Read our short guide ‘Compliant Library Preparation for DNA Sequencing’ Now available online for download (no webform, no details collected) https://maly.co.uk/okuda/ #DNAsequencing #processmanagement #compliancemanagement #SOP #audit #logs #pharmaceuticals #pharma #pharmaindustry #biopharma #futurereadiness #drugdevelopment #pharmapipeline #pipeline #regulatorycompliance #regulation #research #Okuda #nocode #TailoredComplianceSoftware
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Few processes are more complex than DNA sequencing. It makes an ideal case study of a repeatable process. Read this short guide ‘Compliant Library Preparation for DNA Sequencing’ Available for download (no webform, no details collected) https://maly.co.uk/okuda/ #DNAsequencing #processmanagement #compliancemanagement #SOP #audit #logs #pharmaceuticals #pharma #pharmaindustry #biopharma #futurereadiness #drugdevelopment #pharmapipeline #pipeline #regulatorycompliance #regulation #research #Okuda #nocode #TailoredComplianceSoftware #casestudy
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Missed our webinar on 'AI in the #Pharmaceutical Industry: Strategies for Regulatory Success'? No worries—you can watch the full session here! https://lnkd.in/ePvfSjnx In this session, we covered: ✅ Key strategies for regulatory success in AI implementation ✅ How to ensure compliance while innovating with AI ✅ Best practices for responsible AI in #pharma Whether you're working on AI in the pharmaceutical sector or just curious about the regulatory landscape, this is a must-watch for you! Catch up on all the insights and stay ahead in the evolving world of #AI in pharma. 🚀 #AIImplementation #ArtificialIntelligence #ResponsibleAI #AIinPharma
AI in the Pharmaceutical Industry Strategies for Regulatory Success
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The #US FDA recently unveiled a comprehensive draft guidance on Potency Assurance for #Cellular and #Genetic Therapy Products, emphasizing the critical need for standardized potency across batches. This 25-page document aims to equip #drugdeveloper with robust strategies, rooted in science and risk assessment, to guarantee consistent potency in every released batch. Ensuring uniform potency is key to achieving the intended therapeutic effect. Stay informed and delve into the details of this crucial guidance! View/Download document: https://lnkd.in/ez7kqcnS #FDA #PharmaGuidance #CellTherapy #GeneticTherapy #PotencyAssurance #PharmaIndustry #pharma #pharmaceutical #pharmaindustry #europe #pharmaceuticalindustry #healthcare
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Are you a biopharmaceutical professional in APAC? Mark your calendars to join our exclusive webinar, "Unlocking Efficiency in Formulation Development with MIFD & Simcyp Biopharmaceutics." Discover how to streamline development, make informed decisions, and leverage innovative features for faster drug development. This webinar is Ideal for drug formulation experts, and anyone interested in Virtual Bioequivalence (VBE). Register now: https://ow.ly/tTqe50Se9lg #Biopharmaceuticals #FormulationDevelopment #DrugDevelopment #SimcypBiopharmaceutics #MIFD #Webinar #Innovation
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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/ek8UVX #Pharmaceutical #DrugDevelopment #StressTesting #ForcedDegradation
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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/iNmMJv #Pharmaceutical #DrugDevelopment #StressTesting #ForcedDegradation
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Incorporating a precision medicine-based approach into clinical trial design can reduce time to market approval and save costs associated with drug development. Learn how Genemarkers can support your next trial! https://lnkd.in/eGpXKqe7 #ClinicalTrials #ClinicalTrialDesign #Pharma #ClinicalTrial #DrugDevelopment #Pharmaceuticals #PrecisionMedicine #PharmacogenomicTesting #PGxTesting
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To watch the full video, Tap the link given below! https://bit.ly/4aFHLIF Explore the pharmaceutical industry's Top 5 challenges with Mr. Sanjay Chauhan. 🤔 Uncover insights into the pressing issues, including manpower and skill shortages. 🌟 Join the conversation as he narrates the industry's hurdles and proposes solutions. Stay informed and engaged with the latest updates on the pharmaceutical landscape. #pharmaInsights #careerguidance #industryperspective #pharmajeeto #kareersity #guidance #careeradvice #pharmaindustry
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Check out our latest article in ONdrugDelivery, discussing the growing need for more clinically representative test set-ups in orally inhaled and nasal drug product (OINDP) development. Specifically, we highlight the use of more realistic inhalation flow profiles and the use of idealised mouth-throat and nasal models to accelerate product development and strengthen the utility of in vitro methods for product development and regulatory submissions. 📖 Read it now: bit.ly/3UaoKqh #Innovation #ODDmagazine #Article #Compliance #Pharma #InhalerTesting #DrivingResults #Pharmaceuticals #Formulations
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Join us for a webinar on the latest recommendations of the ICH guideline for analytical method validation! The meeting is an extraordinary opportunity to explore the principles, methods and practical examples for evaluating validation characteristics, such as precision and accuracy, according to the latest ICH Q2(R2) guidelines. During the webinar, we will discuss statistical principles for assessing precision and accuracy conducted as two separate studies and as one combined study. Examples of the application of statistical methods will be presented in a practical way to make it easier to understand how to apply the new recommendations in practice. Don’t miss the opportunity to stay up to date on the latest trends and guidelines in analytical method validation. Sign up now for our webinar and expand your knowledge together with experts! Your research deserves the best approach, and we can help you with that! 📅 Register here: https://lnkd.in/dZ3CVvjU #StatSoft #Webinar #Pharma #Biopharma #PharmaSolutions #DataScience #DrugDevelopment #DrugDiscovery #DrugManufacturing #Pharmaceutical #PharmaceuticalIndustry #ValidationMethods #ICHQ2
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