12/6/2019 | Public Safety Notification on Exosome Products |
12/5/2019 | December 3, 2019 Approval Letter - Panoscreen EXTEND |
12/5/2019 | User Fee Billable Biologic Products and Potencies Approved Under Section 351 of PHS Act |
12/5/2019 | Influenza Vaccine for the 2019-2020 Season |
12/5/2019 | Job Vacancy Announcement: Physician, Division of Epidemiology (DE) - Title 38(F) Physician (GP-0602) |
12/4/2019 | December 3, 2019 Approval Letter - Data-Cyte Plus 2, and Data-Cyte Extend 0.8 % Reagent Red Blood Cells |
12/4/2019 | BK190389 - ALBAcheck BGS Monoclonal Control |
12/3/2019 | November 25, 2019 Untitled Letter - Chara Biologics, Inc. |
12/3/2019 | Exceptions and Alternative Procedures Approved Under 21 CFR 640.120 |
12/2/2019 | March 3, 2020 Workshop - Facilitating End-to-End Development of Individualized Therapeutics |
11/29/2019 | November 26, 2019 Approval Letter - Pneumovax 23 |
11/27/2019 | November 25, 2019 Order to Cease Manufacturing - Gynecology, Reproductive Endocrinology and Fertility Institute (GREFI) |
11/27/2019 | Influenza Vaccine for the 2019-2020 Season |
11/25/2019 | FDA Zika virus reference panel for molecular-based diagnostic devices supports product testing for Emergency Use Authorization and 510(k) submissions |
11/22/2019 | November 20, 2019 Untitled Letter - RichSource Stem Cells, Inc. |
11/21/2019 | Influenza Vaccine for the 2019-2020 Season |
11/18/2019 | 2019 Biological Device Application Approvals |
11/18/2019 | 2019 Biological New Drug Application (NDA) and Abbreviated New Drug Application (ANDA) Approvals |
11/18/2019 | November 7, 2019 - Anti-Fyb (Murine Monoclonal) (Recombinant) |
11/18/2019 | November 7, 2019 - Anti-Fya (Murine Monoclonal) (Recombinant) |
11/15/2019 | SOPP 8116: Use of Electronic Signatures for Regulatory Documents |
11/14/2019 | Influenza Vaccine for the 2019-2020 Season |
11/13/2019 | November 12, 2019 Approval Letter - Rotarix |
11/13/2019 | CBER-Regulated Products: Current Shortages |
11/12/2019 | BK190349 - RD2 System |
11/7/2019 | BK190406 - Arthrex Double Syringe (ACP) kit |
11/7/2019 | BK180296 - Fidia PRP Kit |
11/6/2019 | Vaccines and Related Biological Products Advisory Committee November 8, 2019 Meeting Discussion Topics |
11/6/2019 | November 6, 2019 Approval Letter - INFANRIX |
11/6/2019 | November 6, 2019 Approval Letter - PEDIARIX |
11/6/2019 | November 6, 2019 Approval Letter - KINRIX |
11/5/2019 | November 5, 2019 Grant Order - Sentosa SQ HIV-1 Genotyping Assay |
11/5/2019 | Instructions for Using the Electronic Human Cell and Tissue Establishment Registration System (eHCTERS) |
11/4/2019 | November 4, 2019 Approval Letter - Fluzone High-Dose Quadrivalent |
11/4/2019 | SOPP 8101.1: Regulatory Meetings with Sponsors and Applicants for Drugs and Biological Products |
11/4/2019 | Complete List of Currently Approved NDA and ANDA Application Submissions |
11/4/2019 | Complete List of Currently Approved Premarket Applications (PMAs) |
11/4/2019 | Complete List of Substantially Equivalent 510(k) Device Applications |
11/4/2019 | Complete List of Licensed Products and Establishments |
10/31/2019 | Use of Fecal Microbiota for Transplantation to Treat Clostridium difficile - Agenda |
10/29/2019 | Exceptions and Alternative Procedures Approved Under 21 CFR 640.120 |
10/28/2019 | October 25, 2019 Approval Letter - IMOVAX |
10/28/2019 | 2019 Biological License Application Supplement Noteworthy Approvals |
10/28/2019 | 2019 Biological License Application Approvals |
10/28/2019 | 2019 Biological New Drug Application (NDA) and Abbreviated New Drug Application (ANDA) Approvals |
10/28/2019 | 2019 Biological Device Application Approvals |
10/25/2019 | October 25, 2019 Approval Letter - ANTICOAGULANT SODIUM CITRATE 4% w/v SOLUTION, USP |
10/25/2019 | Use of Fecal Microbiota for Transplantation to Treat Clostridium difficile - Agenda |
10/25/2019 | October 24, 2019 Approval Letter - BEXSERO |
10/24/2019 | CBER-Regulated Products: Resolved Shortages |
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