💡 Medipim chooses Verified by GS1! Accuracy and trust matter in healthcare product data. That’s why Medipim the Belgian platform with over 230,000 product references, has chosen Verified by GS1 to ensure reliable and unequivocal product identification. From medicines to cosmetics, Verified by GS1 enables Medipim to maintain exceptional data quality by using global identifiers like the GTIN. This step ensures healthcare professionals and businesses can count on accurate, standardised product information. And reliable data = better care! GS1 Belgilux is proud to support innovation driving data integrity in the pharmaceutical sector! 📢 Read the full story: https://utm.guru/uhN6u #DataQuality #GS1 #VerifiedByGS1 #HealthCareSector #Identifiers
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🎉 𝟱 𝘆𝗲𝗮𝗿𝘀 𝗼𝗳 𝗙𝗠𝗗 = 𝟱 𝘆𝗲𝗮𝗿𝘀 𝗼𝗳 𝗖𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲-𝗥𝗶𝘀𝗸 ☝ At the beginning of the Falsified Medicines Directive in 2019, the priority for most companies was to quickly find an FMD solution that could be integrated into their operational work processes. Compliance was put on the back burner. Not so with 𝗺𝗲𝗱𝗔𝘀𝗽𝗶𝘀. Right from the start, we saw compliance in FMD as one of the pillars of our solution. ❕For the first time in the pharmaceutical supply chain, data-generated error messages - are automatically sent to manufacturers and authorities❕ This not only jeopardises compliance but also the competitiveness of your company. medAspis Lean FMD ensures a clean slate, and the Active Alert Management makes your quality department happy. 🤗 🔗Would you like to find out more? You can find the link in the comments.🔗 #FMD #Quality #healthtech #Compliance
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🌟EPiC Symposium 2024 - From Complaint to Compliant: A Practical Guide to Overcome Current GMDP Challenges 🌟 Agenda Session: Recent Updates to Guidance & Regulations The first presentation on our agenda will provide an overview of recent changes to legislation and guidance and a forward look to highlight any significant planned changes which have the potential to impact the manufacture and distribution of medicinal products. The presentation aims to improve awareness and understanding to enable delegates to keep themselves up to date with changes to GMDP requirements, helping to prepare for implementation and avoid non-compliance. GMDP requires all personnel to receive continuing training appropriate to their role and duties to ensure medicinal products are fit for their intended use. Although updates and alerts are publicly available on EU and UK regulatory and industry websites and forums, this presentation is intended to provide a helpful bitesize summary of changes, so delegates can either be reassured they are up to date or be signposted to relevant reference sources for further reading. EPiC Auditors Managing Director Richard Andrews quotes; “Keeping up to date with current and future changes to GMDP guidance is an essential part of building a resilient Pharmaceutical Quality System (PQS) to ensure compliance.” To ensure you keep up to date, be sure to book your tickets for the event here; https://lnkd.in/e9xYp9wt 🎟️🎟️ #EPiCAuditors #EPiCvirtualsymposium2024 #Fromcomplainttocompliant #GMDPcompliance #inspectionreadiness #epiccauditors #pharmasymposium2024 #virtualsymposium2024 #regulatoryguidance #pharmaceuticalindustry #pharmaceuticalmanufacturing #pharmacompliance #PharmaceuticalQualitySystem
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Is your pharmacy ready for full DSCSA compliance? 🏥💊 The Drug Supply Chain Security Act (DSCSA) is transforming the pharmaceutical industry to enhance the security and safety of our drug supply chain. As we approach the final phase of compliance, it's crucial for pharmacies to ensure they meet all requirements. Key steps for compliance: Evaluate and update your processes Implement a DSCSA-compliant electronic tracking system Verify suppliers and trading partners Maintain comprehensive records Prepare for audits and inspections Achieving full compliance not only ensures patient safety but also enhances trust and operational efficiency. Act now to secure your pharmacy’s future! Learn more about DSCSA and our compliance solutions: https://lnkd.in/eDwrhPDP #PrimeRx #Pharmacy #Healthcare #DSCSA #Compliance #PharmacyManagement
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I will be speaking at the inaugural EPLA Conference this December in Brussels! 💊 My session, co-presented with Prof. Timo Minssen, will address the European Health Data Space (#EHDS). We'll examine its implications for the pharmaceutical industry, with particular attention to #IP rights and #tradesecret protection. Registration is now open: https://lnkd.in/dDapm7rS #EPLA #EUPharmaLegislation #EHDS #PharmaceuticalLaw
We are excited to announce that registration for the first EPLA Conference, ‘𝐑𝐞𝐟𝐨𝐫𝐦 𝐨𝐟 𝐭𝐡𝐞 𝐄𝐔 𝐩𝐡𝐚𝐫𝐦𝐚𝐜𝐞𝐮𝐭𝐢𝐜𝐚𝐥 𝐥𝐞𝐠𝐢𝐬𝐥𝐚𝐭𝐢𝐨𝐧: 𝐜𝐡𝐚𝐥𝐥𝐞𝐧𝐠𝐞𝐬 𝐚𝐧𝐝 𝐨𝐩𝐩𝐨𝐫𝐭𝐮𝐧𝐢𝐭𝐢𝐞𝐬’ is now open! 🗓 11 December 2024 | Brussels, Belgium This one-day event is packed with four sessions offering expert insights into: 🔸Regulatory data protection and market exclusivity, including the latest trilogue negotiations and their potential impact on #patentlaw 🔸Medicinal product shortages and ensuring supply security 🔸The European Health Data Space (#EHDS) and its cross-border implications for the industry 🔸Recent developments in medicinal product advertising Limited spots available, so don’t miss your chance to join us! 👉https://lnkd.in/dDapm7rS Stay tuned for the full programme and we look forward to welcoming you to Brussels! #EPLA #EUPharmaLegislation #MedicinesShortages #MedicalAdvertising
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🌐 Pharmaceutical supply chains globally are increasingly under threat from #counterfeiting and #diversion - a concern not only for patient safety but also for the preservation of brand integrity. In collaboration with GS1, we are proactively addressing the rising issue of counterfeiting within the realm of pharmaceutical supply chains. This strategic partnership aims to augment both security and efficiency, whilst ensuring robust product authentication and adherence to compliance regulations. By merging our strengths, we are making headway in devising innovative solutions to facilitate product authentication, traceability, and regulatory compliance. Learn more: 🎯 https://lnkd.in/epU4a6ri #pharmaceuticalsecurity #GS1partnership #brandProtection #traceability #supplychain #supplychainmanagement Jim Waters, Joseph Lipari Adam Robinson Adam Bartlett Carl-Rainer Stetter Joan Leka Remi Turbet Delof Paulo Machado Lou Ann Hodges John Yatsko Renee Bousson Chris (CJ) Hatt David Collins Charu Verma Pandey
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#Medical_Device_Regulatory_Affairs Market Insights, Trends & Future Development Status Recorded during 2023-2032 >> https://lnkd.in/d9KnTrdQ #Medical device #regulatory affairs regulate medical #devices, #pharmaceuticals, and #agrochemicals. This is a part of #government affairs. They hold a very crucial #position in the #healthcare industry. Their work is to #check and make #sure that #safe and #effective medical items are available everywhere. ICON plc, Emergo, Freyr Solutions, Laboratory Corporation of America Holdings, IQVIA, INTERTEK GROUP PLC, SGS Société Générale de Surveillance Holding (Deutschland) GmbH ProMEDICA International (Canada), Integer Holdings Corporation, Medpace #medicaldevice #regulatoryaffairs #pharmaceuticals #agrochemicals #safe #medicaltechnologies #healthcareindustry
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In the pharmaceutical industry, getting the right product to the right patient can be a matter of life or death. That’s why track-and-trace technology is essential. It provides real-time visibility into the entire supply chain: every touchpoint, from first mile to last-mile, must be monitored to guarantee safety, quality, and compliance with regulations like the Drug Supply Chain Security Act (DSCSA), which will become even more important come November when DSCSA enforcement begins. For pharmaceutical companies and healthcare providers, this technology not only ensures accountability but also builds trust with customers, healthcare providers, and regulatory bodies. By scanning each package and maintaining a secure chain of custody, we reduce the risk of errors and potential tampering and improve overall operational efficiency. Ultimately, track-and-trace technology is about more than logistics — it’s about safeguarding patient health and strengthening the pharmaceutical industry’s integrity. How are you improving transparency in your pharmaceutical supply chain? #PharmaLogistics #TrackAndTrace #SupplyChainInnovation #PatientSafety #PharmaCompliance #TechInHealthcare #HealthcareLogistics
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The Louisiana Board of Drug & Device Distributors report on DSCSA readiness uncovered concerning statistics ahead of the November deadline. In responses from licensees across 40 states: - Only 75% have verification procedures in place - A mere 45% are prepared for handling exceptions Ensuring pharmaceutical safety and authenticity for patients goes beyond compliance—it’s crucial. If your company isn’t fully ready, it’s time to act. Delays could risk patient safety and business operations. Contact me at SECURE@CriterionConsultingLLC.com for assistance. #DSCSA #PharmaCompliance #SupplyChainSecurity #PatientSafety #Compliance #Healthcare #Traceability [Link to Report] https://lnkd.in/dgkJ-pTY
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🤔 Which do you think are the 𝗹𝗲𝗮𝗱𝗶𝗻𝗴 𝗖𝗗𝗠𝗢 𝗰𝗼𝘂𝗻𝘁𝗿𝗶𝗲𝘀 𝗳𝗼𝗿 𝗳𝗶𝗻𝗶𝘀𝗵𝗲𝗱 𝗱𝗼𝘀𝗮𝗴𝗲 𝗳𝗼𝗿𝗺𝘀? ❓ France 🇫🇷 Italy 🇮🇹 and Germany 🇩🇪 benefit from “a well-established pharmaceutical industry, regulatory compliance, skilled workforce, advanced infrastructure, innovation, proximity to markets, and government support” 𝘾𝙤𝙪𝙣𝙩𝙧𝙮 𝙡𝙞𝙨𝙩 𝙬𝙞𝙩𝙝 𝙣𝙪𝙢𝙗𝙚𝙧 𝙤𝙛 𝙛𝙖𝙘𝙞𝙡𝙞𝙩𝙞𝙚𝙨: France - 83 Italy - 74 Germany - 73 Spain - 48 UK - 29 Greece - 21 Switzerland - 21 Poland - 20 Portugal - 17 Turkey - 17 Sweden - 14 Belgium - 11 Ireland - 9 Austria - 8 Bulgaria - 8 Romania - 8 Netherlands - 7 Czech Republic - 5 Denmark - 5 Malta - 5 Source: PharmaSource 1. Download the latest hi-res infographic here: https://lnkd.in/gNxpEmbx 2. Add your company here if it's missing: https://lnkd.in/gSweD5fX #CDMO #Pharma #FDF
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Nele Deprez