Explore our blogs on various markets
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Health Equity in Pharma: Why It Matters and How to Act?
Health equity means everyone gets the care they need to live a healthy life. It means care and medicines reach people no matter their race, age, money, or where they live.. Right now, many people do not get fair care...
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Future of Pharma Demand: Forecasting Models Explained
Accurate drug demand forecasting is the key to keeping medicines available and avoiding waste. It helps companies plan production, manage supply chains, and meet patient needs on time.. The future of drug demand is shaped by many factors, such as aging populations, new diseases, patent expiries, and personalized medicine...
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Beyond Air Seeks FDA Nod for Next-Gen LungFit PH II
Beyond Air, Inc. (NASDAQ: XAIR) has submitted a premarket approval (PMA) supplement to the U.S. Food and Drug Administration (FDA) for its second-generation LungFit PH II system....
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FDA Approves First Treatment for Non-Cystic Fibrosis Bronchiectasis
The U.S. Food and Drug Administration (FDA) has approved BRINSUPRI™ (brensocatib), making it the first and only therapy for non-cystic fibrosis bronchiectasis (NCFB). . This chronic lung disease affects more than 500,000 people in the United States and has long been without an approved treatment option....
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4 Launch Strategies for Cell and Gene Therapies
Cell and gene therapies (CGTs) represent a new frontier in healthcare. These treatments aim to modify or replace cells and genes to treat or cure diseases that were previously untreatable. . While their promise is enormous, launching them is not simple...
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CRO Outsourcing Models for US Oncology Trials
Running oncology clinical trials in the US is complex and resource-heavy. Patient recruitment, biomarker testing, data collection, and regulatory reporting all demand specialized expertise. Pharmaceutical companies and biotech sponsors often rely on Contract Research Organizations (CROs) to manage parts or all of the trial process....
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Global Pharma Regulations 2025: Key Trends Shaping Strategy
Regulation shapes every part of the pharmaceutical industry. Agencies like the WHO, FDA (US), EMA (EU), MHRA (UK), ANVISA (Brazil), NMPA (China), and CDSCO (India) control how drugs are researched, developed, manufactured, and approved.. In 2025, these authorities are updating their frameworks to keep pace with artificial intelligence, digital health, advanced clinical trial models, sustainability rules, and global supply chain standards....
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Behavioural Science in Pharma Marketing (Explained)
Pharma companies spend billions every year trying to influence doctors, patients, and healthcare systems. Yet clinical data and product claims alone often fail to change outcomes. People rely on habits, emotions, social cues, and mental shortcuts, not just logic. ...
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Vaccine Market Entry: Regulations and Future Outlook
Vaccines are biological products that protect people from infectious diseases by stimulating the body’s immune system. They are one of the most effective tools in public health, reducing illness, saving lives, and lowering healthcare costs.. The demand for vaccines is increasing worldwide due to government immunization programs, new biotechnology platforms like mRNA, and a growing need to prevent both infectious and chronic diseases....
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Pharma R&D Efficiency: Metrics That Matter
Pharma R&D efficiency is under constant review by executives, investors, and regulators. The cost of bringing a new drug to market has increased, while success rates in clinical trials remain low. At the same time, pressure from pricing reforms, patent expiries, and investor expectations is forcing companies to do more with less....
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MaxCyte Launches Automation for Cell Therapy Manufacturing
Cell and gene therapies are changing modern medicine, offering new hope for patients with cancer, genetic disorders, and rare diseases. However, the success of these treatments depends on reliable and scalable manufacturing. Current processes are often complex, slow, and dependent on manual steps that introduce risks....
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Daré Bioscience & Rosy Wellness Launch Campaign for DARE to PLAY™
Daré Bioscience is set to launch DARE to PLAY™ Sildenafil Cream, the first evidence-backed topical treatment for female sexual arousal, in late 2025. Partnering with Rosy Wellness, the company has begun an awareness campaign to reduce stigma and provide women with trusted education and support around sexual health.. A Major Step Forward in Women’s Health...
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Global Pricing Trends For Generic Oncology Drugs
Cancer drugs remain among the most expensive medicines in healthcare. While innovative treatments bring hope, their high cost often restricts access for patients and strains health budgets. . Generic oncology drugs, both small-molecule generics and biosimilar,s have emerged as the most powerful tool to improve affordability. ...
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Galderma Begins Phase II Clinical Trials of Nemolizumab
Zug, Switzerland (June 26, 2025) – Galderma has announced two new Phase II clinical trials to study nemolizumab, a drug designed to block the IL-31 receptor. . These trials will focus on patients with Systemic Sclerosis (SSc) and Chronic Pruritus of Unknown Origin (CPUO), two conditions with high unmet medical needs and no approved treatments available.. What is Nemolizumab?...
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Roche Unveils Alzheimer’s Breakthroughs at AAIC 2025
Roche announced significant progress in its Alzheimer’s disease research portfolio during the Alzheimer’s Association International Conference (AAIC) 2025 in Toronto.. The company presented detailed results from its investigational therapy trontinemab and showcased its Elecsys pTau217 blood test, both of which aim to transform the detection and treatment of Alzheimer’s disease.. Advancing trontinemab with Brainshuttle technology...
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Cipla's Strategic Push into Global Respiratory Markets with Generic Advair
Cipla Limited has taken significant strides in its respiratory segment with the planned FY26 launch of its generic version of GlaxoSmithKline’s blockbuster asthma and COPD drug, Advair Diskus®, in the United States. . The move follows the successful completion of Phase-3 clinical trials and the filing of an Abbreviated New Drug Application (ANDA) with the US Food and Drug Administration (USFDA).. The Advair Opportunity: A Multi-Billion Dollar Market...
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10 Important Vaccine Market Trends of 2025
The global vaccine market is changing faster than ever, but many businesses, researchers, and policymakers struggle to keep up with the latest shifts.. Ignoring these changes can mean missed opportunities in investment, technology adoption, and public health preparedness. Falling behind could also leave gaps in vaccine access, innovation, and disease prevention....
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Patient Segmentation: Types and Strategies in Cardiology
Patient segmentation in cardiology helps hospitals and clinics group patients based on health risks, behavior, and outcomes.. This allows care teams to provide better, faster, and more personalized treatment.. With the rise of chronic heart diseases and growing data from EHRs and diagnostic tools, segmentation is now more important than ever....
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Aclaris Starts Phase 2 Trial of Bosakitug for Eczema
WAYNE, Pa. (June 2, 2025) — Aclaris Therapeutics, Inc. (NASDAQ: ACRS), a clinical-stage biopharmaceutical company focused on developing treatments for immuno-inflammatory diseases, has announced the initiation of a Phase 2 clinical trial of its leading drug candidate, bosakitug (ATI-045)....
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EU Endorses Camurus’ Oczyesa for Acromegaly Treatment
Lund, Sweden - April 25, 2025: Camurus has announced a major regulatory milestone as the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) issued a positive opinion for Oczyesa (CAM2029). This once-monthly treatment is designed for adult patients living with acromegaly, a rare hormonal disorder.. The recommendation is based on strong results from seven clinical trials, including two pivotal Phase 3 studies...