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Sustainability has become central to the mission of hospital pharmacists, who are uniquely positioned to minimise waste, reduce healthcares environmental footprint and enhance patient outcomes. In his latest commentary, Dr Joo Gonalves PhD explores how digital health tools, artificial intelligence and circular economy models can drive meaningful change in hospital pharmacy practice.
New findings from The Pistoia Alliance report major challenges to adoption of data-driven innovation and AI in life sciences. The research is based on a poll conducted at the organisations annual European conference. Resistance to change emerged as the biggest obstacle to innovation (51 percent). To overcome this, the Alliance urged the pharmaceutical industry to prioritise cultural and behavioural change in digital transformation efforts.
Venlafaxine , commonly known by the brand name Effexor or Effexor XR, is a prescription drug used to manage symptoms of depression and other mood disorders. After being prescribed venlafaxine, you might wonder about your lifestyle choices while on this drug. A common question arises when people get invited to a social gathering or celebrationcan you enjoy a drink while taking venlafaxine?
If you think your patients arent looking at online pharmacies for cheaper medications, youre kidding yourself. Medicine is expensiveeverything is expensive. And when people are desperate, they look for alternatives. The problem? 96% of online pharmacies are illegal. Theyre selling unregulated, potentially dangerous medications, and most patients have no idea.
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
Introduction If the past few years have taught pharma marketers anything, it’s that agility, data, and digital-first thinking aren’t just buzzwordsthey’re survival tactics. Marketing in pharma has undergone a radical shift, propelled by digital transformation, patient-centric demands, and evolving regulatory landscapes. In 2025, the strategies that succeed are rooted in personalization, innovation, and real-time adaptability.
After Hurricane Ian, as Floridians returned home to sodden furniture and moldy piles of debris, many with asthma could feel their chests tightening. To figure out what was safe, some sent their concerns directly to the U.S. Centers for Disease Control and Prevention. But on Tuesday — days before floods ravaged Nashville, potentially prompting similar queries — the people who would normally answer such asthma questions stopped working.
Analytical testing is an essential part of guaranteeing the quality, safety and effectiveness of pharmaceutical products. However, the process is not without its challenges and it requires a proactive approach if both compliance and efficiency are to be maintained. This is why it is essential to develop and validate analytical methods to support activities and functions such as process validation controls, stability tests and dissolution profiles.
Analytical testing is an essential part of guaranteeing the quality, safety and effectiveness of pharmaceutical products. However, the process is not without its challenges and it requires a proactive approach if both compliance and efficiency are to be maintained. This is why it is essential to develop and validate analytical methods to support activities and functions such as process validation controls, stability tests and dissolution profiles.
Telemedicine is defined as the remote delivery of healthcare services using a phone, tablet, or computer, according to the Centers for Disease Control and Prevention. Starting with the COVID-19 pandemic, telemedicine expanded rapidly and redefined the delivery of medical services in virtually every aspect of healthcare. Pharmacy is no exception. Telepharmacy utilizes technology to deliver pharmacy services in an innovative way, according to an article published in Integrated Pharmacy Research an
In the world of pharma marketing, the strategies that truly resonate are often those rooted in trust. Thats why referral marketing is gaining traction among pharmaceutical brands looking to increase engagement with both healthcare professionals and patients. Rather than relying solely on paid ads or direct promotion, referral marketing uses personal recommendations to generate awareness, interest, and ultimately, conversions.
Hotlines that have fielded millions of calls from people — including new mothers — looking for mental health support or to quit smoking are in limbo after federal officials fired the workers who oversaw them. Employees were cut from offices that fund prevention work on the local, state, and tribal level. Those include hotlines like the Maternal Mental Health Hotline run by the Health Resources and Services Administration, and another to help smokers quit using tobacco.
A new toolkit to support pharmacists when integrating artificial intelligence (AI) into daily practice has been launched by the International Pharmaceutical Federation (FIP). The toolkit for hospital, industry and community settings offers structured guidance on AI adoption. It covers ethical considerations, implementation strategies, regulatory compliance and real-world applications to help pharmacists optimise patient care, stimulate multidisciplinary interaction and enhance operational effici
Access to limited distribution drugs and payer contracts are key to pharmacy expansion. But how do you prepare your operations to take the next step? Meaningful data: Collect and share clinical data regarding outcomes, utilization, and more Reporting: Limited distribution models require efficient tracking and reporting systems Workflows: Align workflows with specific pharma and payer contractual requirements For in-depth, expert insights on pharmacy expansion, watch this webinar from Inovalon.
Olanzapine (brand names Zyprexa or Zyprexa Zydis) is a second-generation antipsychotic medication that’s FDA approved to treat mental health conditions like schizophrenia and bipolar disorder, including mixed or manic episodes. It’s also approved for treatment-resistant depression or depression with bipolar I disorder in combination with fluoxetine.
Introduction Pharmaceutical marketing is entering a new era in 2025, driven by rapid advancements in technology, evolving patient expectations, and tighter compliance demands. As industry leaders adapt to digital-first communication and omnichannel engagement, the need for smart, scalable, and strategic marketing tactics is more urgent than ever. Whether you’re launching a new branded drug or optimizing an established portfolio, staying ahead of the curve in pharmaceutical marketing has be
Dana, a 29-year-old nurse in St. Louis, checks her phone to see if the gig nursing app CareRev still has her scheduled at the local hospital. She’s already arranged child care for her son, but cancellations are common. “It’s a gamble. … I’ll wake up at 5 in the morning, and I’ll find out if I’m canceled or not,” she told us.
A new progesterone-based treatment aimed at preventing miscarriage has been launched across the UK, following a major clinical trial that demonstrated a significant improvement in live birth rates. Prometrium, a 400mg soft vaginal capsule developed by Besins Healthcare, is now available in England, Wales, Scotland and Northern Ireland. It is designed for use by women […] The post New hormonal treatment launched to help prevent miscarriage in early pregnancy appeared first on Pharmafile.
Speaker: Dr. Ben Locwin - Biopharmaceutical Executive & Healthcare Futurist
What will the future hold for clinical research? A recent draft from the FDA provides valuable insight. In "Optimizing the Dosage of Human Prescription Drugs and Biological Products for the Treatment of Oncologic Diseases," the FDA notes that "targeted therapies demonstrate different dose-response relationships compared to cytotoxic chemotherapy, such that doses below the Maximum Tolerated Dose (MTD) may have similar efficacy to the MTD but with fewer toxicities.
Bonjesta is a brand-name prescription drug used to treat nausea and vomiting associated with pregnancy. This medication is an oral tablet that contains the medicines doxylamine and pyridoxine (a form of vitamin B6 ). Currently, there is not a generic version of Bonjesta. Managing nausea and vomiting during pregnancy is usually first controlled with diet and lifestyle adjustments.
The words fish oil invoke a particular disgust response in me every time I hear them. As a non-fish eater, I get annoyed by the onslaught of supposed health benefits of eating fish and/or taking fish oil supplements. I wanted to dive into whats good, whats bad, and if there are any options out there for those of us who may be vegetarian or dont eat fish.
Food has been front and center in the Make America Healthy Again movement, Health Secretary Robert F. Kennedy Jr.’s campaign to solve chronic disease in the United States. That’s why forthcoming federal guidance on nutrition could draw extra attention this time around, even as a massive reorganization of the nation’s health workforce unfolds.
Introduction How might your pharmaceutical marketing strategy change if your core products suddenly became more expensive to import or export? Pharma tariffs have quickly emerged as a critical consideration for pharma marketing executives, reshaping how brands strategize, position, and market their products globally. As the landscape evolves, marketers need clarity on navigating this complex terrain effectively.
Are you still using workarounds to manage your daily operations? To achieve peak performance, it's time to explore other options for specialty and infusion pharmacy software. Streamline pharmacy operations and improve clinical performance with automated processing, real-time data exchange, and electronic decision support. Download this helpful infographic to: Drive efficiency and patient adherence from referral receipt to delivery and ongoing care – all with our Pharmacy Cloud.
With the skyrocketing popularity of injectable medications Ozempic and Wegovy , a shortage inevitably followed. Ozempic and Wegovy (and Rybelsus , which is oral semaglutide) are GLP-1 receptor agonists (glucagon-like peptide-1 receptor agonists, commonly referred to as GLP-1s) and are the only FDA-approved drugs that contain the active ingredient semaglutide.
The US Food and Drug Administration (FDA) has approved Qfitlia (fitusiran) as the first therapy in the US to treat haemophilia A or B, with or without inhibitors. The approval of the antithrombin-lowering (AT) drug was based on data from the ATLAS phase 3 studies that Sanofi conducted. Sanofi is an international pharma and healthcare […] The post Qfitlia approved by FDA to treat haemophilia A or B appeared first on Pharmafile.
Layoff notices began arriving early Tuesday for thousands of employees of the sprawling Department of Health and Human Services and its subsidiary agencies, with as many 10,000 workers potentially expected to be hit by the cuts. “I regret to inform you that you have been affected by a reduction in force (RIF) action,” an email to affected employees said.
By Dr. Naomi Lowy, Principal Drug Regulatory Expert Trade and national press have reported that recent changes in FDA staffing levels have already led to slower responses to calls and emails. According to reports, which were published before the most recent reports of HHS staff level reductions and tumultuous changes in leadership, FDA staff were missing minor deadlines.
Ozempic is the brand name for semaglutide, which is a medication thats FDA approved to treat high blood sugar in people with Type 2 diabetes. It is also often prescribed off-label as a weight loss medication, even in patients with normal blood sugars. Ozempic is a type of medication called a glucagon-like peptide-1 agonist (GLP-1) and is only given by injection.
Mehilinen, a Finnish health and social care provider, has announced that it has agreed to acquire Regina Maria and MediGroup. In conjunction with these, Hellman & Friedman (H&F) joins CVC in an investment partnership in the company. These developments form part of Mehilinens international growth strategy which focuses on expanding both in Finland and in […] The post Mehilinen acquires Regina Maria and MediGroup, and welcomes Hellman & Friedman as new shareholder appeared first
As a longtime dog owner, I assumed that each bag of my dogs’ commercial pet food was closely monitored by the federal Food and Drug Administration (FDA). It turns out I was wrong. More than 102 million U.S. households own a dog or a cat, and thousands more have fish, birds, or reptiles. The resulting pet food industry is massive — Americans spent $65 billion on pet food and treats in 2023 alone.
As we settle into Spring celebrating our 150th year in business, theres been a big shake-up in the world of pharmacy. If you caught the news last month, you may have seen that Sycamore Partners, a private equity firm, is purchasing Walgreens. The same company that owns The Limited, Hot Topic, and Staples is now in charge of one of Americas largest drugstore chains.
Abilify (aripiprazole ) is a second-generation antipsychotic medicine used primarily in the treatment of bipolar disorder , schizophrenia , and depression. S econd-generation antipsychotics possess mood-stabilizing potential to go along with a lower risk of side effects than first-generation antipsychotics and an array of dosage forms. Efficacy, fewer adverse events, and convenience sound like an enticing trio of features, but Abilify may not be the best choice among the group.
ProBioGen has announced the appointment of Alfred Merz as its chief executive officer (CEO), effective 1 April 2025. Merz, who was previously chief operating officer (COO) and interim CEO, now assumes leadership of the company. Merz has over 30 years’ worth of experience in manufacturing, operations and strategy development. Before joining ProBioGen 2024, he was […] The post Alfred Merz appointed as CEO of ProBioGen appeared first on Pharmafile.
There’s a theory of cancer causation that I’ve been thinking about recently called the two-hit hypothesis. It proposes that cancer begins with two mutations: one that can be inherited and one that is influenced by environmental or other factors. Public health seems to be in the midst of experiencing two hits. The result could be deadly.
OctariusRx President and Consultant Pharmacist Victor Alves is presenting Pharmacy Documentation: Tips for Patient Safety and Survey Success at the ASCA 2025 Conference & Expo, April 30May 3, in Denver Colorado. He will discuss the essential elements of patient safety through complete pharmacy documentation. Additionally, he will address the most common survey issues and provide practical tips for improving patient safety and survey success.
Semaglutide (the active ingredient in brand-name drugs Ozempic , Rybelsus , and Wegovy ) is a GLP-1 receptor agonist , antidiabetic, and weight loss drug. The injectable medicine, Ozempic, is approved by the U.S. Food and Drug Administration (FDA) to treat Type 2 diabetes and lower the risk of cardiovascular events and kidney problems in certain adults.
Bristol Myers Squibb (BMS) has received a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) for its immunotherapy drug Opdivo (nivolumab), marking a major step towards expanding treatment options for patients with resectable non-small cell lung cancer (NSCLC) in the EU. CHMP, part of the European Medicines Agency (EMA), has recommended […] The post Bristol Myers Squibb receives positive CHMP opinion for Opdivo treatment appeared first on Pharmafile.
In a rare move, the Food and Drug Administration told an unspecified number of drug companies that studies used to support therapeutic equivalence of some of their medicines have been rejected due to false data generated by a contract research organization. The agency identified “significant” problems with data integrity and the way studies were conducted by Raptim Research, which had been hired by the drugmakers to test their medicines.
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