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Dentsply Sirona, FDI, and Smile Train Expand Digital Cleft Care Education to Reach More Providers Worldwide

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SHERIDAN, WYOMING – August 26, 2025 – Dentsply Sirona, the FDI World Dental Federation (FDI), and Smile Train have expanded their joint cleft care education program, introducing multilingual access to their digital training platform and new workflow videos aimed at improving cleft treatment globally. The initiative, timed with Cleft Awareness Month, underscores a strategic push to equip dental professionals with advanced tools, protocols, and training to address one of the most common congenital conditions affecting children worldwide.

Expanding Global Reach Through Multilingual Training

ECR Tag 2025: AI, Collaboration, and Consumer Insights Set to Reshape Retail Strategies

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SHERIDAN, WYOMING – August 26, 2025 – The ECR Tag 2025 in Cologne is set to bring together leaders from retail, consumer goods, and technology for two days of strategy-focused exchange, highlighting how AI, collaboration, and consumer-centric innovation are redefining competitive growth models in the sector.

AI-Driven Retail Transformation on the Agenda
Artificial intelligence will be a central theme at this year’s event, with executives from Amazon Web Services outlining how AI agents are reshaping category management and retail operations. The focus extends beyond automation, emphasizing decision intelligence, real-time personalization, and supply chain optimization as key levers for retailers adapting to shifting consumer expectations.

GS1 and Meta to Showcase AI-Powered Retail Innovation at 2025 Summit in Cologne

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SHERIDAN, WYOMING – August 26, 2025 – GS1 Germany and Meta are set to co-host the Retail Summit 2025 on November 5 in Cologne, bringing together leading retailers, technology providers, and brand executives to explore how artificial intelligence, retail media, and immersive experiences are reshaping commerce across Europe. Under the theme “Where Technology Meets Experience,” the event aims to highlight best practices from both established brands and Silicon Valley innovators.

A Platform for Retail AI and Emerging Technologies

Zukunft Personal Europe 2025: 25 Years of HR Innovation and a New Era for People & Organizational Performance

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SHERIDAN, WYOMING – August 26, 2025 – Zukunft Personal Europe (ZP Europe) is set to mark its 25th anniversary with a forward-looking edition in Cologne from September 9–11, 2025. Positioned under the theme “Time for New Beginnings”, the event will move beyond retrospectives to highlight transformation strategies, cutting-edge HR technology, and organizational models for a rapidly evolving workplace.

From HR Fair to European Transformation Hub

Once launched as a specialized HR trade fair, Zukunft Personal has evolved into Europe’s leading platform for people and organizational performance. In 2025, the anniversary event aims to showcase how businesses can address interconnected challenges in leadership, digitalization, workplace culture, and resilience. Organizers emphasize that the focus is no longer just human resources, but broader structural change shaping enterprises across industries.

Oral Obesity Drug Pipeline Heats Up as Competitors Eye Eli Lilly’s Market Lead

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SHERIDAN, WYOMING – August 12, 2025 – Eli Lilly’s Phase III results for its next-generation oral GLP-1 therapy, orforglipron, have energized the already competitive obesity drug market, sparking renewed focus on oral weight-loss candidates poised to challenge the injectable-dominated landscape. While Lilly’s data confirmed significant efficacy, industry analysts see room for competitors to gain ground with differentiated mechanisms, dosing advantages, and manufacturing scalability.

The ATTAIN-1 study showed orforglipron achieved an average 12.4% weight reduction over 72 weeks, compared with 0.9% for placebo, with nearly 60% of high-dose patients losing at least 10% of body weight. However, analysts at Truist Securities and William Blair noted the therapy’s performance fell short of expectations set by leading injectable GLP-1 agonists—creating an opening for rivals.

Market Shift Toward Oral Obesity Therapies

AAV Gene Therapy Faces Safety Scrutiny Amid Sarepta-Linked Patient Deaths — Industry Considers Next Steps

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SHERIDAN, WYOMING – August 12, 2025 – A wave of safety concerns surrounding adeno-associated virus (AAV) gene therapy has hit the biotechnology sector following multiple patient deaths linked to Sarepta Therapeutics’ platform. While some stakeholders push for urgent refinements to the decades-old technology, others are accelerating work on alternative delivery systems that could reshape the future of genetic medicine.

HHS Leadership Shake-Up Follows Controversial mRNA Contract Cancellations

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SHERIDAN, WYOMING – August 12, 2025 – The Department of Health and Human Services (HHS) is facing fresh turbulence after the abrupt dismissal of Gray Delany, the lead implementor of the Make America Healthy Again (MAHA) initiative. The move comes just days after Health Secretary Robert F. Kennedy Jr. terminated 22 mRNA vaccine contracts worth a combined $500 million, triggering intense debate across the biomedical and public health sectors.

FDA Narrows Skysona Access as Post-Marketing Data Shows Elevated Cancer Risk

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SHERIDAN, WYOMING – August 12, 2025 – The U.S. Food and Drug Administration (FDA) has significantly tightened prescribing criteria for bluebird bio’s Skysona, an autologous hematopoietic stem cell-based gene therapy for cerebral adrenoleukodystrophy (CALD). The treatment is now limited to patients with no other therapeutic options or available stem cell donors, following post-marketing findings of a substantially higher incidence of hematologic malignancies than previously reported.

mRNA Immunotherapy: Industry Urged to Step Up as Federal Cuts Threaten Cancer Breakthroughs

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SHERIDAN, WYOMING – August 11, 2025 – The U.S. pharmaceutical sector faces a pivotal moment as recent federal funding cuts to mRNA vaccine programs threaten to slow one of oncology’s most promising frontiers: dendritic cell–based mRNA cancer immunotherapies. With the Department of Health and Human Services ending approximately $500 million in BARDA contracts, industry stakeholders are being called upon to bridge the gap and accelerate clinical translation.

Why mRNA Technology Is Critical for Cancer Immunotherapy

Boehringer Ingelheim Enters Oncology Market With FDA Approval of Hernexeos for HER2-Mutant NSCLC

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SHERIDAN, WYOMING – August 11, 2025 – Boehringer Ingelheim has secured FDA accelerated approval for its kinase inhibitor Hernexeos (zongertinib), marking the German pharmaceutical company’s first entry into the oncology market in its 140-year history. The approval positions Hernexeos as a new targeted therapy for adult patients with unresectable or metastatic non-small cell lung cancer (NSCLC) harboring HER2 tyrosine kinase domain (TKD)–activating mutations.

Targeted Innovation in HER2-Mutant NSCLC
Hernexeos is designed as an oral, selective, and irreversible HER2 inhibitor that disrupts cell growth and division driven by HER2 signaling. By directly addressing this oncogenic pathway, the drug aims to provide a new treatment option for a patient subset that historically faces poor prognoses and limited targeted therapy choices.

Midea Group to Showcase Human-Centric Appliance Innovation at IFA 2025 with Küppersbusch, Teka, and Eureka

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SHERIDAN, WYOMING – August 10, 2025 – Midea Group will make a significant statement at this year’s IFA trade fair, occupying an expansive 2,600-square-meter exhibition space in Hall 5.1. The showcase will feature a diverse portfolio of home appliance and air conditioning solutions, with first-time participation from Küppersbusch Hausgeräte GmbH and its premium brands Küppersbusch and Teka, alongside U.S.-based vacuum cleaner specialist Eureka.

A Unified Platform for Global Brand Visibility

Under the overarching theme “Humanizing Technology,” Midea Group aims to highlight product innovations designed around user experience, energy efficiency, and lifestyle integration. For Küppersbusch and Teka, the event marks a strategic entry onto the IFA stage, allowing these European brands to strengthen their market positioning through direct engagement with international distributors, retailers, and technology partners.

MWC Barcelona 2026 to Mark 20 Years of Global Connectivity Leadership

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SHERIDAN, WYOMING – August 10, 2025 – The GSMA is preparing to host one of the most significant technology gatherings of the decade as MWC Barcelona returns March 2–5, 2026, celebrating 20 years of convening global connectivity leaders. The milestone event aims to blend two decades of innovation with a forward-looking agenda focused on AI, 5G, enterprise technology, and policy shaping for the next generation of connected solutions.

Two Decades of Industry Collaboration and Impact

Since its inception, MWC Barcelona has served as a strategic platform where network operators, device manufacturers, policymakers, and technology investors converge. The event’s legacy is rooted in driving advancements in global communications, from the earliest mobile broadband rollouts to the current surge in edge computing, private networks, and IoT integration.

Elevating the Global Stage in 2026

Eli Lilly Confronts Triple Pricing Pressures While Positioning for Long-Term Value in Competitive Obesity Drug Market

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SHERIDAN, WYOMING – August 10, 2025 – Eli Lilly is navigating a three-pronged challenge on drug pricing, from regulatory proposals to competitive market dynamics, even as it advances its next-generation oral weight loss candidate, orforglipron. On its second quarter earnings call, the company’s leadership underscored that pricing strategy will remain central to sustaining market share and delivering shareholder value.

Balancing Innovation and Pricing in Obesity Therapeutics

Lilly’s much-anticipated oral GLP-1 receptor agonist, orforglipron, is positioned to compete directly with Novo Nordisk’s blockbuster obesity portfolio. With the oral format offering improved patient convenience over injectable therapies, analysts expect robust uptake potential. However, the commercial rollout will hinge on a price point that supports payer coverage while defending against Most Favored Nation (MFN) pricing pressures at the federal level.

Globus Medical Delivers Record Q2 Profitability, Strengthens Spine Portfolio with Nevro Integration

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SHERIDAN, WYOMING – August 10, 2025 – Globus Medical, Inc. (NYSE: GMED) reported strong second-quarter 2025 results, achieving record non-GAAP earnings per share and double-digit revenue growth, driven by its U.S. Spine business and strategic integration of Nevro. The performance underscores the company’s operational discipline and its continued push to expand robotic-assisted surgery adoption.

Double-Digit Revenue Growth Across Core Segments

Worldwide net sales reached $745.3 million, an 18.4% year-over-year increase, or 17.6% on a constant currency basis. U.S. net sales rose 20.3%, while international revenue grew 11% as reported. The company’s Musculoskeletal Solutions segment generated $710.2 million, with Enabling Technologies contributing $35.2 million after a modest rebound in demand.

Operational Leverage and Profitability Milestones

Gilead Maintains Confidence in PrEP Franchise as U.S. Preventive Services Task Force Faces Uncertainty

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SHERIDAN, WYOMING – August 10, 2025 – Gilead Sciences is signaling strong confidence in its HIV prevention portfolio, including the twice-yearly injectable PrEP therapy Yeztugo, despite growing uncertainty over the future of the U.S. Preventive Services Task Force (USPSTF). The federally recognized panel’s recommendations currently mandate insurance coverage for preventive services, but a postponed meeting has fueled speculation that Health Secretary RFK Jr. could overhaul or dismantle the group.

Regulatory Shifts Could Reshape PrEP Access

The USPSTF plays a critical role in defining access to preventive medicines by issuing recommendations that directly influence payer coverage. For HIV prevention, its endorsement has helped accelerate adoption of both oral and long-acting injectable PrEP solutions. A structural change to the task force could:

Vinay Prasad Returns as CBER Director, Reinstating FDA Leadership Stability Amid Biologics Sector Uncertainty

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SHERIDAN, WYOMING – August 10, 2025 – In a rapid reversal, Dr. Vinay Prasad has resumed leadership of the U.S. Food and Drug Administration’s (FDA) Center for Biologics Evaluation and Research (CBER) less than two weeks after stepping down. The reinstatement, confirmed by the Department of Health and Human Services (HHS), ends speculation over the agency’s direction during a critical period for advanced biologics oversight.

FDA Leadership Transition Reverses Course

Prasad’s reinstatement follows his abrupt July 29 resignation, which had raised questions within regulatory, biotech, and patient advocacy circles. HHS spokesperson Andrew Nixon confirmed to STAT News that “At the FDA’s request, Dr. Vinay Prasad is resuming leadership of the Center for Biologics Evaluation and Research,” signaling a renewed alignment between CBER and the agency’s strategic objectives.

Sailor Foods Marks 30 Years with Strategic Brand, Product, and Channel Overhaul

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SHERIDAN, WYOMING – August 8, 2025 – Sailor Foods Co., Ltd., a long-established Chinese heritage food producer, has marked its 30th anniversary with a sweeping transformation plan that blends brand modernization, product innovation, and multi-channel market expansion. The company’s “Riding the Waves – Thirty Years and Leaping Ahead” customer appreciation event in Putian brought together nearly 1,000 industry partners, underscoring its ambitions to compete in both domestic and international markets over the next decade.

Brand Modernization to Align with New Consumer Era

Organic Spirulina Market Set to Surpass $500 Million by 2035 as Demand for Premium, Sustainable Nutrition Accelerates

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SHERIDAN, WYOMING – August 9, 2025 – The global organic spirulina market is entering a period of unprecedented growth, with revenues projected to rise from $140 million in 2025 to $515 million by 2035, according to industry forecasts. This expansion, at a compound annual growth rate (CAGR) of 13.5%, reflects a broader shift toward clean-label, certified-organic products in both nutraceutical and functional food sectors.

Cell and Gene Therapy at a Crossroads: Scaling Innovation for Commercial Viability

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SHERIDAN, WYOMING – August 9, 2025 – The cell and gene therapy (CGT) sector stands at a pivotal moment. Once buoyed by multibillion-dollar valuations, companies like Sarepta Therapeutics and bluebird bio have faced sharp declines, underscoring the sector’s commercial growing pains. Industry leaders now agree: sustainable success will depend on advancing manufacturing, aligning global regulations, and better communicating value to payers.

Next-Generation Manufacturing as a Growth Engine

Panelists at the recent BIO Convention in Boston pointed to decentralized, modular manufacturing as a critical enabler for CGT expansion. The U.K.’s Medicines and Healthcare products Regulatory Agency (MHRA) has taken the lead with formal guidelines for point-of-care production, a move welcomed by innovators like Ori Biotech CEO Jason Foster. In the U.S., the FDA has yet to implement a comparable framework.

Big Pharma’s Venture Arms and Incubators Target Next-Generation Drug Innovation

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SHERIDAN, WYOMING – August 8, 2025 – Major pharmaceutical companies are doubling down on venture funds and incubator programs to identify cutting-edge science, foster strategic partnerships, and position themselves in emerging therapeutic and geographic markets. While mergers and acquisitions remain a dominant growth driver, these initiatives provide a long-term “farm system” for high-value pipeline assets.

From Discovery Hubs to Strategic Pipelines
Eli Lilly’s Lilly Gateway Labs and Boehringer Ingelheim’s Venture Fund illustrate how Big Pharma is building innovation capacity beyond their core research programs. These initiatives target startups with disruptive science in neuroscience, oncology, immunology, and cardiometabolic health—while also venturing into high-risk areas such as neurodegenerative diseases and healthspan research.