Publicación de Pablo Serrano

𝐃𝐢𝐬𝐜𝐨𝐯𝐞𝐫 𝐭𝐡𝐞 𝐤𝐞𝐲 𝐭𝐨 𝐞𝐧𝐬𝐮𝐫𝐢𝐧𝐠 𝐝𝐫𝐮𝐠 𝐬𝐭𝐚𝐛𝐢𝐥𝐢𝐭𝐲 𝐚𝐧𝐝 𝐫𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐜𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐜𝐞 𝐰𝐢𝐭𝐡 𝐨𝐮𝐫 𝐧𝐞𝐰 𝐰𝐡𝐢𝐭𝐞 𝐩𝐚𝐩𝐞𝐫 𝐨𝐧 𝐟𝐨𝐫𝐜𝐞𝐝 𝐝𝐞𝐠𝐫𝐚𝐝𝐚𝐭𝐢𝐨𝐧 𝐬𝐭𝐮𝐝𝐢𝐞𝐬! This essential guide integrates industry insights, scientific literature, and regulatory guidelines to help you design effective stress testing protocols. Learn how to identify real-world degradation pathways, create robust stability-indicating methods, and enhance drug approval and formulation processes. Enhance your pharmaceutical testing and development with our white paper: https://okt.to/DwQUnF #Pharmaceutical #stresstesting #ImpurityStandards #impurities #APIs #ReferenceStandards

Discover how desiccants impact product stability and shelf life. Our latest blog post explores the longevity of desiccants and their crucial role in maintaining pharmaceutical integrity. Stay informed with Colorcon Insights! https://hubs.li/Q02DBzBH0 #Pharmaceuticals #Desiccants #ProductStability

Effective drug stability starts with moisture control. Learn how bulk desiccants play a crucial role in maintaining the integrity of pharmaceutical products, ensuring they stay dry and potent throughout their shelf life. Dive into the latest insights on moisture management from Colorcon. https://hubs.li/Q02MM3w30

Demonstrating equivalence for generic topical pharmaceuticals can be complex. This on-demand webinar breaks down the rheology requirements outlined by FDA and EMA, covering key concepts like viscoelastic moduli, yield stress, and thixotropy. https://lnkd.in/e-CSuKAE Learn how to generate the data you need with confidence. #Pharma #Pharmaceuticals #PharmaIndustry

Unlock Your 340B Potential! 🗝 Are you feeling lost in the maze of 340B compliance? Worried about revenue leaks and complex pharmaceutical processes? 😰 Take a deep dive with Bob Steller and gain practical tips and actionable strategies for confidently managing your 340B program. 👍 Check out our latest blog here: https://vistex.link/3Qh #Pharmaceutical #RegulatoryCompliance #RevenueManagement

Discover the invisible protectors in pharmaceutical packaging: oxygen scavengers. Learn how they safeguard product stability and extend shelf life in our latest blog. Dive into the science behind these crucial additives with Colorcon Insights ⬇️ https://hubs.li/Q02HHhsK0 #PharmaceuticalPackaging #OxygenScavengers #ProductStability

Explore the intricate journey from powder to tablet in the pharmaceutical industry. Discover how film coating enhances appearance, stability, and performance. Read more: https://hubs.li/Q02y9J7D0 #pharmaceuticals #filmcoating

Modulated DSC offers unique advantages for pharma testing, including 📈 separating overlapping transitions 🔍 maintaining high sensitivity at low heating rates. Learn more in this app note: https://lnkd.in/eCgDNART #Pharma #Pharmaceuticals

A Contamination Control Strategy (CCS) should be implemented across the facility in order to define all critical control points and to assess the effectiveness of all the controls (design, procedural, technical and organisational) and monitoring measures employed to manage risks to medicinal product quality and safety. Here I am presenting the CCS elements for the pharmaceutical industry, so plz read and gives the valuable feedback. Thanks Arvind Kumar srivastava

𝗖𝗹𝗲𝗮𝗻𝗿𝗼𝗼𝗺 𝗦𝘁𝗮𝗻𝗱𝗮𝗿𝗱𝘀 𝗮𝗻𝗱 𝗚𝘂𝗶𝗱𝗲𝗹𝗶𝗻𝗲𝘀 - 𝗣𝗮𝗿𝘁 𝟯 𝗙𝗗𝗔 In the third part of our series on Cleanroom Guidelines and Standards, we explore the FDA regulations. Find our more about the FDA cGMP regulations and FDA aseptic processing guidance and see why adhering to both sets of guidelines is crucial for manufacturers to meet regulatory standards and produce high-quality, safe pharmaceutical products. This publication is the third part in our 5-part series on Guidelines & Standards. Stay tuned for more insights into quality assurance and innovation in pharmaceutical manufacturing. Link to article: https://hubs.li/Q02LSp7y0 #Cleanroom #Guidelines #FDA #STAXS