https://www.securitymagazine.com/articles/83539-gao-calls-out-fda-on-medical-device-cyber-security
GAO Calls Out FDA on Medical Device Cyber Security | 2012-10-01 | Security Magazine
The FDA needs to pay more attention during its approval process to the information security of medical devices to ensure they are not easily hacked, according...
fda onmedical devicecyber securitygaocalls
https://www.biospace.com/veru-reaches-agreement-with-fda-on-new-phase-3-clinical-trial-for-sabizabulin-for-broader-indication-hospitalized-adult-patients-with-any-type-of-viral-acute-respiratory-distress-syndrome-ards
Veru Reaches Agreement with FDA on New Phase 3 Clinical Trial for Sabizabulin for Broader...
Sep 26, 2023 - Veru Inc. (NASDAQ: VERU) today announced that in a September 21, 2023 meeting, the Company and FDA reached agreement on the design of a new Phase 3 clinical...
fda onnew phaseclinical trialveruagreement
https://www.sej.org/headlines/whats-name-fda-high-fructose-corn-syrup-says-lots
"What's in a Name? FDA, on High Fructose Corn Syrup, Says Lots" | SEJ
Jun 1, 2012 - "It appears high fructose corn syrup will still be called high fructose corn syrup. On Wednesday, the Food and Drug Administration denied a petition by the...
in afda oncorn syrupnamehigh
https://www.gilead.com/news/news-details/2011/gilead-sciences-receives-refuse-to-file-notification-from-us-fda-on-new-drug-application-for-single-tablet-regimen-of-truvadar-and-tmc278
Gilead Sciences Receives Refuse to File Notification From U.S. FDA on New Drug Application for...
Gilead Sciences Receives Refuse to File Notification From US FDA on New Drug Application for Single Tablet Regimen of TruvadaR and TMC278
gilead sciencesfda onreceivesrefusefile
https://miamicourant.com/advanced-instrumentations-inc-in-miami-inspected-by-fda-on-feb-26-2024/
Advanced Instrumentations, Inc. in Miami inspected by FDA on Feb. 26, 2024 - Miami Courant
Jan 27, 2026 - Advanced Instrumentations, Inc. in Miami underwent an FDA inspection on February 26, 2024, focusing on device compliance and post-market surveillance,...
advanced instrumentationsincmiamifdafeb
https://clpblog.citizen.org/get-more-information-from-the-fda-on-the-relationship-between-pain-drugs-and-heart-attack-and-stroke/
Get more information from the FDA on the relationship between pain drugs and heart attacks and...
Jul 10, 2015 - Many of our readers likely have seen media reports that the Food and Drug Administration (FDA) is strengthening its label warning about the relationship...
get more informationfrom theheart attacksfdarelationship
https://nclnet.org/ncl_comments_to_fda_on_the_overuse_of_antibiotics_in_livestock/
NCL comments to FDA on the overuse of antibiotics in livestock - National Consumers League -...
Dec 14, 2020 - July 12, 2012 Comments of the National Consumers League to the Food and Drug AdministrationComment on Draft Guidance for Industry #213: Docket No....
national consumers leaguenclcommentsfdaoveruse
https://africasmbjournal.com/article/911051172-oculis-announces-agreement-with-fda-on-a-special-protocol-assessment-spa-for-optic-neuritis-registrational-trial
Oculis Announces Agreement with FDA on a Special Protocol Assessment (SPA) for Optic Neuritis...
Africa SMB Journal is an online news publication focusing on sme/smb in the Africa: The best news from Africa on small business
fda onoptic neuritisannouncesagreementspecial
https://www.center4research.org/nchr-testimony-fda-use-abilify-treating-irritability-children-autism/
NCHR Testimony at the FDA on the Use of Abilify for Treating Irritability in Children with Autism -...
Apr 15, 2019 - September 12, 2017. We are particularly concerned about Abilify because of its well established serious side effects of tardive dyskinesia, tremor, muscle...
children with autismthe fdatestimonyuseabilify
https://gfi.org/comment-letters/to-fda-on-labeling-of-plant-based-meat-eggs-and-dairy/
To FDA on labeling of plant-based meat, eggs, and dairy - The Good Food Institute
GFI advocates for clear and simple labeling that would allow for the use of nomenclature consumers like and understand.
eggs and dairygood food institutefda onplant basedlabeling
https://www.goodwinlaw.com/en/insights/publications/2021/10/10_08-california-finally-breaks-from-fda
California Finally Breaks From FDA On CBD: Governor Newsom Signs AB-45
California Finally Breaks From FDA On CBD: Governor Newsom Signs AB-45
fda ongovernor newsomcaliforniafinallybreaks
https://markets.businessinsider.com/news/stocks/okyo-pharma-announces-highlights-from-type-c-meeting-with-fda-on-urcosimod-1035756804
Okyo Pharma announces highlights from Type C meeting with FDA on urcosimod | Markets Insider
type cfda onmarkets insiderpharmaannounces
https://www.tmj4.com/news/addictive-drug-or-alternative-to-break-the-habit-doctors-dispute-fda-about-effects-of-kratom
Doctors challenge FDA on effects of Kratom
Mar 14, 2018 - Is it an addictive drug, or a way to actually overcome addiction? The FDA is considering regulating an herbal drug called Kratom. But a group of doctors is...
fda ondoctorschallengeeffectskratom
https://seattlecitywire.com/chocolate-squirrel-llc-in-seattle-inspected-by-fda-on-june-4-2024/
Chocolate Squirrel, LLC in Seattle inspected by FDA on June 4, 2024 - Seattle City Wire
Feb 15, 2026 - On June 4, 2024, the Food and Drug Administration (FDA) conducted an inspection of Chocolate Squirrel, LLC in Seattle focusing on foodborne biological
squirrel llcfda onchocolateseattlejune
https://www.aans.org/advocacy/articles/neurosurgery-joins-the-alliance-in-sending-letter-to-the-fda-on-regulatory-reduction-2-5-18/
Neurosurgery Joins the Alliance in Sending Letter to the FDA on Regulatory Reduction 2.5.18 - AANS
Apr 30, 2025 - RE: Review of Existing Center for Drug Evaluation and Research Regulatory and InformationCollection Requirements Dear Dr. Gottlieb, The Alliance of
letter to fdathe allianceneurosurgeryjoinssending
https://denvercitywire.com/kroger-mountain-view-foods-company-in-denver-inspected-by-fda-on-june-13-2024/
Kroger Mountain View Foods Company in Denver inspected by FDA on June 13, 2024 - Denver City Wire
Feb 9, 2026 - On June 13, 2024, the Food and Drug Administration conducted an inspection of Kroger Mountain View Foods Company in Denver, focusing on foodborne
mountain viewfda onkrogerfoodscompany
https://www.lupus.org/es/node/5482/chapter/18
Lupus Foundation of America Engages FDA on Inclusion of Pregnant and Breastfeeding Women in...
The Lupus Foundation of America Engages the Food and Drug Administration on Inclusion of Pregnant and Breastfeeding Women in Clinical Trials.
of americafda onlupusfoundationengages
https://blog.ucs.org/gretchen-goldman/where-is-the-fda-on-social-media-and-science-668/
Where Is the FDA on Social Media and Science? - Union of Concerned Scientists
Nov 22, 2022 - Last week, we released an update to Grading Government Transparency, a report we first released in 2013. The report assesses the media policies and social...
on social mediawhere isthe fdaand scienceunion
https://www.tpr.org/2020-10-22/group-of-independent-experts-to-advise-fda-on-coronavirus-vaccine-approval
Group Of Independent Experts To Advise FDA On Coronavirus Vaccine Approval | TPR
Oct 22, 2020 - An advisory committee to the Food and Drug Administration will hear the agency's plans for approving a coronavirus vaccine and provide advice for modifying...
fda oncoronavirus vaccinegroupindependentexperts
https://radio.wpsu.org/2006-04-21/fda-on-medical-marijuana-science-or-politics
FDA on Medical Marijuana: Science or Politics? | WPSU
May 17, 2022 - The Food and Drug Administration declares that there is no medical use for marijuana. The determination returns the FDA to the middle of a politics vs. science...
fda onmedical marijuanasciencepoliticswpsu
https://www.cspi.org/press-release/cspi-seeks-update-fda-poppy-petition
CSPI seeks update from FDA on poppy petition
Nov 24, 2025 - A year ago the Center for Science in the Public Interest urged the Food and Drug Administration to protect consumers from unprocessed poppy seeds contaminated...
fda oncspiseeksupdatepoppy
https://ahrp.org/vioxx-redux-fda-on-the-sidelines-as-marketing-subsumes-evidence-surviving-sepsis-nejm/
Vioxx Redux: FDA on the Sidelines as Marketing Subsumes Evidence: Surviving Sepsis-NEJM | Alliance...
Nov 22, 2014 - Lilly's aggressive marketing of Xigris does indeed epitomize the worst ofthis industry's mission.
fda onvioxxreduxsidelinesmarketing
https://www.nmpf.org/may-29-u-s-dairy-groups-ask-fda-not-to-use-same-imported-food-safety-oversight-for-dairy-as-being-applied-to-foreign-shellfish/attachment-letter-to-fda-on-equivalence_nmpf-usdec_final-052918/
Letter-to-FDA-on-Equivalence_NMPF-USDEC_Final-052918 - NMPF
Dec 3, 2018 - Letter-to-FDA-on-Equivalence_NMPF-USDEC_Final-052918
letter to fdaequivalencefinal
https://www.dailyintakeblog.com/2021/11/ags-petition-fda-on-baby-food-heavy-metal-limits/
AGs Petition FDA on Baby Food Heavy Metal Limits | The Daily Intake
Feb 27, 2023 - On October 21, 2021, a coalition of 23 Attorneys General petitioned FDA to expedite setting heavy metal standards for baby foods. The petition echoes
fda onbaby foodheavy metalthe dailyags
https://nvca.org/document/comment-letter-to-fda-on-alternative-approval-pathway-2-27-14-2/
NVCA Comment Letter to FDA on Alternative Approval Pathway - National Venture Capital Association -...
Aug 26, 2025 - Advocates for flexible approval processes for emerging therapies.
letter to fdaventure capitalcommentalternativeapproval
https://www.wbrz.com/news/lsu-grad-files-for-patent-working-with-fda-on-drug-to-stop-covid-19
LSU grad files for patent, working with FDA on drug to stop COVID-19
A Baton Rouge native and LSU grad said scientists working for her company have found a drug that is showing promise in laboratories at blocking the continued...
working withfda onstop covidlsugrad
https://www.cahill.com/news/firm-news/101454
Cahill Wins Appeal Against the FDA on Behalf of Lorillard Tobacco Company | Cahill Gordon & Reindel...
A Cahill litigation team prevailed on behalf of the Lorillard Tobacco Company in an appeal by the U.S. Food and Drug Administration ("FDA"),
the fdacahillwinsappealbehalf
https://www.acr.org/News-and-Publications/acr-provides-input-to-fda-on-ai-measurement-and-evaluation
ACR Provides Input to FDA on AI Measurement and Evaluation
ACR submitted comments to FDA on real-world AI device performance, stressing safety, governance, and continuous monitoring.
measurement and evaluationacrprovidesinputfda
https://www.directsellingnews.com/2019/09/19/dsa-seeks-clarity-from-fda-on-cbd-products/
DSA Seeks Clarity from FDA on CBD Products - Direct Selling News
fda oncbd productsdirect sellingdsaseeks
https://foodpoisoningbulletin.com/2025/fda-on-lyons-and-sysco-shakes-deadly-listeria-outbreak/
FDA On Lyons and Sysco Shakes Deadly Listeria Outbreak
May 17, 2025 - FDA weighs in on the Lyons and Sysco Shakes deadly Listeria monocytogenes outbreak that has sickened 42 people and killed 14.
fda onlyonssyscoshakesdeadly
https://www.army.mil/article/231464/army_collaborates_with_fda_on_advanced_manufacturing_3d_printing
Army collaborates with FDA on advanced manufacturing, 3D printing | Article | The United States Army
Jan 9, 2020 - As the Army embraces advanced manufacturing in its modernization strategies, medical logisticians are looking to 3D printing as a potential solution to ensure...
the united statesfda onadvanced manufacturingarmycollaborates
https://societyfp.org/sfp-letter-to-the-fda-on-the-risk-evaluation-and-mitigation-strategy-rems-for-mifepristone/
SFP letter to the FDA on the Risk Evaluation and Mitigation Strategy (REMS) for mifepristone -...
Jun 14, 2022 - The Society of Family Planning is the source for abortion and contraception science.
to thefda onrisk evaluationsfpletter
https://www.americantelemed.org/policies/ata-action-letter-to-cms-and-fda-on-access-model-tempo-programs/
ATA Action Letter to CMS and FDA on ACCESS Model & TEMPO Programs - ATA
fda onataactionlettercms
https://www.iowaindependent.com/fast-news/fda-flags-popular-philippine-sauces-for-additives-causing-supply-concerns-on-guam/
FDA Flags Popular Philippine Sauces for Additives, Causing Supply Concerns on Guam - The Iowa...
Nov 5, 2024 - The U.S. Food and Drug Administration (FDA) has recently flagged several popular Filipino sauces for containing "harmful" additives, raising alarms among Filipi
fdaflagspopularphilippinesauces
https://wbjournal.com/article/bsx-wins-fda-approval-on-heart-devices/
BSX wins FDA approval on heart devices
Apr 16, 2014 - Natick-based Boston Scientific Corp. (BSX) has received approval for its newest defibrillators and heart failure devices, including the trademarked Dynagen...
fda approvalbsxwinsheartdevices
https://ducknetweb.blogspot.com/2010/10/group-of-house-of-representatives-sends.html
Group of House of Representatives Sends Letter to FDA Wanting More Transparency and Detail on...
This is pretty much a no brainer in concept as many of the new devices and what is being approved revolves around software, thus they might ...
letter to fdagrouphouserepresentativessends