Catalent Pharma Solutions’ Post

Unleashing the full potential of ASDs requires integrated optimization of formulations and processes, leveraging integrated high throughput development platforms to reduce time to Phase I/IND and enable continuous direct compression of engineered spray dried dispersions.   Join Hovione team at the Global DDF Summit (Drug Delivery & Formulation) in Berlin and don’t miss Inês Ramos and Pedro Monteiro's presentation 'Manufacturing Amorphous Solid Dispersions for Continuous Direct Compression: Streamlining End-to-End Formulation and Process Development'. This includes how to select the best excipients, even alternative ones to broaden the formulation landscape, and deliver a commercially viable process to obtain final oral dosage forms by Continuous Direct Compression.   Meet our experts – Table No. 16 – and learn how we can maximize the potential of your ASD development and streamline your drug product processes: https://lnkd.in/g7Yjhaeb   #DDFSummit #drugformulation #smallmolecules #drugdelivery #bioavailability #spraydrying #solubility #cdmo #initforlife

Why choose SeraNovo for your protein degrader formulations? Our proprietary technology elevates protein degrader bioavailability by 2x through enhanced solubility and permeability. Experience streamlined development & rapid formulation design compared to other formulation techniques. The use of liquid capsules further simplifies manufacturing and ensures easy clinical access. Explore more: https://lnkd.in/g3F9a4c3 Send us a message or e-mail us directly to discuss your formulation challenges. #SeraNovo #SolvingtheInsoluble #Proteindegrader #molecularglue #formulationdevelopment 

🚀 Elevate your protein degrader formulations with SeraNovo! Our proprietary technology doubles bioavailability through enhanced solubility and permeability. Get in touch with us today about your formulation challenges! #SeraNovo #SolvingtheInsoluble #Proteindegrader #MolecularGlue #FormulationDevelopment

** 📬 ** Have you seen our latest Pharma inFocus newsletter? This is the perfect opportunity to get a better understanding of the broad range of solutions the Coperion Food, Health & Nutrition Division is now able to provide!  Read how DIOSNA , Gabler Engineering GmbH and Coperion K-Tron join forces to offer a complete pharma system covering all the steps from mixing, feeding, extrusion up to spheronizing, drying and coating. Learn why VMI Mixing Solutions consistent mixing technology ensures reliable scale-up from laboratory to production scale in cosmetics production and get an insight into the broad range of pharma systems for both batch and continuous processing provided by Schenck Process Food and Performance Materials (FPM). Last but not least, read about an interesting customer story and learn how Gabler Engineering GmbH helped Wiewelhove GmbH to switch from a manual to an automated production set-up for improved process and batch control. Access the newsletter here 👉 https://lnkd.in/eS-YtA5j   #ProcessTechnology #pharmaceuticals #feeding #mixing #coating #spheronizing #extrusion 

Medical progress opens up new perspectives for the health of humans and animals. However, the development and production of modern, innovative #activeingredients also requires increasingly complex manufacturing processes. BHS-Sonthofen is manufacturing a fully welded vertical vacuum #dryer made of the special material #Hastelloy for an international customer. Read more 👉 https://lnkd.in/dEAKQ9f6 #pharma #api #processtechnology

Sending Natoli Scientific your sample for this Material Characterization is an important step in developing your tablet’s formulation! SAVE MONEY on manufacturing issues that may arise in production by getting your formula tested now REDUCE DOWNTIME by testing your formula for production issues prior to manufacturing They test and predict: Picking/Sticking problems Moisture content Capping/Lamination issues Particle size distribution Compression studies assess: Compressibility Compactibility Tabletability Outsourced Pharma

Choosing the correct excipient, lyoprotectant or cryoprotectant can be tricky when working with complex materials! Biopharma Group has over 30 years of experience when it comes to developing and optimising liquid and dried products. Some of the most common challenges that we see when it comes to choosing excipients include: ➡️ Compatibility with other ingredients ➡️ Biocompatibility and safety ➡️ Maintaining sample stability ➡️ Manufacturing and dose uniformity ➡️ Supply chain and availability of materials ➡️ Global regulatory requirements If you are experiencing any of these challenges then contact us today: https://bit.ly/3H9yivP #excipientselection #formulationdevelopment #freezedrying #optimisation #lyophilisation #liquid #compatibility #samplestability #BiopharmaGroup #CDMO

In the medical and healthcare industry, there is an increasing demand for prefilled syringes as a drug delivery format. It offers various advantages such as ease of drug handling, high dosing accuracy, and maintaining drug stability. This form of drug delivery system minimizes potential contamination from bacteria, which further ensures patient safety. Dual chamber syringes combine the storage of a powder and a diluent into one primary packaging. By simply exerting pressure on the plunger, the liquid of the lower chamber is forced into the chamber that houses the drug substance, allowing the content of both chambers to be mixed and easily administered. This simplifies the administration process and ensures a longer shelf life of the drug substance, which provides great advantages compared with conventional vial drug delivery systems. Learn about the challenges of the DCS filling manufacturing market and how to overcome them. Giel van Veen, Dec Group

🎥 Exciting News Alert! 🎥 Curious about the intricate process behind compounding pharmaceutical formulations? 🧪 Our latest video dives deep into the meticulous steps involved, showcasing how we utilize cutting-edge technology to streamline the compounding process while prioritizing accuracy and safety. 🔍 In this video, you'll discover: A step-by-step walkthrough of compounding using a Medisca reference formula. Automatic calculation of ingredient percentages, reducing the need for manual computations and minimizing human error. Integration of quality processes within the formula, ensuring top-notch standards. Access to the reference formula for documentation purposes. Configuration options for devices, pricing, and labeling to maintain consistency. Risk assessment protocols to address potential concerns before compounding begins. Real-time monitoring of ingredient weights using integrated balances for added validation. Detailed documentation of processes, including pre-compounding checklists and capsule quality analysis. Utilization of an internal chemical reference system to enhance patient safety. Transparent tracking of batches and timestamps throughout the compounding journey. Direct linkage from reference formula to Certificate of Analysis (CofA) for comprehensive insights. Watch the video now to witness the seamless integration of technology and pharmaceutical expertise in compounding excellence! 💊💡 https://lnkd.in/gvwg-mAX #PharmaceuticalCompounding #InnovationInHealthcare #PatientSafety #QualityAssurance #Medisca #TechnologyIntegration #CompoundDirect

See how Agilent helped Laurus Labs overcome analytical demands of trace-level quantitation of N-nitrosamine in challenging APIs and formulation products. Read case study and find other resources. https://bit.ly/3tNpchF #nitrosamines #pharmaimpurities