Supply Chains

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Monday, June 7, 2021

June 07, 2021 at 05:55PM JYNNEOS

Indicated for prevention of smallpox and monkeypox disease in adults 18 years of age and older determined to be at high risk for smallpox or monkeypox infection.


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June 07, 2021 at 04:07PM RIASTAP

Product approval information is indicated for the treatment of acute bleeding episodes in patients with congenital fibrinogen deficiency, including afibrinogenemia and hypofibrinogenemia (1). RiaSTAP is not indicated for dysfibrinogenemia.

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June 07, 2021 at 03:00PM Vaccine EUA Questions and Answers for Stakeholders

Questions and answers about vaccine Emergency Use Authorizations for stakeholders including industry, health care providers, pharmacists, and state, local, tribal, and territorial governments

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Friday, June 4, 2021

June 04, 2021 at 11:51PM Approved Cellular and Gene Therapy Products

Listing of licensed and approved products from the Office of Tissues and Advanced Therapies (OTAT).

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June 04, 2021 at 09:02PM FDALabel: Full-Text Search of Drug Product Labeling

FDALabel Database is a web-based application that allows users to perform customizable searches of a database containing over 130,000 labeling documents for FDA-approved drug products, including human and animal prescription and over-the-counter drugs, biological products, and medical devices.

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June 04, 2021 at 07:51PM 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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June 04, 2021 at 07:28PM Animal Rule Information

Links to information about the Animal Rule, which may be used to grant marketing approval of certain products when human challenge studies would not be ethical or feasible

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June 04, 2021 at 07:08PM Roster of the Cellular, Tissue and Gene Therapies Advisory Committee

This is the Roster of the Cellular, Tissue and Gene Therapies Advisory Committee.

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June 04, 2021 at 02:55PM Biologics PREA Reviews and Labeling Changes

PREA Labeling Changes, Medical, Statistical, and Clinical Pharmacology Reviews of Pediatric Studies Conducted under Section 505B of the Federal Food, Drug, and Cosmetic Act (the Act), as amended by the FDA Amendments Act of 2007 (FDAAA). These assessments are for CBER regulated drugs approved under section 505 of the Act and biological drugs licensed under section 351 of the Public Health Service Act.

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June 04, 2021 at 02:35PM Medical Countermeasure Monitoring and Assessment

FDA guidance and regulatory information, specific FDA projects related to monitoring and assessment of MCMs, ongoing FDA work related to medical product assessment in general, and key efforts relevant to MCM monitoring and assessment outside of FDA

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Thursday, June 3, 2021

June 04, 2021 at 01:55AM 2021_06 Test Article FT 01

2021_06 Test Article some long description some long description.

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June 03, 2021 at 05:43PM Innovative Regenerative Medicine Therapies – Patient Safety Comes First

Cellular-derived therapies, including stem cell-based products, offer the potential to treat or even cure diseases or conditions for which few effective treatment options exist.

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June 02, 2021 at 11:35PM Consumers (Biologics)

Resources for consumers on biological products.

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June 03, 2021 at 03:56PM Important Patient and Consumer Information About Regenerative Medicine Therapies

There continues to be broad marketing of unapproved products considered regenerative medicine therapies that are intended for the treatment or cure of a wide range of diseases or medical conditions. These products require FDA licensure/approval to be marketed to consumers.

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June 02, 2021 at 11:57PM Resources for You (Biologics)

Biological products include a wide range of products such as vaccines, blood and blood components, allergenics, somatic cells, gene therapy, tissues, and recombinant therapeutic proteins.

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June 01, 2021 at 07:09PM Roster of the Vaccines and Related Biological Products Advisory Committee

This is the Roster of the Vaccines and Related Biological Products Advisory Committee

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June 01, 2021 at 08:41PM FDA Voices on Medical Products

FDA Voices on Medical Products

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June 01, 2021 at 03:20PM Utah Cord Bank LLC - 614021 - 05/11/2021

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


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