Speak Pharma

This event promises to be a knowledge-sharing platform where experienced experts will share their insights to help professionals seamlessly implement acquired knowledge into practical applications. Our speakers bring a wealth of industry experience, providing you with not only theoretical foundations but also practical strategies that can be readily applied in your day-to-day operations. We understand the importance of bridging the gap between theory and practice. That’s why our speakers will share real-world examples, case studies, and best practices, empowering you to navigate the complexities of cleaning processes, CIP COP technology, and validation with confidence. Whether you are a seasoned professional or new to the field, this event caters to all levels of expertise. Join us on 7-8 November 2024, for an enriching experience that goes beyond theory, equipping you with actionable insights that will positively impact your work. Secure your spot today by submitting a request to tap into the collective expertise of our speakers and take a significant step toward enhancing your proficiency in pharmaceutical manufacturing processes. We look forward to your active participation in this collaborative learning journey with Speak Pharma. 📅 7-8 November 📍 Munich, Germany 📑 Event Page: https://lnkd.in/da4z3R6h Request full agenda today and use discount options! Speak Pharma #SpeakCleaning #CleaningValidation #PharmaHygiene #CIPAdvantages #RiskAssessment #ManufacturingQuality #ValidationStrategies #PracticalApplications #CollaborativeLearning #QA #Digitalization #Annex1

𝗢𝗽𝘁𝗶𝗺𝗶𝘇𝗶𝗻𝗴 𝗖𝗹𝗲𝗮𝗻𝗶𝗻𝗴 𝗩𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 𝗣𝗿𝗮𝗰𝘁𝗶𝗰𝗲𝘀 𝗶𝗻 𝗮 𝗖𝗼𝗺𝗽𝗹𝗲𝘅 𝗖𝗠𝗢 𝗘𝗻𝘃𝗶𝗿𝗼𝗻𝗺𝗲𝗻𝘁 Join Faidra Angelikaki, experienced 𝗣𝗵𝗮𝗿𝗺𝗮𝗰𝗲𝘂𝘁𝗶𝗰𝗮𝗹 𝗣𝗿𝗼𝗰𝗲𝘀𝘀 & 𝗖𝗹𝗲𝗮𝗻𝗶𝗻𝗴 𝗩𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 expert with over a decade of experience in manufacturing and pharmaceutical technology, for an insightful discussion on optimizing Cleaning Validation programs in a diverse #CDMO setting. 💡 𝗞𝗲𝘆 𝗧𝗼𝗽𝗶𝗰𝘀: • 𝘊𝘳𝘪𝘵𝘪𝘤𝘢𝘭 𝘤𝘰𝘯𝘴𝘪𝘥𝘦𝘳𝘢𝘵𝘪𝘰𝘯𝘴 𝘧𝘰𝘳 𝘣𝘶𝘪𝘭𝘥𝘪𝘯𝘨 𝘢 𝘴𝘶𝘤𝘤𝘦𝘴𝘴𝘧𝘶𝘭 𝘊𝘭𝘦𝘢𝘯𝘪𝘯𝘨 𝘝𝘢𝘭𝘪𝘥𝘢𝘵𝘪𝘰𝘯 𝘱𝘳𝘰𝘨𝘳𝘢𝘮 • 𝘙𝘦𝘢𝘭-𝘸𝘰𝘳𝘭𝘥 𝘴𝘵𝘳𝘢𝘵𝘦𝘨𝘪𝘦𝘴 𝘧𝘰𝘳 𝘵𝘢𝘤𝘬𝘭𝘪𝘯𝘨 𝘮𝘶𝘭𝘵𝘪-𝘱𝘳𝘰𝘥𝘶𝘤𝘵 𝘤𝘩𝘢𝘭𝘭𝘦𝘯𝘨𝘦𝘴 • 𝘛𝘩𝘦 𝘣𝘦𝘯𝘦𝘧𝘪𝘵𝘴 𝘰𝘧 𝘳𝘪𝘴𝘬-𝘣𝘢𝘴𝘦𝘥 𝘢𝘱𝘱𝘳𝘰𝘢𝘤𝘩𝘦𝘴 𝘪𝘯 𝘊𝘭𝘦𝘢𝘯𝘪𝘯𝘨 𝘝𝘢𝘭𝘪𝘥𝘢𝘵𝘪𝘰𝘯 • 𝘕𝘢𝘷𝘪𝘨𝘢𝘵𝘪𝘯𝘨 𝘵𝘩𝘦 𝘢𝘥𝘷𝘢𝘯𝘤𝘦𝘥 𝘊𝘭𝘦𝘢𝘯𝘪𝘯𝘨 𝘝𝘢𝘭𝘪𝘥𝘢𝘵𝘪𝘰𝘯 𝘭𝘪𝘧𝘦𝘤𝘺𝘤𝘭𝘦 As the Quality Product & Process Validation Manager at 𝗙𝗔𝗠𝗔𝗥 𝗚𝗿𝗼𝘂𝗽 and lead SME for COMPASS by FAMAR, Faidra brings a wealth of hands-on experience to deliver practical insights for enhancing quality compliance and operational efficiency. Use the promo code 𝗙𝗔𝟭𝟬 and get 𝟭𝟬% 𝗢𝗙𝗙 on any package! 𝙍𝙚𝙜𝙞𝙨𝙩𝙧𝙖𝙩𝙞𝙤𝙣 𝙇𝙞𝙣𝙠: https://lnkd.in/da4z3R6h Speak Pharma #SpeakCleaning #Annex #CleaningValidation #PharmaHygiene #IndustrionHygiene #RiskAssessment #ManufacturingQuality #ValidationStrategies #PracticalApplications #CollaborativeLearning #QA #Digitalization #CleanByDesign #CIP #COP

🔥🔥🔥 𝗟𝗮𝘀𝘁 𝗖𝗮𝗹𝗹 𝘁𝗼 𝗥𝗲𝗴𝗶𝘀𝘁𝗲𝗿! 🔥🔥🔥

🔥🔥🔥 𝗟𝗮𝘀𝘁 𝗖𝗮𝗹𝗹 𝘁𝗼 𝗥𝗲𝗴𝗶𝘀𝘁𝗲𝗿! 🔥🔥🔥 Don't miss this opportunity to meet a worldwide panel of experts and delegates. Join us as we cover essential topics in 𝗖𝗹𝗲𝗮𝗻𝗶𝗻𝗴 𝗩𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 for the upcoming year! 𝙊𝙪𝙧 𝙁𝙤𝙘𝙪𝙨: • 𝘈𝘯𝘯𝘦𝘹 1 𝘢𝘯𝘥 𝘕𝘦𝘸 𝘊𝘭𝘦𝘢𝘯𝘪𝘯𝘨 𝘗𝘳𝘢𝘤𝘵𝘪𝘤𝘦𝘴 • 𝘊𝘰𝘮𝘱𝘳𝘦𝘩𝘦𝘯𝘴𝘪𝘷𝘦 𝘙𝘪𝘴𝘬-𝘉𝘢𝘴𝘦𝘥 𝘈𝘱𝘱𝘳𝘰𝘢𝘤𝘩 • 𝘌𝘧𝘧𝘦𝘤𝘵𝘪𝘷𝘦 𝘙𝘪𝘴𝘬 𝘈𝘯𝘢𝘭𝘺𝘴𝘪𝘴 𝘢𝘯𝘥 𝘌𝘷𝘢𝘭𝘶𝘢𝘵𝘪𝘰𝘯 • 𝘊𝘐𝘗/𝘊𝘖𝘗, 𝘢𝘯𝘥 𝘚𝘐𝘗/𝘚𝘖𝘗 • 𝘊𝘊𝘚 (𝘊𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯 𝘊𝘰𝘯𝘵𝘳𝘰𝘭 𝘚𝘵𝘳𝘢𝘵𝘦𝘨𝘪𝘦𝘴) • 𝘗𝘳𝘢𝘤𝘵𝘪𝘤𝘢𝘭 𝘊𝘭𝘦𝘢𝘯𝘪𝘯𝘨 𝘗𝘳𝘰𝘤𝘦𝘴𝘴 𝘋𝘦𝘷𝘦𝘭𝘰𝘱𝘮𝘦𝘯𝘵 • 𝘙𝘰𝘣𝘶𝘴𝘵 𝘊𝘭𝘦𝘢𝘯𝘪𝘯𝘨 𝘊𝘰𝘯𝘵𝘳𝘰𝘭 𝘚𝘵𝘳𝘢𝘵𝘦𝘨𝘪𝘦𝘴 𝘢𝘯𝘥 𝘊𝘰𝘮𝘱𝘭𝘪𝘢𝘯𝘤𝘦 • 𝘖𝘱𝘵𝘪𝘮𝘪𝘻𝘦𝘥 𝘚𝘢𝘮𝘱𝘭𝘪𝘯𝘨 𝘛𝘦𝘤𝘩𝘯𝘪𝘲𝘶𝘦𝘴 𝘢𝘯𝘥 𝘈𝘯𝘢𝘭𝘺𝘵𝘪𝘤𝘢𝘭 𝘔𝘦𝘵𝘩𝘰𝘥𝘰𝘭𝘰𝘨𝘺 𝘌𝘹𝘱𝘦𝘳𝘵𝘪𝘴𝘦 • 𝘊𝘰𝘮𝘮𝘰𝘥𝘪𝘵𝘺 𝘰𝘧 𝘕𝘦𝘸 𝘊𝘭𝘦𝘢𝘯𝘪𝘯𝘨 𝘈𝘨𝘦𝘯𝘵𝘴 • 𝘋𝘪𝘨𝘪𝘵𝘢𝘭𝘪𝘻𝘢𝘵𝘪𝘰𝘯 𝘢𝘯𝘥 𝘖𝘱𝘵𝘪𝘮𝘪𝘻𝘢𝘵𝘪𝘰𝘯 𝘰𝘧 𝘊𝘭𝘦𝘢𝘯𝘪𝘯𝘨 𝘗𝘳𝘰𝘤𝘦𝘴𝘴   𝙍𝙚𝙜𝙞𝙨𝙩𝙧𝙖𝙩𝙞𝙤𝙣 𝙡𝙞𝙣𝙠: https://lnkd.in/da4z3R6h Speak Pharma #SpeakCleaning #Annex #CleaningValidation #PharmaHygiene #IndustrionHygiene #RiskAssessment #ManufacturingQuality #ValidationStrategies #PracticalApplications #CollaborativeLearning #QA #Digitalization #CleanByDesign #CIP #COP

Seeking a Digital Sales Specialist for Quascenta's PQMS Software suite (pqms.com) in US! If you are interested or know someone who might be interested, do help me spread the word: 

Join us on 𝟯𝗿𝗱 𝗗𝗲𝗰𝗲𝗺𝗯𝗲𝗿 for the 𝗖𝗹𝗲𝗮𝗻𝗿𝗼𝗼𝗺 𝗧𝗲𝗰𝗵𝗻𝗼𝗹𝗼𝗴𝘆 𝗢𝗻𝗹𝗶𝗻𝗲 𝗘𝘃𝗲𝗻𝘁, where we'll explore key advancements in 𝗦𝗶𝗻𝗴𝗹𝗲-𝗨𝘀𝗲 𝗧𝗲𝗰𝗵𝗻𝗼𝗹𝗼𝗴𝘆 (𝗦𝗨𝗧), including its 𝗮𝗱𝘃𝗮𝗻𝘁𝗮𝗴𝗲𝘀, 𝗮𝗽𝗽𝗹𝗶𝗰𝗮𝘁𝗶𝗼𝗻𝘀, and regulatory requirements in pharmaceutical manufacturing. A key session will cover the use of 𝗩𝗶𝗿𝘁𝘂𝗮𝗹 𝗥𝗲𝗮𝗹𝗶𝘁𝘆 (𝗩𝗥) 𝗶𝗻 𝗖𝗹𝗲𝗮𝗻𝗿𝗼𝗼𝗺 𝗢𝗽𝗲𝗿𝗮𝘁𝗶𝗼𝗻𝘀, highlighting how VR reduces 𝘁𝗿𝗮𝗶𝗻𝗶𝗻𝗴 𝗱𝗼𝘄𝗻𝘁𝗶𝗺𝗲 and improves 𝗽𝗲𝗿𝘀𝗼𝗻𝗻𝗲𝗹 𝗲𝗱𝘂𝗰𝗮𝘁𝗶𝗼𝗻 seamlessly and efficiently. The event will also address 𝗖𝗹𝗲𝗮𝗻𝗶𝗻𝗴 𝗶𝗻 𝗕𝗮𝗿𝗿𝗶𝗲𝗿 𝗦𝘆𝘀𝘁𝗲𝗺𝘀, focusing on 𝗖𝗼𝗻𝘁𝗮𝗺𝗶𝗻𝗮𝘁𝗶𝗼𝗻 𝗖𝗼𝗻𝘁𝗿𝗼𝗹 𝗦𝘁𝗿𝗮𝘁𝗲𝗴𝗶𝗲𝘀 (𝗖𝗖𝗦), covering 𝗽𝗲𝗿𝘀𝗼𝗻𝗻𝗲𝗹 𝗽𝗿𝗮𝗰𝘁𝗶𝗰𝗲𝘀, 𝗰𝗹𝗲𝗮𝗻𝗶𝗻𝗴, 𝗱𝗶𝘀𝗶𝗻𝗳𝗲𝗰𝘁𝗶𝗼𝗻, 𝗮𝗻𝗱 𝗼𝗽𝗲𝗿𝗮𝘁𝗼𝗿 𝗯𝗲𝗵𝗮𝘃𝗶𝗼𝗿. Additionally, you'll gain insights into 𝗔𝗻𝗻𝗲𝘅 𝟭 𝗿𝗲𝗾𝘂𝗶𝗿𝗲𝗺𝗲𝗻𝘁𝘀 and the differences between 𝗜𝘀𝗼𝗹𝗮𝘁𝗼𝗿𝘀 and 𝗥𝗔𝗕𝗦, with a focus on essential 𝗮𝘀𝗲𝗽𝘁𝗶𝗰 𝗯𝗲𝗵𝗮𝘃𝗶𝗼𝗿𝘀. Stay ahead with the latest in cleanroom technology and compliance. 📅 December 3rd 📍 Zoom 🔗 Registration: https://lnkd.in/gtN48REQ Speak Pharma #SpeakCleanroom #Annex1 #VRtraining #Aseptic #RABS #SingleUseTechnology #BarrierSystems #CCSPharma #PharmaVR #CleanroomOps #Isolators #PharmaCompliance #PharmaInnovation #AsepticTraining #CleanroomTech #SUTPharma #ContaminationControl #VRTrainingPharma #FillFinish #GMPCompliance #PharmaManufacturing #SterileProduction

Did you know that STERIS offers contract steam sterilization? 💨 Optimal for medical devices, diagnostics, drug delivery systems, and components, common uses include: ➡️ Product compatibility studies ➡️ R&D testing ➡️ Routine sterilization ➡️ Sterilization validation Using a hands-on approach, STERIS TechTeam professionals provide our Customers with tailored recommendations covering everything from product development to sterilization validation. If you’d like to learn more about our steam sterilization services and how they can transform your supply chain process, visit https://lnkd.in/ep974Xkw. #STERISAST #MedicalDevices #Sterilization #PatientSafety #SupplyChain #Manufacturing #Steam #ResearchAndDevelopment #ProductDevelopment #ProductDesign

Seeking a Digital Sales Specialist for Quascenta's PQMS Software suite (pqms.com) in Europe! If you are interested or know someone who might be interested, do help me spread the word: https://lnkd.in/gSkHfSDg #PharmaTech #JobOpportunity #Sales

For over two decades, cleaningvalidation.com has published memos on all things related to cleaning validation. We receive queries from readers seeking clarification. My presentation will focus on addressing the most common questions raised, providing attendees with practical insights and solutions to frequently encountered challenges in cleaning validation processes.