Fri.Aug 30, 2024

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Ozempic, Wegovy Have Health Benefits Beyond Weight Loss, Studies Find

Drugs.com

FRIDAY, Aug.30, 2024 -- New trials are showing how the blockbuster diabetes and weight-loss meds Ozempic and Wegovy can boost health in even more ways.These two injected drugs are versions of semaglutide. In multiple new data analyses, the drugs.

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Morphing facial technology sheds light on the boundaries of self-recognition

Science Daily: Pharmacology News

Facial recognition is a critical part of self-image and social interactions. In an era of advanced digital technology, we face intriguing questions about communication and identity. How does altering our facial identity affect our sense of 'self' and our interactions with others?

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Antibiotic Overuse in Nursing Homes Could Foster 'Superbugs'

Drugs.com

FRIDAY, Aug. 30, 2024 -- Senior residential homes are breeding grounds for antibiotic-resistant bacteria, due to overprescription of antibiotics, a new study says.Stool samples provided by Australian senior home residents contained bacteria with a.

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Labor Day Message 2024

NIOSH Science Blog: Drugs

Each Labor Day we honor workers and the role they play in building a strong and prosperous nation. Much like the first Labor Day more than a century ago, many of us mark this federal holiday with festivities such as parades or picnics. This year, as you head out to celebrate the end of summer with friends and loved ones, I urge you to take a moment to reflect on the contributions of the workers all around us.

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From Diagnosis to Delivery: How AI is Revolutionizing the Patient Experience

Speaker: Simran Kaur, Founder & CEO at Tattva Health Inc.

The healthcare landscape is being revolutionized by AI and cutting-edge digital technologies, reshaping how patients receive care and interact with providers. In this webinar led by Simran Kaur, we will explore how AI-driven solutions are enhancing patient communication, improving care quality, and empowering preventive and predictive medicine. You'll also learn how AI is streamlining healthcare processes, helping providers offer more efficient, personalized care and enabling faster, data-driven

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Buying Smokes? Everyone Under 30 Now Must Show ID

Drugs.com

FRIDAY, Aug. 30, 2024 -- A new, tougher rule on the sale of tobacco products will require retailers to check the IDs of any buyers under the age of 30, the U.S. Food and Drug Administration announced Thursday.The final rule, which will go into.

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Genomic dark matter solves butterfly evolutionary riddle

Science Daily: Pharmacology News

Researchers have uncovered a surprising genetic mechanism that influences the vibrant and complex patterns on butterfly wings. The team discovered that an RNA molecule, rather than a protein as previously thought, plays a pivotal role in determining the distribution of black pigment on butterfly wings.

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What a submerged ancient bridge discovered in a Spanish cave reveals about early human settlement

Science Daily: Pharmacology News

Geologists examined a submerged 25-foot bridge to tackle a long-lasting archaeological controversy: When humans settled on the islands in the western Mediterranean. Their findings narrow a historical gap between the settlement timelines of the eastern and western Mediterranean regions.

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Depression Might Sometimes Be Early Sign of Alzheimer's Disease

Drugs.com

FRIDAY, Aug. 30, 2024 -- In some people, new-onset depression may stem from the same buildup of toxic plaques in the brain that have long been linked to Alzheimer's disease, according to a new study."Our findings provide additional support for.

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Doughnut-shaped region found inside Earth's core deepens understanding of planet's magnetic field

Science Daily: Pharmacology News

A doughnut-shaped region thousands of kilometers beneath our feet within Earth's liquid core has been discovered, providing new clues about the dynamics of our planet's magnetic field.

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School-Based Mindfulness Programs May Boost Kids' Mental Health

Drugs.com

FRIDAY, August 30, 2024 — Teaching schoolkids to practice mindfulness can boost their mental health — and, maybe, even their grades.That's the takeaway from a new review of more than three dozen research studies on school-based mindfulness int.

Research 105
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How Machine Learning Drives Clinical Trial Efficiency

Clinical trial data management is increasingly challenging as studies grow in complexity. Quickly accessing and analyzing study data is vital for assessing trial progress and patient safety. In this paper, we explore real-time data access and analysis for proactive study management. We investigate using adverse event (AE) data to monitor safety and discuss a clinical analytics platform that supports collaboration and data review workflows.

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Full study data back Alnylam heart drug’s benefit, but leave doctors with tough choices

BioPharma Drive: Drug Pricing

Detailed results from the Helios-B study support summary findings disclosed in June. But they may not make vutrisiran the standard of care as easily as Alnylam hopes.

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New Medical Technology Lights Up Bacteria Hiding in Wounds

Drugs.com

FRIDAY, Aug. 30, 2024 -- Fluorescent light can be used to highlight bacteria that hides in wounds, causing infections and slowing down the healing process, a new evidence review says.A handheld fluorescent device can light up bacteria in 9 out of.

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Novo builds heart failure case for semaglutide; Ventyx CFO departs

BioPharma Drive: Drug Pricing

A new analysis showed semaglutide reduced the risk of worsening heart failure. Elsewhere, the FDA approved a vaccine for mpox and a biotech planned layoffs.

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Traveling With a Loved One With Alzheimer's This Long Weekend? Experts Have Tips

Drugs.com

FRIDAY, Aug. 30, 2024 -- People can create many special moments if they include a loved one with dementia in their end-of-summer Labor Day getaway.However, they’ll need to take some special steps to make traveling as smooth as possible, according t.

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Deliver Fast, Flexible Clinical Trial Insights with Spotfire

Clinical research has entered a new era, one that requires real-time analytics and visualization to allow trial leaders to work collaboratively and to develop, at the click of a mouse, deep insights that enable proactive study management. Learn how Revvity Signals helps drug developers deliver clinical trial data insights in real-time using a fast and flexible data and analytics platform to empower data-driven decision-making.

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Fierce Biotech Editor-in-Chief Ayla Ellison Talks Shop with Michelle Benz on the Future of Biotech.

Fierce BioTech

Let's dive into a conversation with Ayla Ellison, Fierce Biotech Editor-in-Chief and Michelle Benz as they discuss the highlights and excitement surrounding this year's Fierce Biotech Summit. | Join Fierce Biotech Editors at Fierce Biotech Summit on Sept. 30-Oct.1 in Boston to learn, connect, and innovate with your industry peers.

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Billions of the World's People Deficient in Essential Micronutrients

Drugs.com

FRIDAY, Aug. 30, 2024 -- More than half of people around the world aren’t getting enough micronutrients essential to human health, including calcium, iron and vitamins C and E, a new study says.These deficiencies are contributing to global m.

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Women in STEM with Nadine Sprangers

Drug Target Review

Can you tell me more about your journey in the field of STEM and the challenges you encountered along the way? I started by studying pharmaceutical sciences with the initial plan of becoming a pharmacist and owning my own pharmacy. However, I pursued an additional year in industrial pharmacy, where I learned a lot about manufacturing and drug development, which I found really fascinating.

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Rural Hospitals Especially Vulnerable to Ransomware Attacks

Drugs.com

FRIDAY, Aug. 30, 2024 -- Rural hospitals – and their patients -- are particularly vulnerable to the aftershocks caused by ransomware attacks, a new study reports.“Ransomware attacks are bad news for hospitals and patients no matter where they hap.

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Clinical Data Like You´ve Never Seen It Before: Why Spotfire Is the Leading Tool for Clinical Analytics

Clinical development organizations face a wide array of challenges when it comes to data, many of which can impact the operational effectiveness of their clinical trials. In this whitepaper, experts from Revvity Signals explore how solutions like TIBCO® Spotfire® enable better, more streamlined studies. The whitepaper also features a success story from Ambrx, a leading biopharmaceutical company, detailing how it has leveraged Spotfire to tackle data quality and collaboration challenges in clinic

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How We Used Singlicate Analysis to Optimize Resource Utilization

Alta Sciences

How We Used Singlicate Analysis to Optimize Resource Utilization blussier Fri, 08/30/2024 - 14:51 HTML Achieving Efficiency and Cost Savings in Drug Development In the fast-paced world of drug development, where every sample counts, finding ways to optimize resources and accelerate results is critical. In this poster presentation, we discuss singlicate analysis, an innovative approach that focuses on individual samples to streamline processes.

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FDA AdComm to discuss patient-centric informed consent

Agency IQ

By Laura DiAngelo, MPH The FDA’s Center for Devices and Radiological Health (CDRH) will soon convene its Patient Engagement Advisory Committee to discuss “patient-centered informed consent” policies – notably, not just for medical devices but for “FDA regulated medical products” writ large. The meeting, scheduled for October 2024, will seek input and recommendations from the committee on the process for informed consent, “new areas of focus” for informed consent, and recent policy on “key inform

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Increasing Threat of Cyberattacks is Causing Energy Companies to Bolster Security

Perficient: Drug Development

A major energy and utilities supplier has become the latest victim in a growing list of organizations targeted by cyberattacks. Without a quick response to an attack like this, energy companies can risk exposing customer data, cutting off energy supply, slowing or completely stopping operations, and more. According to the Department of Energy, the recent incident was responded to quickly, and had minimal lasting impact.

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What we expect European regulators to do in September 2024

Agency IQ

By Sebastian Godoy, MPH , Corey Jaseph, MS, RAC , Kari Oakes In this recurring feature, AgencyIQ, through public data and previous analysis, determines what European medicine and device regulators will likely do in the month ahead, including key deadlines, meetings, events, planned regulations and comment periods. Fill out the form to read the full article.

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NET Core Renderings for XM Cloud finally gets some love

Perficient: Drug Development

That is not a secret – Sitecore always used to prioritize Next.Js framework as the first-class citizen for XM Cloud. All the best and finest features tend to find their way to a given framework in the first place. However, recently, there has been much activity around the. NET Core Rendering Framework which makes a lot of sense given most of us, Sitecore tech professionals, originate from the Microsoft and.NET background.

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An introduction to EU chemicals guidance

Agency IQ

By Scott Stephens, MPA In the internet age, meeting regulatory obligations starts with knowing where to pinpoint the right resources in the vast ocean of information to guide you successfully through the often-labyrinthine processes of EU chemicals regulation. he good news: ECHA offers a treasure trove of online guidance on Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), Classification, Labelling and Packaging (CLP), and other chemicals legislation, as well as other

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Lightning Talks

Broad Institute

Lightning Talks By lcopelan@broadinstitute.

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FDA finalizes inaugural guidance allowing certain device makers to submit quarterly malfunction reports

Agency IQ

By Laura DiAngelo, MPH Seven years after its inception, the FDA has finalized its first guidance on the Voluntary Malfunction Summary Report (VMSR) program for medical devices. While industry groups had asked for some additional flexibility and clarity in response to the draft version of the document, the agency largely finalized the document in alignment with that 2022 draft.

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What we expect EU chemical regulators to do in September 2024

Agency IQ

By Scott Stephens, MPA Welcome to AgencyIQ’s monthly roundup of EU chemical sector activities. This recurring feature compiles information from across EU agencies and institutions to deliver an overview of chemicals-related regulatory actions likely to happen in the month ahead, including planned legislation, consultations, webinars and meetings. Fill out the form to read the full article.

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Article FDA Thank You FDA AdComm to discuss patient-centric informed consent

Agency IQ

FDA AdComm to discuss patient-centric informed consent The FDA’s Center for Devices and Radiological Health (CDRH) will soon convene its Patient Engagement Advisory Committee to discuss “patient-centered informed consent” policies – notably, not just for medical devices but for “FDA regulated medical products” writ large. The meeting, scheduled for October 2024, will seek input and recommendations from the committee on the process for informed consent, “new areas of focus” for informed consent,

FDA 40
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Article Periodic Thank You An introduction to EU chemicals guidance

Agency IQ

An introduction to EU chemicals guidance In the internet age, meeting regulatory obligations starts with knowing where to pinpoint the right resources in the vast ocean of information to guide you successfully through the often-labyrinthine processes of EU chemicals regulation. The good news: ECHA offers a treasure trove of online guidance on Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), Classification, Labelling and Packaging (CLP), and other chemicals legislatio

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Analysis Life Sciences Thank You FDA finalizes inaugural guidance allowing certain device makers to submit quarterly malfunction reports

Agency IQ

FDA finalizes inaugural guidance allowing certain device makers to submit quarterly malfunction reports Seven years after its inception, the FDA has finalized its first guidance on the Voluntary Malfunction Summary Report (VMSR) program for medical devices. While industry groups had asked for some additional flexibility and clarity in response to the draft version of the document, the agency largely finalized the document in alignment with that 2022 draft.

FDA 40
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Analysis Chemical Thank You What we expect EU chemical regulators to do in September 2024

Agency IQ

What we expect EU chemical regulators to do in September 2024 Welcome to AgencyIQ’s monthly roundup of EU chemical sector activities. This recurring feature compiles information from across EU agencies and institutions to deliver an overview of chemicals-related regulatory actions likely to happen in the month ahead, including planned legislation, consultations, webinars and meetings.