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🔬Proveris Laboratories’ study highlights the essential role of Spray Pattern analysis in pinpointing the optimal device and formulation combination during the early phases of drug development. This analysis is pivotal for the advancement of both innovator and generic drugs, aligning with global regulatory standards. 🌬️📊 🌐Recognized by the US FDA, Spray Pattern evaluation is a crucial test for determining the in vitro bioavailability and bioequivalence of medications delivered through nasal aerosols or sprays. The European Medicines Agency (EMA) also lists it as a standard test for the quality specifications of inhalation and nasal medicinal products. 🔽 Download https://lnkd.in/dKU2jCyn to learn how drug developers and delivery system designers are gaining insights into: 1.      The impact of actuators on product performance 2.      The influence of viscosity on spray performance 3.      The evaluation of device/formulation compatibility 🤝 Contact us for expert assistance https://lnkd.in/eu-MTGKq. For further insights: FDA Guidelines on Bioavailability and Bioequivalence https://lnkd.in/dHm34zhk. EMA Guidelines on Inhalation and Nasal Product Quality https://lnkd.in/eKA-Twny #PharmaceuticalQuality #EMA #FDA #ProverisLabs #NasalSpray #DrugDevelopment #Bioavailability #Bioequivalence #SprayPattern #PlumeGeometry #LaboratoryTestServices #ProverisLaboratories

🔺Decoding the Colors of Drug Approvals: A Purple and Orange Book Primer Ever wondered what goes into getting that medication on the shelf? The US Food and Drug Administration (FDA) plays a vital role, and their resources like the Purple and Orange Books are key! Orange You Curious? 🟠🟠 The Orange Book, formally known as "Approved Drug Products with Therapeutic Equivalence Evaluations," is your one-stop shop for approved drugs in the US. It tells you if a generic drug is therapeutically equivalent to its brand-name counterpart, meaning they have the same safety, effectiveness, and performance. Feeling Purple-xed? 🟣🟣 The Purple Book focuses on biological products, which are a complex and growing category. It lists licensed biological products, including biosimilars, which are highly similar to existing, FDA-approved biological products. Why should you care? These resources are crucial for healthcare professionals, pharmacists, and anyone interested in understanding the landscape of medications. They promote: ⚫Informed Decisions: Knowing if a generic drug is therapeutically equivalent allows for cost-effective options. ⚫Transparency: Both books provide valuable insights into drug development and approval. ⚫Competition: The Orange Book fosters competition in the market, potentially leading to lower drug prices. Want to learn more? The FDA provides easy access to both books online. Let's leverage these resources to promote a more informed healthcare landscape! #pharma #drugdevelopment #FDA #healthcare #generics #biologics Feel free to share your thoughts on the importance of drug approvals in the comments!

𝐁𝐫𝐢𝐠𝐡𝐭 𝐅𝐮𝐭𝐮𝐫𝐞 𝐀𝐡𝐞𝐚𝐝: 𝐄𝐱𝐩𝐥𝐨𝐫𝐢𝐧𝐠 𝐆𝐫𝐨𝐰𝐭𝐡 𝐢𝐧 𝐭𝐡𝐞 𝐏𝐡𝐚𝐫𝐦𝐚 𝐚𝐧𝐝 𝐂𝐨𝐬𝐦𝐞𝐭𝐢𝐜𝐬 [𝐏𝐃𝐅 𝐆𝐮𝐢𝐝𝐞] #𝙈𝘼𝙍𝙆𝙀𝙏_𝙎𝘾𝙊𝙋𝙀 : The "Global Pharma and Cosmetics Market Analysis to 2031" is a specialized and in-depth study of the healthcare industry with a special focus on the #global market trend analysis. The #report aims to provide an overview of the Pharma and #Cosmetics market with detailed market #segmentation by application, type, and distribution. The report provides key statistics on the market status of the leading #Pharma and Cosmetics market players and offers key trends and opportunities in the market. 𝐆𝐞𝐭 𝐅𝐫𝐞𝐞 𝐒𝐚𝐦𝐩𝐥𝐞 𝐥𝐢𝐧𝐤 👉: @ https://lnkd.in/d49iTxJe #pharma #pharmacy #pharmacist #medicine #health #pharmaceutical #healthcare #pharmacology #medical #pharmaceuticals #gpat #pharmacystudent #pharmacists #pharmd #pharmacylife #covid #pharmacyschool #pharmacytechnician #farmacia #doctor #science #niper #doctors #pharmacymemes #biotech #pharmacistlife #pharmaindustry #pharmaceutics #pharmaceuticalindustry

As part of #GlobalBiosimilarsWeek, we're highlighting a curated collection of DDReg's insightful blogs on biosimilars, showcasing our deep understanding of regulatory strategies, market trends, and the ever-evolving landscape of biosimilar approvals. Swipe through to explore: 🔍Pharmacovigilance for Biosimilars vs pharmacovigilance for generics- https://lnkd.in/dSX-8GbR 💡 Formal Meetings for Biosimilar Product Development with the US FDA- https://lnkd.in/dMAQAgfS 📊 Evaluating the need for comparative clinical efficacy studies in biosimilar development- https://lnkd.in/d7R5pRF9 💬Effective Communication for the Safe Use of Biosimilars- https://lnkd.in/gFwg6PWm 👉Understanding Post-Approval Manufacturing Changes in Biosimilars and Interchangeable Products in USA- https://lnkd.in/ghZmVMqR Whether you're in regulatory affairs, clinical trials, or pharma strategy, DDReg Pharma Pvt. Ltd. has the tools and knowledge to support your journey in the biosimilars sector. Let’s drive innovation and accessibility in healthcare together! 💉 Contact us today: 📧 info@ddregpharma.com 🌐 www.ddregpharma.com ❓ Submit your query here: https://lnkd.in/dky_SKD7 #Biosimilars #DDReg #Pharma #RegulatoryInsights #BiosimilarWeek #GlobalPharma #InnovationInHealthcare #RegulatoryAffairs #PharmaRegulatory

Spray Pattern and Plume Geometry are stated regulatory guidance tests (now also EMA draft guidance for inhalation and nasal sprays - updated April 2024). The earlier these tests are performed in OINDP product development the greater the value- use spray characterization data to drive and expedite your product development decisions: 1.      The impact of actuators on product performance 2.      The influence of viscosity on spray performance 3.      The evaluation of device/formulation compatibility

𝗖𝗮𝗹𝗹 𝗳𝗼𝗿 𝗽𝗮𝗽𝗲𝗿𝘀 – 𝗘𝘅𝗰𝗶𝗽𝗶𝗲𝗻𝘁𝘀: 𝗻𝗲𝘄 𝗼𝗽𝗽𝗼𝗿𝘁𝘂𝗻𝗶𝘁𝗶𝗲𝘀 𝗳𝗼𝗿 𝗰𝗼𝗺𝗽𝗹𝗲𝘅 𝗰𝗵𝗮𝗹𝗹𝗲𝗻𝗴𝗲𝘀 Innovative drug formulations rely not only on active ingredients, but also on excipients. These vital substances enhance drug stability, delivery, and effectiveness, ensuring medications perform as intended and improve patient outcomes. We are happy to announce that Sharareh Salar-Behzadi, Karsten Mäder and Michael Herbig are guest editors in the European Journal of Pharmaceutics and Biopharmaceutics Special Issue: 𝘌𝘹𝘤𝘪𝘱𝘪𝘦𝘯𝘵𝘴: 𝘯𝘦𝘸 𝘰𝘱𝘱𝘰𝘳𝘵𝘶𝘯𝘪𝘵𝘪𝘦𝘴 𝘧𝘰𝘳 𝘤𝘰𝘮𝘱𝘭𝘦𝘹 𝘤𝘩𝘢𝘭𝘭𝘦𝘯𝘨𝘦𝘴. If you’d like to be part of this special issue, submit your manuscript by February 28, 2025, and choose the article type ‘VSI: Excipients.’ Learn more about the journal and submission process here: https://lnkd.in/eCKtyVei #excipients