Ryoma Collia

Are you looking to streamline your artwork processes in the life sciences industry? Esko comprehensive guide provides actionable strategies to automate workflows, ensure regulatory compliance, and speed up product launches. Transform your artwork operations today! 👉 Read the guide https://ow.ly/CIfk50SNUSE

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Life sciences labeling documentation involves specific guidance for different document types, a range of regulations and requirements, varied formatting requirements for submissions, and so much more. But what if you could efficiently create and update by reusing approved content from reference labels? Learn how, with Docuvera. https://bit.ly/3UZqrsz #PharmaLabeling #SCA #Docuvera

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Is your #lab ready for a #LIMS implementation? Clarkston senior manager, Paul Allen, shares key steps for setting up your physical lab and how to optimize your lab space for a LIMS implementation. View the full guest column article here: https://hubs.ly/Q02JgWbL0 Pharmaceutical Online

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Though the benefits of #LIMS are clear, compliance can be a challenge. We're unpacking key considerations for FDA compliance when approaching a LIMS validation. https://hubs.ly/Q02DdX0s0

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Quality translations can help life science companies go global. This blog covers it all – from drug research to medical devices. Learn why teaming up with language experts is smart for biotech firms, clinical studies, and more! https://hubs.ly/Q02KTvFk0 #LifeScience #MedTech #MedicalDevices #Translation #GlobalGrowth

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WEBINAR: Only 5 days to go! Learn how to streamline your lab's compliance strategy and stay ahead of regulatory changes. Our joined CREO - Sapio Sciences expert team will share their key learnings with the audience during an exciting webinar, "Leveraging LIMS for GMP Excellence" We unravel the complexities of Good Manufacturing Practice (GMP) compliance in modern laboratories. Led by seasoned Quality Assurance experts Robin Stolzberg and Sean Blake from Sapio Sciences and Melissa Noel and Vincent Cafiso from CREO, this session will provide actionable insights and practical strategies for ensuring adherence to rigorous GMP standards. This webinar will equip the audience with the knowledge to navigate GMP compliance successfully and ensure the highest standards of quality in GMP operations. https://bit.ly/4eyij9J #LIMS #GMP #Informatics #Webinar #compliance #manufacturing #pharmaceuticals #Quality

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Here are the top 6 features to look for in a #LIMS for materials testing labs: ✔ Comprehensive Sample Management ✔ Robust Data Organization and Management ✔ Workflow Automation ✔ Quality Control and Regulatory Compliance ✔ Reporting and Operations Management ✔ Superior Document Management Learn more: https://lnkd.in/dAyC63MM Which of these features are missing in your LIMS? Write in the comments box. #MaterialsTestingLIMS #LabEfficiency #AdvancedLIMSSoftware #Materialtesting

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It was an pleasure to chat to Jason about how the #pharma industry is working to mitigate nitrosamine impurities and the evolving regulatory landscape. Check out the he podcast 👇

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[ STARLIMS guest blog post by Gregory Emmert ] Is your lab ready for a new #LIMS? Data is the backbone of lab operations, and the right LIMS is key. Discover how a channel partner can guide your team from research to full implementation. https://hubs.la/Q02Rf3jk0 #LabInformatics #DataManagement

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Are you looking to reduce your team’s administrative burdens in the regulatory content submission process? Check out the latest Life Sciences blog to learn how GenAI and machine translation workflows can mitigate risk, ensure compliance, shorten timelines and cut costs: https://bit.ly/4c3K2gu #GenAI #MachineTranslation #Regulatory #Clinical

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Online changes pose some pressing questions for pharma and will demand a new approach to website strategy   In his latest article for PMGroup Worldwide Ltd’s PME magazine DT’s Research Director Dominic Tyer looks at some of these looming headwinds.   Online changes pose some pressing questions for pharma and will demand a new approach to website strategy.   In his latest article for PMGroup Worldwide Ltd’s PME magazine DT’s Research Director Dominic Tyer looks at some of these looming headwinds.   https://lnkd.in/dDbYX3ah   #pharma #lifesciences #digitalstrategy #webstrategy #omnichannel

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Read the latest #blog from @Astrix - featuring CloudLIMS https://lnkd.in/ep7Z28rQ #lims #Laboratory #informatics #datamigration #astrix #cloudlims

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Navigating the regulatory landscape for the mandatory Annual Product Quality Review (APQR) can be challenging for pharma companies. BIOVIA's Structured Document Authoring – APQR solution streamlines the complex process of document authoring by offering key advantages: ✅ optimizes regulatory compliance ✅ reduces costs associated with APQR generation ✅ expedites time-to-market for pharmaceutical products The unified platform connects stakeholders, enabling collaboration and proactive issue management. Learn how to enhance APQR compliance, download the datasheet: http://go.3ds.com/sH3.

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🔍 Explore the latest insights on Australian UDI regulations and their impact on overseas manufacturers in our recent blog authored by Yi-Hsuan (Jenny) Lin, Senior Manager, Medical Device/IVD, at PharmaLex Australia. Learn about the compliance timeframe and labeling requirements, crucial for minimizing the potential impact on medical devices and in-vitro diagnostics (IVDs). Read the article now: https://lnkd.in/dvxxu-Jv #MedicalDevices #UDIRegulations #PharmaLex

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