9/15/2023 |
2023 Biological License Application Approvals
Updated through 8/31/2023 |
9/15/2023 |
2023 Biological Device Application Approvals
Updated through 8/31/2023 |
9/15/2023 |
Labeling for Biosimilar and Interchangeable Biosimilar Products; Draft Guidance for Industry |
9/15/2023 |
Annual Status Report Information and Other Submissions for Postmarketing Requirements and Commitments: Using Forms FDA 3988 and FDA 3989; Guidance for Industry |
9/14/2023 |
OTP Learn
Updated: Overview of Office of Therapeutic Products (OTP) Regulated Products video |
9/14/2023 |
Clinical Reviewer - ALBUMINEX |
9/14/2023 |
Breakthrough Devices Program; Guidance for Industry and Food and Drug Administration Staff |
9/14/2023 |
September 12, 2023 Summary Basis for Regulatory Action - ABRYSVO |
9/13/2023 |
Chemistry, Manufacturing, and Controls Development and Readiness Pilot (CDRP) Program
Updated: FDA will begin accepting requests to participate in year two of the CDRP on October 2, 2023. |
9/13/2023 |
CBER Title 21 Vacancy Announcement – Program Analyst, AD-0343, Bands A/B, Office of Management (OM), Division of Management and Planning Analysis (DMPA), Capacity Planning and Management Analysis Branch (CPMAB) |
9/13/2023 |
September 11, 2023 Approval Letter - BIVIGAM |
9/13/2023 |
September 11, 2023 Approval Letter - ASCENIV |
9/11/2023 |
September 11, 2023 Approval Letter - SPIKEVAX |
9/11/2023 |
September 11, 2023 Approval Letter COMIRNATY |
9/11/2023 |
Warrior Families: Advancing Regenerative Medicine Through Science |
9/11/2023 |
CBER Vacancy: Staff Fellow/Visiting Associate – Parasitic Diseases |
9/11/2023 |
Institutional Review Board (IRB) Review of Individual Patient Expanded Access Submissions for Investigational Drugs and Biological Products; Guidance for IRBs and Clinical Investigators |
9/11/2023 |
BK230961 - AQUIOS CL Flow Cytometer and AQUIOS Stem Kit |
9/11/2023 |
CBER Cures Vacancy Announcement - Biologist, AD-0401-Band C, Office of Vaccines Research and Review (OVRR), Division of Vaccines and Related Product Applications (DVRPA) |
9/8/2023 |
Center for Biologics Evaluation and Research Patient Engagement Program
Updated to include additional resources |
9/8/2023 |
OTP Town Hall: Nonclinical Assessment of Cell and Gene Therapy Products
Updated to include the event recording. |
9/7/2023 |
Use of International Standard ISO 10993-1, "Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process"; Guidance for Industry and Food and Drug Administration Staff |
9/7/2023 |
Application of Human Factors Engineering Principles for Combination Products: Questions and Answers; Guidance for Industry and FDA Staff |
9/7/2023 |
Cellular, Tissue, and Gene Therapies Advisory Committee October 31, 2023 Meeting Announcement |
9/6/2023 |
DSCSA Standards for the Interoperable Exchange of Information for Tracing of Certain Human, Finished, Prescription Drugs; Guidance for Industry |
9/6/2023 |
Important Information for Human Cell, Tissue and Cellular and Tissue-based Product (HCT/P) Establishments Regarding Tuberculosis Outbreaks Linked to a Bone Matrix Product |
9/6/2023 |
Best Practices for Selecting a Predicate Device to Support a Premarket Notification [510(k)] Submission; Draft Guidance for Industry and Food and Drug Administration Staff |
9/6/2023 |
Recommendations for the Use of Clinical Data in Premarket Notification [510(k)] Submissions; Draft Guidance for Industry and Food and Drug Administration Staff |
9/6/2023 |
Evidentiary Expectations for 510(k) Implant Devices; Draft Guidance for Industry and Food and Drug Administration Staff |
9/5/2023 |
CBER Vacancy: Staff Fellow/Visiting Associate - Pharmacology/Toxicology Reviewer |
9/5/2023 |
Clinical Pharmacology Review - ATGAM |
9/1/2023 |
Complete List of Licensed Products and Establishments
Updated as of 8/31/2023 |
9/1/2023 |
Complete List of Substantially Equivalent 510(k) Device Applications
Updated as of 8/31/2023 |
9/1/2023 |
Complete List of Currently Approved Premarket Approvals (PMAs)
Updated as of 8/31/2023 |
9/1/2023 |
Complete List of Currently Approved NDA and ANDA Application Submissions
Updated as of 8/31/2023 |
8/31/2023 |
Considerations for the Use of Real-World Data and Real-World Evidence To Support Regulatory Decision-Making for Drug and Biological Products; Guidance for Industry |
8/30/2023 |
2023 PDA/ FDA Joint Regulatory Conference |
8/30/2023 |
Wholesale Distributor Verification Requirement for Saleable Returned Drug Product and Dispenser Verification Requirements When Investigating a Suspect or Illegitimate Product—Compliance Policies; Guidance for Industry |
8/30/2023 |
Enhanced Drug Distribution Security at the Package Level Under the Drug Supply Chain Security Act; Guidance for Industry |
8/30/2023 |
CBER Cures Vacancy Announcement - Physician (Gastroenterology), AD-0602-Band C, Office of Therapeutic Products (OTP), Office of Clinical Evaluation (OCE) |
8/29/2023 |
Vaccine Facts: Why you and your Family Need Vaccines |
8/28/2023 |
CBER Rare Disease Program |
8/25/2023 |
August 9, 2023 Approval Letter - ADYNOVATE |
8/25/2023 |
Enhanced Drug Distribution Security Requirements Under Section 582(g)(1) of the Federal Food, Drug, and Cosmetic Act--Compliance Policies; Guidance for Industry |
8/24/2023 |
Assessing Genetic Heterogeneity in the Context of Genome Editing Off-Targets in Gene Therapy Products: An FDA Public Workshop |
8/24/2023 |
Vaccines and Related Biological Products Advisory Committee October 5, 2023 Meeting Announcement |
8/24/2023 |
August 23, 2023 Approval Letter - ATGAM |
8/23/2023 |
August 21, 2023 Approval Letter - VARIVAX |
8/23/2023 |
August 21, 2023 Approval Letter - ProQuad |
8/23/2023 |
August 21, 2023 Approval Letter - ABRYSVO (STN 125769/26) |
8/21/2023 |
August 21, 2023 Approval Letter - ABRYSVO (STN 125768) |
8/21/2023 |
Postmarketing Approaches to Obtain Data on Populations Underrepresented in Clinical Trials for Drugs and Biological Products; Draft Guidance for Industry |
8/18/2023 |
eSubmitter Application History |