Is your pharmaceutical company struggling with slow financial close processes? We can help! Consolidate financial data from all your subsidiaries and controlled sub-companies – no matter the level – for a faster, more efficient close. Want to know more? Learn how our platform can revolutionize your financial close by scheduling a complimentary demo. Book now: https://lnkd.in/gBmSrbAg #Pharma #PharmaceuticalIndustry #Biopharma #LifeSciences #Consolidation #reporting #financialreporting #financialgoals #cpm #automation #epm #performancemanagement #10yearsofSAM #SAMCorporate
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We recently completed a benchmarking project for a savvy pharmaceutical client, helping them validate their budget assumptions for the upcoming year. Benchmarking is a fantastic way to understand how your company compares to others at the same stage in their life cycle. For Finance teams swamped with daily tasks, we can quickly gather and deliver insightful data points. Ready to see where you stand? 🌟 #Benchmarking #PharmaSuccess #PhaseForwardConsulting #FinanceInsights
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Enhance your productivity and improve the prioritization of your projects with our Pharmaceutical framework and workshops. About our Workshops: https://buff.ly/3JjB0Qs About the Framework: https://buff.ly/44rqwH9 About the Excel Dataset: https://buff.ly/3xDstpc About the Diagrams: https://buff.ly/3L3FBXJ
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Pharmaceutical Industry Leaders, Are you grappling with challenges like - regulatory compliance, - equipment downtime, or - escalating operational costs? Discover how IBM Maximo is transforming the pharmaceutical landscape by driving efficiency, compliance, and innovation. Here’s a quick look at why IBM Maximo is the ultimate Enterprise Asset Management solution for pharma companies. Swipe through to learn more 👉 #PharmaInnovation #AssetManagement #IBMMaximo #IBMMAS #MaximoApplicationSuite #PharmaLeaders
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🚀 Transform Your Pharmaceutical Operations with Cutting-Edge Software Solutions! 💊 In today’s fast-paced pharmaceutical industry, efficiency, compliance, and data management are more critical than ever. That’s why we at Geega Tech have developed a powerful, all-in-one Pharmaceutical Management Software designed to streamline your operations and help you stay ahead of the competition. 🔍 Key Features: Centralized Management: Seamlessly manage inventory, supply chain, and compliance from a single platform. Real-Time Reporting: Access crucial data instantly, enabling faster and more informed decision-making. Regulatory Compliance: Stay compliant with ever-changing regulations with automated tracking and reporting tools . Customizable Workflows: Tailor the software to fit your specific processes, ensuring maximum efficiency. 💡 Why Choose Us? With over 15 years of experience in the IT industry, Geega Tech is dedicated to delivering solutions that not only meet but exceed the unique needs of pharmaceutical companies. Our software is built to scale with your business, offering the flexibility and reliability you need in a dynamic market. 🔗 Let’s Connect! Interested in learning more? Let's discuss how our software can revolutionize your pharmaceutical operations. Schedule a quick call with me here: Calendly Link Visit our website for more details: Geega Tech Website #PharmaceuticalIndustry #SoftwareSolutions #PharmaTech #RegulatoryCompliance #Innovation #HealthcareTechnology #GeegaTech
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Today, our development team successfully delivered a Proof of Concept (POC) for managing workflows for one of the top 5 pharmaceutical companies in Pakistan! 💡 In an era where going paperless is essential, efficient workflow management plays a pivotal role. With our team's extensive experience in leading workflow software, we've now developed a customized workflow solution that is not only cost-effective but also scalable to meet diverse business needs. We're still in the beta phase, but the results are promising! 🎯 Interested in a demo? Drop a comment or message us – we’d love to show you how this can transform your business operations. #DigitalTransformation #WorkflowManagement #Pharmaceuticals #Innovation #ScalableSolutions #BetaMode #PixcileTechnologies
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The global pharmaceutical analytical testing outsourcing market size was valued at USD 8.3 billion in 2023 and is projected to grow at a CAGR of 8.4% from 2024 to 2030. https://lnkd.in/dttHMU2C Growth in the market can be attributed due to increasing focus toward safety, & quality; regulation, pricing benefits of outsourcing, and rising number of end use. Besides, increasing R&D investment is one of the critical sustainability strategies adopted by market players. As, not all companies have an infrastructure for analytical testing. Therefore, outsourcing these operations is a suitable option, which helps to save time and cost. Recent Developments · In December 2023, Agno Pharma acquired Lubrizol Particle Sciences Inc. The acquisition encompasses the drug product formulation technology integral to Particle Sciences Inc. including the PA, Bethlehem development & manufacturing site. · In November 2023, Eurofins acquired Quasfar supporting the pharmaceutical industry in Latin America, enhancing its capabilities in R&D, providing support in the early stages of pharmaceutical product development. #PharmaceuticalAnalyticalTesting #OutsourcingMarket #MarketResearch #Bioanalytical #PharmaceuticalCompanies #Biopharmaceuticals #ContractResearchOrganizations #IndustryTrends
Pharmaceutical Analytical Testing Outsourcing Market Report, 2030
grandviewresearch.com
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Enhance productivity and improve prioritization with our Pharmaceutical framework and workshops. About our Workshops: https://buff.ly/3JjB0Qs About the Framework: https://buff.ly/44rqwH9 About the Excel Dataset: https://buff.ly/3xDstpc About the Diagrams: https://buff.ly/3L3FBXJ
Pharmaceutical Framework | Business Architecture Info
businessarchitecture.info
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If you have such a model kit, how can you assemble it more perfectly? Preparing the hardware perfectly, regardless of modality or platform, is a remarkable feat. However, ensuring the quality of pharmaceuticals produced within a completed facility can be even more complex. Through #QMS and #PQMS, Quascenta integrates solutions that guarantee the full lifecycle quality of your pharmaceutical manufacturing facility. We are building a sustainable software environment that is not only compliant with global standards but also more economically viable, alongside quality. 🌈 Experience Quascenta's solution through a simple demo: [email protected] 🌈 Ensure that your valuable Quality Units can work in a better environment. 💻 Quascenta | Quascenta.com | eResiduePro.com | eProcessPro.com
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Witness the instant transformation from paper-based inefficiency to a streamlined digital workflow with noxVIEW LogSpot. This innovative solution empowers manufacturers and pharmaceutical companies to: - Eliminate paper waste and manual data entry burdens. - Gain real-time visibility into critical process parameters. - Enhance regulatory compliance through secure data management. Embrace the future of data logging. Explore noxVIEW LogSpot today! #DigitalTransformation #DataManagement #Industry40 #Manufacturing #Pharmaceuticals #noxVIEWLogSpot #CloudData #ProcessOptimization #noxVIEW #NutronSystems
Transform your data in Digital with noxVIEW LogSpot!
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I had the pleasure of interviewing Dan Bell, Senior Vice President, Innovation and Strategic Operations at Marken. Learn about the complexities of time-sensitive and temperature-sensitive logistics in the pharmaceutical industry! In Part 1 of this Orchestrating Outcomes interview, Dan Bell of Marken explains how risk analysis and patient-first workflows are key to delivering safe and highly effective products. Watch the complete video! https://bit.ly/4d2Lno5 #SupplyChain #LifeSciences #OrchestratingOutcomes Stay tuned for Part II
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