Altasciences’ Post

- Why do you need a quality target product profile? - What type of formulation studies are required for which stage of development? - What is the appropriate level of characterization ensuring safety, quality, and potency in relation to the phase of the Human Clinical Trials? Coriolis Pharma's upcoming webinar - The Road to Success: Mapping drug product development from preclinical to commercialization. February 21st, 4pm (CET) / 10am (ET) Bruce Kerwin, PhD - Scientific advisor and Dr. Eva Keilhauer - Scientist will be highlighting how DP and Clinical Development are linked, going into detail about phase-appropriate actions taken as part of a roadmap. Register here: https://lnkd.in/eBk-wmUg #CoriolisPharma #DrugProductDevelopment #PreClinical #Commercialization #PharmaDmand

The landscape of OSD drug development is evolving rapidly as companies strive to bring more innovative drugs to market. However, manufacturers face various obstacles, from cost and time pressures to overcoming the scientific development challenges and preparing for robust clinical and commercial manufacturing. In our latest insight, we dive into the opportunities set to streamline efficiency in the OSD space in 2024: https://lnkd.in/daC2wAs3 #OSD #PharmaTrends #DrugDevelopment 

Another thought piece for our latest mid-week update! This article delves deeper into Singota Solutions proficiency and experience with small batches and early-phase partners. Discover how we guide clients through the drug development pipeline to achieve successful clinical trials, while minimizing production losses along the way. #SmallBatch #EarlyPhase #CDMO #ClinicalTrials #DrugDevelopment #FormulationDevelopment #AsepticManufacturingSolutions

🔬🚀 At Zenvision Pharma LLP, innovation is our driving force! 🌟 We're not just a Contract Research Organization (CRO), we're pioneers in identifying novel products with strong intellectual property (IP) through cutting-edge research and the power of Pharma databases. 💡 Our commitment to innovation shines through our patent applications filed in India, USA, and more. 🔬 From groundbreaking Change in Route of Administration to revolutionary New Molecular Entities (NME), we're at the forefront of Product Lifecycle Management. Our versatile capabilities span Process Development, CMC, and Pharmacovigilance, tailored to meet our clients' unique needs. 🧪 Embracing the power of science, we've developed Platform Technologies that breathe new life into off-patent products, extending their lifecycle. Our formulations cater to Unmet Medical Needs, addressing challenges in ways never seen before. 💊 🌐 With over 40 patent applications, our commitment to innovation extends across international boundaries. Whether it's regulated markets like the USA and Europe or emerging markets, Zenvision is there, making a difference. 🤝 Partner with us, and experience our expertise in handling even the most complex products, including Cytotoxic, Anti-neoplastic, and Hormones. Our capabilities align seamlessly with potential 505(b)(2) candidates. 🛡️ Patents aren't just documents; they represent our dedication to protecting breakthroughs in #drug #manufacturing and formulation. At Zenvision Pharma LLP, we're not just transforming the future – we're defining it. Join us on this journey of innovation and impact! 💪🌎 #pharma #pharmaceutical #innovation #healthcare #cdmo #contractmanufacturing

A Contract Development and Manufacturing Organization (CDMO) like Frontro Pharma transforms your product concepts into cutting-edge formulations, ensuring precision and efficacy in drug delivery systems. Our comprehensive services encompass product development, preclinical studies, analytical techniques, regulatory and scientific writing, and regulatory filing, ensuring a seamless journey from concept to market. To know more visit : https://frontropharma.com/ #CDMO #ProductDevelopment #DrugDelivery #PharmaInnovation #NanoFormulations #PreclinicalStudies #AnalyticalTechniques #RegulatoryWriting #RegulatoryFiling #PharmaceuticalExcellence #Biotech #PharmaScience #FrontroPharma #ScientificExpertise #PharmaSolutions #ClinicalResearch #CRO #Nutraceuticals #CosmeticScience

[New offer] 📢 SEQENS has recently extended its offer towards a comprehensive solution from Drug Substance to Early-phase formulation for APIs. This new integrated offer, named 𝗦𝗲𝗾𝗲𝗻𝘀𝗨𝗣! combines scientific expertise to solve Drug Substance challenges, such as bioavailability challenges for example, by bringing innovation in Drug Delivery Solution in the Early-stage development of APIs. 👩🔬 Learn more about this new offer and download the brochure on our website ! 👇 📰 Interested to go further ? Read also our latest white paper about "𝗣𝗿𝗲-𝗳𝗼𝗿𝗺𝘂𝗹𝗮𝘁𝗶𝗼𝗻 𝗮𝗻𝗱 𝗘𝗮𝗿𝗹𝘆-𝗙𝗼𝗿𝗺𝘂𝗹𝗮𝘁𝗶𝗼𝗻 𝗦𝘁𝘂𝗱𝗶𝗲𝘀 𝘁𝗼 𝗗𝗿𝗶𝘃𝗲 𝗦𝘁𝗿𝗮𝘁𝗲𝗴𝗶𝗲𝘀 𝘁𝗼 𝗘𝗻𝗵𝗮𝗻𝗰𝗲 𝗗𝗿𝘂𝗴 𝗗𝗶𝘀𝘀𝗼𝗹𝘂𝘁𝗶𝗼𝗻" : 👉 https://lnkd.in/exys7ybs https://lnkd.in/e9Uc9mjh #ourscienceforyourfuture #earlyformulation #drugdevelopment #cdmo #bioavailability

Join this upcoming workshop in Copenhagen. Explore cutting-edge winning strategies to enhance drug absorption and formulation techniques for clinical success. https://ow.ly/Z38R50PqrG2

🌟NEW! Watch our webinar now: Stability Study Considerations Throughout the Drug Product Life Cycle Our expert, Megan Doran, Formulation Team Leader at Intertek Melbourn, takes you on a journey of stability study considerations throughout the drug product life cycle highlighting key challenges and analytical testing considerations from discovery and preclinical all the way to monitoring continued product performance throughout the shelf life of the drug product for commercial batches. Don't miss this excellent learning tool! 👁️🗨️Watch now: https://lnkd.in/eWh4K5TU #DrugDevelopment #DrugStability #DrugsPharmaceuticals

🌟NEW! Watch our webinar now: Stability Study Considerations Throughout the Drug Product Life Cycle Our expert, Megan Doran, Formulation Team Leader at Intertek Melbourn, takes you on a journey of stability study considerations throughout the drug product life cycle highlighting key challenges and analytical testing considerations from discovery and preclinical all the way to monitoring continued product performance throughout the shelf life of the drug product for commercial batches. Don't miss this excellent learning tool! 👁️🗨️Watch now: https://lnkd.in/eWh4K5TU #DrugDevelopment #DrugStability #DrugsPharmaceuticals

Today’s #drugdevelopers are confronted with a formidable challenge: Crafting formulations for medications that meet the rigorous standards of safety, efficacy, and suitability for patient use. Their task encompasses a meticulous consideration of three key factors: 1) optimizing molecular properties, 2) prioritizing #patientcentricity, and 3) ensuring a safe and stable end product. By addressing each of these elements, drug developers aim to not only maximize the drug’s therapeutic benefits but also minimize its associated risks, ultimately improving #patientoutcomes. Our recent blog delves into the intricate art and science of #pharmaceuticalformulation, offering insights into how a strategic partnership with a #CDMO can provide invaluable support to sponsors. You can read the blog here: http://spr.ly/6043kDlvD