🤔 Are you in food, pharma, clinical or environmental sector? No matter the sector you operate in, QuoData is here to support you! Our expertise in proficiency testing (PT) strategies is designed to address the specific challenges across various industries, ensuring compliance and improving quality measures. ✨ Why QuoData? 👉 Industry-specific insights and solutions 👉 Deep knowledge of ISO standards, including ISO 13528 and ISO 17043 👉 Proven strategies to enhance your ROI Let's collaborate to advance your proficiency testing practices and prepare your organization for future success! Contact us today! #ProficiencyTesting #QualityAssurance
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Simplify Your Data Compliance with SciDAP Data compliance is essential in pharma, where precision is non-negotiable. SciDAP’s open-source workflows and transparency offer full visibility, supporting regulatory requirements. Reduce errors and ensure data integrity with SciDAP. Explore how SciDAP makes compliance easier—book a demo today! https://lnkd.in/eM8kWGYE
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🎃Special post for Halloween week!🎃 When your decision-making relies on yesterday’s data… 💀 In fast-paced, regulated industries, timely, accurate data is everything. Waiting around can cost valuable opportunities for improvement and compliance. Knowing what is happening in your facility at a glance, and how that ties into all of your operations is crucial. At GMP Pros, we’re helping clients streamline real-time data solutions for visualization so they can act today, not tomorrow. 📊💡 #DigitalTransformation #RealTimeData #LifeSciences #Manufacturing #DataDrivenDecisions #GMPPros #DataVisualization #pharma
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New regulations are accelerating the need for large, global, multi-business companies to harmonize policies, standards and platforms, and causing companies like Thermo Fisher Scientific to turn to new quality management system (QMS) software that can meet as many needs as possible. Technology harmonization results in better functionality, faster user proficiency, greater collaboration across borders and businesses, easier updates and better support - all at significantly lower costs. This Medical Product Outsourcing (MPO) article, guest authored by Seth Goldenberg, Vice President of Veeva MedTech, shares the perspectives of different leaders including Davina Rosen Marano of the U.S. Food and Drug Administration (FDA), Elizabeth Platt of Bio-Rad Laboratories and me. At Thermo Fisher, we’re building a building a more effective and efficient Quality & Regulatory Affairs organization - made to scale at speed, comply with government requirements and better meet the needs of the many businesses we support, today and into the future. #QualityProfessionals #QualityAssurance #RegulatoryAffairs #QARA #Regulatory #Quality #QualityControl #ThermoFisher #QMSR #eSTAR #FDA #medtech #MedicalProductOutsourcing #QMS #harmonization https://lnkd.in/guMvDCda
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At our core, it's all about quality. . Our rigorous quality control ensures that every batch meets the highest industry standards. 🔬 . #QualityAssurance #PharmaQuality #MedicineProduction #PharmaChallenges #IndustrySolutions #MedicineManufacturing #PharmaceuticalSolutions #MedicineProduction #PrivateLabel #PharmaServices #B2BManufacturing #CustomSolutions #PharmaProduction #GlobalManufacturing #MedicineProduction #B2BPharma #HealthTech
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Many of our customers have shared their experiences with #CloudLIMS and how it has transformed their labs - from seamless automation to improved compliance and efficiency. Whether you’re managing diagnostic samples, testing cannabis, or analyzing water quality, our state-of-the-art LIMS makes it effortless. Read our customer reviews and see how CloudLIMS is empowering labs across industries. https://lnkd.in/dpQtZacm #happycustomers #labs #laboratories #Customerreviews
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I am honored and thrilled to be presenting at Breakfast Session 8: Building a Bridge: Leveraging Data Governance Towards the Adoption of Emerging Technologies at the upcoming 33rd Annual PDA - Parenteral Drug Association/FDA Joint Regulatory Conference. 🤖We live in an exciting time! Digital transformation, data science, and the power of emerging technologies like AI are propelling the life science industry towards endless opportunities to better serve patients around the world. In this session, titled "Paving the Way for Innovation and Compliance Through Data Governance," I’ll dive into how regulated data—our most essential asset—plays a critical role in this evolution. In a GxP environment, assuring the integrity of regulated data is not just a necessity but a regulatory requirement. Many organizations are now integrating formal data governance programs within their Quality Management Systems (QMS) to meet these demands. I’ll be discussing how, in our rapidly evolving and innovative ecosystem, data governance is mission critical. We’ll explore how establishing strong principles and measures can build a bridge toward the compliant adoption of emerging technologies. 🗓️ Session Date: Wednesday, September 11th, 2024 🕒 Time: 7:15 AM EST ☕I hope you can join me bright and early for this talk and Q&A. Let’s embrace innovation and work together to ensure the integrity and compliance that our industry demands! ⏰Not registered yet? No problem, there's still time. Link: https://lnkd.in/ekpWtv-8 #PDAFDA2024 #DataGovernance #EmergingTechnologies #PharmaInnovation #Compliance #HenriciGroup #Leadership #PharmaIndustry
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👉 It will be an honor for me to guide you through this exciting event. I can't wait to welcome our participants! 👉 Will you be joining us? Let me know in the comments! #StudyGen360 #Bioanalytics #StudyReports #ClinicalTrials
Speaker Announcement | Coffee Talk We are excited to introduce our speakers for the upcoming Coffee Talk hosted by up to data on "Enabling Standardized Multi-Run Assay-Control": Norbert Bittner, CEO of up to data Franziska Rakitin, M.Sc., Customer Engagement Manager at up to data Join them as they share valuable insights on forward-thinking strategies for mitigating risks in assay performance. Learn how to: - Implement standardized control measures for multi-run assays while adhering to GxP standards - Discover strategies to strengthen the quality and reproducibility of your assay results - Understand how standardized multi-run assay controls can lead to more efficient use of resources Click the link to register for free: https://lnkd.in/ewr-c4v5 #StudyGen360 #Bioanalytics #StudyReports #ClinicalTrials
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Thankyou Pharmacozyme, for an engaging online webinar! Gained valuable insights on quality control strategies, tools and industry trends. #Qualitycontrol #Webinar #Pharmacozyme #Professionaldevelopment
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Don't let opportunities for improvement pass you by! At RC REDOL, we are excited about the transformative potential that Scilife's electronic quality management system (eQMS) offers! This isn't just a quality system - it's a move towards a more synergistic and integrated working environment that allows you to: ✔️ Automate complex processes - Say goodbye to redundant paperwork and time-consuming manual processes! ✔️ Unite teams - Foster a culture of quality among your teams and equip them with the tools they need to succeed. ✔️ Achieve traceability and data integrity - Maintaining regulatory compliance becomes a breeze when every data point is at your fingertips, integrated into your daily workflow. In any pharmaceutical laboratory, quality isn't just part of the business - it's what drives improvement, every day! Join us in adopting a strategic approach to quality management and book a demo where you can discover how Scilife can make your company grow. #Scilife #eQMS #QualityManagement #Automation #DataIntegrity #Traceability
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🌐 Addressing Today’s Challenges in Life Sciences: How QPharma Can Help In today’s rapidly evolving landscape, life science companies are facing unprecedented challenges. From navigating complex regulatory requirements to maintaining product quality and ensuring patient safety, the stakes are high—and so are the demands. Many companies are struggling to keep pace with: • 📈 Increasing regulatory scrutiny and compliance requirements • 🧑⚕️ Evolving industry standards and quality expectations • 🔄 Managing complex supply chains and mitigating risk • 💻 Adapting to digital transformation and data integrity demands • 💡 Developing a culture of continuous improvement At QPharma, we’re here to help organizations overcome these obstacles with tailored solutions that enhance compliance, strengthen quality systems, and drive sustainable growth. Our experts provide services across remediation, quality systems consulting, training, and regulatory support to empower your team to meet today’s challenges head-on. Partner with QPharma to turn obstacles into opportunities, setting a foundation for long-term success and innovation. If you're anticipating any projects in these areas, what are you waiting for? Let's connect to see if we can help in any way. Send me a DM to set up a quick chat #LifeSciences #Compliance #QPharma #QualityAssurance #RegulatoryAffairs #ContinuousImprovement #Innovation
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