Food recalls in America regulated by FDA in 2019 by GAO Xiufen, YANG Dajin

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Thoracic Endovascular Aortic Repair Adverse Events Reported In The Food And Drug Administration Manufacturer And User Facility Device Experience Database by Mansukhani NA, Haleem MS, Eskandari MK

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Why the Watchdog Won’t Bite: U.S. Food and Drug Administration Challenges by Joe Lex

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Medical Economics: End the FDA (Food and Drug Administration) by John Romanach, Walter E. Block

Subjects: “…food and drug administration…”
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New science, drug regulation, and emergent public health issues: The work of FDA’s division of applied regulatory science by Kimberly Chiu, Rebecca Racz, Keith Burkhart, Jeffry Florian, Kevin Ford, M. Iveth Garcia, Robert M. Geiger, Kristina E. Howard, Paula L. Hyland, Omnia A. Ismaiel, Naomi L. Kruhlak, Zhihua Li, Murali K. Matta, Kristin W. Prentice, Kristin W. Prentice, Aanchal Shah, Aanchal Shah, Lidiya Stavitskaya, Donna A. Volpe, James L. Weaver, Wendy W. Wu, Rodney Rouse, David G. Strauss

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Regulation of Neurological Devices and Neurointerventional Endovascular Approaches for Acute Ischemic Stroke by Christopher M. Loftus, Michael Hoffmann, William Heetderks, Xiaolin Zheng, Carlos Peña

Subjects: “…Food and Drug Administration…”
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Sustained virological response rates with direct-acting antivirals in black subjects with HCV genotype 1 infection: systematic analysis of clinical trials by Kimberly Struble, Kirk Chan-Tack, Karen Qi, Thamban Valappil, Sarah Connelly, Poonam Mishra, Dionne Price, Jeffrey Murray, Debra Birnkrant

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Characteristics of pivotal clinical trials of FDA-approved endovascular devices between 2000 and 2018: An interrupted time series analysis by John T. Moon, Menelaos Konstantinidis, Nevon Song, Nariman Nezami, Bill S. Majdalany, Allen Herr, Gary Siskin

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Predicting factors for the pattern of intravenous immunoglobulin utilization in a middle eastern university hospital by Zeinab Fakhari, Shadi Farsaei, Ali Mohammad Sabzghabaee

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Characterization of US Food and Drug Administration Class I Recalls from 2018 to 2022 for Moderate- and High-Risk Medical Devices: A Cross-Sectional Study by Mooghali M, Ross JS, Kadakia KT, Dhruva SS

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The Conundrum of Online Prescription Drug Promotion Comment on “Trouble Spots in Online Direct-to-Consumer Prescription Drug Promotion: A Content Analysis of FDA Warning Letters”... by Isaac Wanasika

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Exploring digital therapeutics: The next paradigm of modern health-care industry by Raj Khirasaria, Vikramjit Singh, Angelika Batta

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Development of Celiac Disease Therapeutics: The Sixth Gastroenterology Regulatory Endpoints and the Advancement of Therapeutics Workshop by Irena Lavine, Suna Seo, Juli Tomaino

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Drug flibanserin–in hypoactive sexual desire disorder by Pugazhenthan Thangaraju, Hemasri Velmurugan, Sree Sudha TY

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Biosimilars in India; current status and future perspectives by Bikash R Meher, Sakthi Balan, Rashmi R Mohanty, Monalisa Jena, Smita Das

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Evaluation of rational prescription pattern of intravenous immunoglobulin (IVIG) based on FDA-approved indications among teaching hospitals in Birjand by Abolfazl Abbaszadeh, Mohammad Ali Mahdiabadi, Seyed Mohammad Riahi, Razieh Avan

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Biosimilar insulins – What a clinician needs to know? by Sujoy Ghosh, Saptarshi Bose, Sandeep Gowda, Pradip Mukhopadhyay

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‘Testosterone Boosting’ Supplements Composition and Claims Are not Supported by the Academic Literature by Chase G. Clemesha, Hatim Thaker, Mary K. Samplaski

Subjects: “…united states food and drug administration…”

Beyond the Present Constraints That Prevent a Wide Spread of Tissue Engineering and Regenerative Medicine Approaches by Benjamen T. O'Donnell, Clara J. Ives, Omair A. Mohiuddin, Omair A. Mohiuddin, Bruce A. Bunnell, Bruce A. Bunnell

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The primary entries in the Reportable Food Registry by Marcin Pigłowski

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