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What FDA’s “Healthy” Rule and Front-of-Pack Labelling Mean for Food Makers
Two changes are reshaping what goes on the front of a US food package. The first, a new definition of the "healthy" nutrient content claim, is already law, with enforcement starting on 25 February 2028 [1]. The second, mandatory front-of-pack labelling in the form of...
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Digital Health and the Reordering of Life Sciences Commercialization
It’s been an extraordinary two years for anyone working in pharma commercialization, with the macro environment shifting meaningfully under the feet of all those sitting on the commercial side of pharma or building in digital health with pharma partnership...
From Data to Decisions: The Next Frontier in Diabetic Foot Care
If you are not aware of the statistics on diabetic limb loss, they deserve your attention. Prevention is an absolute necessity. We call this diabetic foot care, and the way podiatrists utilize these opportunities is moving into a more data-rich era. Remote...
Expedited IND Pilot Opens as UK Fast Track Bars First-in-Human
The US Food and Drug Administration began accepting applications on 15 September 2026 for its expedited IND pilot. The programme is a key component of Operation TrialBlazer, according to the agency. The Department of Health and Human Services announced that initiative...
Why Pharmaceutical Quality Cannot Be Tested Into a Product
In pharmaceutical manufacturing, quality control testing is often the point at which a product gets its final analytical assessment. But from my experience in pharmaceutical quality control, one principle is worth emphasizing: QC testing is essential, but QC testing...
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Weekly News Roundup | 18 May 2026
Life science news 18 May 2026: FDA leadership turmoil, a landmark Alzheimer's breakthrough and a $15 billion China licensing deal define a historic week for the global industry. The week of 10 to 17 May 2026 delivered a concentration of high-impact events across...
Biologics on the Brink: The Patent Cliff Facing Big Pharma
The global pharmaceutical industry is approaching what many analysts are calling the largest patent cliff biologics in its history. This pharma patent cliff biologics analysts have long anticipated is now arriving in force. Between 2025 and 2030, drugs collectively...
Clinical Trials Roundup | 15 May 2026
AstraZeneca's eneboparatide meets the Phase 3 CALYPSO primary endpoint in chronic hypoparathyroidism with full data presented at the European Congress of Endocrinology, Alkermes' LUMRYZ meets its primary endpoint in the Phase 3 REVITALYZ trial for idiopathic...
GLP-1 Receptor Agonists Explained: How They Work and Who They’re For
Originally published 15 May 2026. Updated 28 June 2026 to reflect the latest approved indications, pipeline data, and access developments. GLP-1 receptor agonists have moved from specialist diabetes clinics to mainstream medicine with remarkable speed. Once known...
Hallmarks of Ageing as a Framework: How the Research Field is Evolving
When López-Otín and colleagues published “The Hallmarks of Aging” in Cell in 2013, they did something the field of biogerontology had quietly needed for decades: they created a framework. Nine interconnected processes, from genomic instability and telomere attrition...
Biotech M&A 2026: Every $1B+ Deal so Far and What is Driving Them
Updated 21 October 2026. First published 14 May 2026. Deal values and statuses are as of 21 October 2026. Biopharma M&A 2026 has already outrun last year. J.P. Morgan counts $138.9 billion of upfront M&A across 113 deals by the end of September. That is above...
Muscular Dystrophy Has New Treatments. Patients Still Can’t Get Diagnosed
A generation of transformative therapies is arriving for Duchenne muscular dystrophy. Gene therapies have reached the clinic. Oral small molecules targeting the fundamental biology of the disease are entering clinical trials. Newborn screening programmes are being...
Beyond GLP-1: The Future of Obesity Care is Hybrid
The emergence of GLP-1 receptor agonists has fundamentally reshaped obesity treatment. For the first time, we are seeing consistent, clinically meaningful weight loss at scale, supported by robust clinical programs such as STEP and SURMOUNT (Wilding et al., 2021;...
Using AI to Translate Fragmented Evidence into Formulation Logic
Thesis Early-stage life science development is increasingly constrained not by lack of data, but by fragmented, multi-scale evidence that resists straightforward interpretation. AI systems can assist in structuring this complexity – through literature triage,...
First Alzheimer’s Biomarker Reversal Linked to Lyme Disease Treatment
Alzheimer’s disease (AD) represents a significant medical concern for all of us as we grow older, as the NIH has published that the average risk of dementia over 55 years old is now 42%. AD is presently affecting 6.9 million Americans aged 65 or older and is expected...
Invisible Architect: How Infrastructure Drives Life Sciences Growth
In the high-stakes world of drug discovery and biomanufacturing, the spotlight typically shines on breakthrough modalities, venture rounds, and FDA milestones. Yet, behind every clinical success is a physical environment that either accelerated the science or quietly...
CagriSema: The Next Big Obesity Drug? What the Phase 3 Data Shows
The global obesity drug market is in the midst of its most competitive period in a generation. Since the approval of semaglutide as Wegovy and tirzepatide as Zepbound, pharmaceutical companies and investors have been watching closely for the next therapy capable of...
Weekly News Roundup | 18 May 2026
Life science news 18 May 2026: FDA leadership turmoil, a landmark Alzheimer's breakthrough and a $15 billion China licensing deal define a historic week for the global industry. The week of 10 to 17 May 2026 delivered a concentration of high-impact events across...
Biologics on the Brink: The Patent Cliff Facing Big Pharma
The global pharmaceutical industry is approaching what many analysts are calling the largest patent cliff biologics in its history. This pharma patent cliff biologics analysts have long anticipated is now arriving in force. Between 2025 and 2030, drugs collectively...
Clinical Trials Roundup | 15 May 2026
AstraZeneca's eneboparatide meets the Phase 3 CALYPSO primary endpoint in chronic hypoparathyroidism with full data presented at the European Congress of Endocrinology, Alkermes' LUMRYZ meets its primary endpoint in the Phase 3 REVITALYZ trial for idiopathic...
GLP-1 Receptor Agonists Explained: How They Work and Who They’re For
Originally published 15 May 2026. Updated 28 June 2026 to reflect the latest approved indications, pipeline data, and access developments. GLP-1 receptor agonists have moved from specialist diabetes clinics to mainstream medicine with remarkable speed. Once known...
Hallmarks of Ageing as a Framework: How the Research Field is Evolving
When López-Otín and colleagues published “The Hallmarks of Aging” in Cell in 2013, they did something the field of biogerontology had quietly needed for decades: they created a framework. Nine interconnected processes, from genomic instability and telomere attrition...
Biotech M&A 2026: Every $1B+ Deal so Far and What is Driving Them
Updated 21 October 2026. First published 14 May 2026. Deal values and statuses are as of 21 October 2026. Biopharma M&A 2026 has already outrun last year. J.P. Morgan counts $138.9 billion of upfront M&A across 113 deals by the end of September. That is above...
Muscular Dystrophy Has New Treatments. Patients Still Can’t Get Diagnosed
A generation of transformative therapies is arriving for Duchenne muscular dystrophy. Gene therapies have reached the clinic. Oral small molecules targeting the fundamental biology of the disease are entering clinical trials. Newborn screening programmes are being...
Beyond GLP-1: The Future of Obesity Care is Hybrid
The emergence of GLP-1 receptor agonists has fundamentally reshaped obesity treatment. For the first time, we are seeing consistent, clinically meaningful weight loss at scale, supported by robust clinical programs such as STEP and SURMOUNT (Wilding et al., 2021;...
Using AI to Translate Fragmented Evidence into Formulation Logic
Thesis Early-stage life science development is increasingly constrained not by lack of data, but by fragmented, multi-scale evidence that resists straightforward interpretation. AI systems can assist in structuring this complexity – through literature triage,...
First Alzheimer’s Biomarker Reversal Linked to Lyme Disease Treatment
Alzheimer’s disease (AD) represents a significant medical concern for all of us as we grow older, as the NIH has published that the average risk of dementia over 55 years old is now 42%. AD is presently affecting 6.9 million Americans aged 65 or older and is expected...
Invisible Architect: How Infrastructure Drives Life Sciences Growth
In the high-stakes world of drug discovery and biomanufacturing, the spotlight typically shines on breakthrough modalities, venture rounds, and FDA milestones. Yet, behind every clinical success is a physical environment that either accelerated the science or quietly...
CagriSema: The Next Big Obesity Drug? What the Phase 3 Data Shows
The global obesity drug market is in the midst of its most competitive period in a generation. Since the approval of semaglutide as Wegovy and tirzepatide as Zepbound, pharmaceutical companies and investors have been watching closely for the next therapy capable of...
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Weekly News Roundup | 11 May 2026
Life science news 11 May 2026: M&A momentum, artificial intelligence diagnostics and a record week for deal-making define an active seven days for the global life science industry. The week of 4 to 10 May 2026 produced a dense cluster of major acquisitions, a...
Why “Hot” Therapeutic Areas Break Traditional Benchmarks
In fast-moving areas like radiopharmaceuticals and precision immunology, the biggest portfolio risk is often not uncertainty itself, but false certainty created by mismatched benchmarks. As life sciences enters a more disciplined cycle, one pattern shows up across...
Is Photodisinfection the New Alternative to Traditional Antibiotics?
Few ideas in modern medicine are as unsettling as the prospect of a “post-antibiotic era.” For decades, antibiotics have underpinned infection control, transforming once-lethal diseases into manageable conditions. Yet their effectiveness is steadily eroding....
Orforglipron Approved: Inside the Oral GLP-1 Race
The obesity treatment landscape shifted decisively on 1 April 2026, when the US Food and Drug Administration approved Foundayo (orforglipron), an oral once-daily glucagon-like peptide-1 (GLP-1) receptor agonist developed by Eli Lilly. The decision marks the arrival of...
Clinical Trials Roundup | 8 May 2026
Cytokinetics’ aficamten meets dual primary endpoints in the pivotal Phase 3 ACACIA-HCM trial for non-obstructive hypertrophic cardiomyopathy, Axsome Therapeutics secures FDA approval of AUVELITY as the first non-antipsychotic treatment for Alzheimer’s disease...
GSK Secures $1bn Rights to SiranBio siRNA Therapy
GSK has entered into an exclusive licensing agreement with Chinese biotech Suzhou Siran Biotechnology (SiranBio), securing global rights to the company's early-stage small interfering RNA (siRNA) therapy, SA030, in a deal worth up to $1.005 billion in potential...
From Wrist to Ward: Which Wearables Have Earned Clinical Trust
The wearable health technology market has expanded at a pace that regulators, clinicians, and patients have struggled to keep up with. Smartwatches, adhesive biosensors, continuous glucose monitors, and cardiac patches are now part of the fabric of daily life for...
Why Innovation in Oncology Diagnostics Is An Imperative We Must Prioritize
Not long ago, I spoke with a colleague, a mother named Kelley who has spent the past two years asking a question that increasingly reflects a broader challenge in oncology: If technologies exist to detect cancer earlier, why aren’t we dedicating more effort to support...
India, Brazil and Southeast Asia: The New Pharma Powerhouses
For most of the twentieth century, the global pharmaceutical industry operated on a straightforward geographic logic. Drugs were discovered and developed in North America and Western Europe, approved by the FDA and EMA, and then exported to the rest of the world. The...
Paediatric Trials: Why Children Remain Therapeutic Orphans
Children have long been described as therapeutic orphans. It is a term first used by the American paediatrician Harry Shirkey of the Children’s Hospital in Birmingham, Alabama, at a 1963 conference and formally published in 1968. Despite more than five decades of...
Global Nursing Shortage: The Life Sciences Risk
For the life sciences sector, the global nursing shortage is not a background public health concern. It is a clinical trial staffing problem, a pharmaceutical market access problem, and a real-world evidence problem. The WHO's 2025 State of the World's Nursing report...
Why Clinical Trial Diversity Remains a Problem
For decades, clinical trials have failed to adequately represent the patients who will ultimately use the medicines and treatments being tested. Gaps in enrolment across race, ethnicity, sex, age, and socioeconomic background have created an incomplete evidence base,...
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LifeScienceDaily.news is building a new kind of platform where innovators, researchers, and industry leaders tell their own stories and shape the narrative of what’s next in life sciences. Share your story and lead the conversation.
Don’t wait for the media to pick up your story. Be the media.
See More Articles
Want to Be Part of the Next Chapter in Life Sciences Media?
LifeScienceDaily.news is building a new kind of platform where innovators, researchers, and industry leaders tell their own stories and shape the narrative of what’s next in life sciences. Share your story and lead the conversation.