Andrea Chierici - MBA

Day 2 of MEDICA - Leading International Trade Fair!🇩🇪🔝 As the sun rises over Düsseldorf for the second day of MEDICA, the energy within the halls is palpable. Watching professionals engage with our technology, from intuitive interfaces to groundbreaking functionalities, reaffirms the reason we do what we do. #Medica2024 #rehabilitation #robotic #medicine

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At #Copar, we understand the critical intersection between #plastic #production and #healthcare innovation. Let’s discover how our #industry supports the ongoing evolution of healthcare solutions. Read article in our website: Doriane-copar.com https://lnkd.in/dhWv7bzR

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☀️Unlock Your Path to Italian Market Success with Our Expertise! With over 20 years of experience, we've been at the forefront of guiding MedTech innovators and regulatory professionals toward successful registrations and global market access. Our proven track record includes helping industry leaders like VAREX Imaging, PAMPAMED, Global Instrumentation and HUAWEI streamline their product registrations in Italy. Ready to Accelerate Your Italian Market Entry? Let us help you navigate the complex regulatory landscape and expedite your path to success. Where to next? Discover how we can support your journey: https://hubs.ly/Q02Kk4VW0 #ArazyGroup #Regtech #RegtechAI #Medtech #RegulatoryAffairs #ProductRegistration #ItalyMarketAccess #GlobalMarketAccess #MedTechInnovation #ComplianceExcellence #CEMarking

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On the International Day of Radiology, we honour radiology professionals 👩‍⚕️ 👨‍⚕️ Our project proudly supports these advancements by implementing clinical audit practices across radiology and nuclear medicine in Europe, aiming to elevate quality and patient safety through evidence-based insights. On this special day, we recognize the commitment of radiology teams worldwide 🌍 #InternationalDayofRadiology #IDOR2024 #ClinicalAudit #PatientSafety #NuclearMedicine #MedicalImaging #EU4Health #HealthUnion #EUCancerPlan

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Back by Popular demand.... Want to learn more about Single-Use Endoscopes? Check out our on-demand webinar where as our Industry Experts, Grégory Grams, David “GIB” Gilbert - CISS (EO), and Jordan Elder discuss the laboratory testing and terminal sterilization considerations to help ensure regulatory compliance within the US and EU. Key topics include⤵️ ➡️Product and Packaging design ➡️Material compatibility with sterilization modalities ➡️Microbiological testing and process validation considerations to ensure a desired sterility assurance level is met ➡️Regulatory Compliance including compliance with ISO 13485 and adherence to the requirements of US and EU regulatory agencies Listen now 🎧https://lnkd.in/ePhdead8

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Introducing MedLea Srl’s Breathing Lung Platform, an #AIDriven and highly professional solution designed to transform the detection and management of #LungDiseases. The platform provides #real-time, automatic insights that enhance early diagnosis and improve #SurgicalOutcomes for patients with pulmonary conditions. MedLea Srl represents a significant advancement in #LungHealthManagement, leveraging patented #AITechnology to deliver precise, predictive analytics that support #healthcare providers in offering faster and more effective care. This leading-edge remedy aids in early detection and facilitates personalized treatment strategies for patients, ensuring the best possible outcomes. This #PatientCentric platform increases efficiency and accuracy in lung disease management, empowering healthcare providers to early detect conditions and improve care for patients, while reducing overall healthcare costs. Visit https://medlea-tech.com or get in contact with Simone Melchionna for more information. #HealthcareInnovation #PulmonaryCare #AIForHealth #LungHealth #EarlyDiagnosis

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🚀𝗟𝗮𝘂𝗻𝗰𝗵𝗶𝗻𝗴 "𝗠𝗶𝗻𝗱 𝗮𝗻𝗱 𝗛𝗲𝗮𝗿𝘁 𝗖𝗼𝗻𝘃𝗲𝗿𝘀𝗮𝘁𝗶𝗼𝗻𝘀" 𝘀𝗲𝗿𝗶𝗲𝘀, 𝘄𝗵𝗲𝗿𝗲 𝗹𝗼𝗴𝗶𝗰 𝗺𝗲𝗲𝘁𝘀 𝗰𝗼𝗺𝗽𝗮𝘀𝘀𝗶𝗼𝗻 𝗶𝗻 𝘁𝗵𝗲 𝘄𝗼𝗿𝗹𝗱 𝗼𝗳 𝗺𝗲𝗱𝗶𝗰𝗮𝗹 𝘀𝘁𝗲𝗿𝗶𝗹𝗶𝘇𝗮𝘁𝗶𝗼𝗻. 🎬𝗘𝗽𝗶𝘀𝗼𝗱𝗲 𝟭: 𝗗𝗲𝗰𝗼𝗻𝘁𝗮𝗺𝗶𝗻𝗮𝘁𝗶𝗼𝗻 𝘃𝘀. 𝗖𝗹𝗲𝗮𝗻𝗶𝗻𝗴 In today's episode, Mind and Heart will explore the critical differences between #decontamination and #cleaning, ensuring that reusable surgical instruments are safer for #PatientCare. Our new animated video answers key questions like: 👉 How do we differentiate cleaning from decontamination? 👉 What precautions must healthcare personnel take in the decontamination area? 👉 Which guiding documents should a CSSD personnel refer to? 👉 What should be looked out for, when deciding a cleaning agent? Dive into these critical insights and more! 🎥💡Whether you're a healthcare pro or just curious, this video breaks down the essentials for maintaining a safe, sterile space. Advanced Sterilization Products #WeAreASP Advanced Sterilization Products APAC #ASPAPAC #MindAndHeart #HealthcareSafety #CSSD #Decontamination #Sterilization #InfectionPrevention #HealthcareStandards #Healthcare #MedTech

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MEDTECH EUROPE position paper on EUDAMED: Smooth transition to the mandatory use of EUDAMED Perspectives from manufacturers! This paper provides the industry perspectives for a smooth transition to the mandatory use of various EUDAMED modules by efficient use of resources, building on the points of the Joint open letter: In anticipation of EUDAMED availability for mandatory use. The European central database for medical devices ‘EUDAMED’ is a critical infrastructure for the In Vitro Diagnostics (IVD) and Medical Devices (MD) Regulations. Its implementation represents an investment into a more efficient regulatory system providing oversight of devices, enhanced collaboration between Competent Authorities and users and more transparency for the public.

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Pressure ulcers, also known as bedsores, are a significant concern in long-term care settings, particularly affecting patients with limited mobility. VENDAJE's innovative DHAM allograft introduces a pivotal advancement in the support for treatment and management of these challenging wounds. What makes VENDAJE® particularly suited for pressure ulcer treatment is its ability to provide a protective barrier over the wound environment. The natural properties of the amniotic tissue, preserved through the BioRetain process, facilitate a protective environment, actively reducing inflammation and promoting rapid and effective healing. Implementing VENDAJE into the care regimen for patients at risk of or suffering from pressure ulcers can improve patient outcomes, therefore reducing treatment durations, and enhancing patient comfort and quality of life. Healthcare providers across the spectrum—from hospitals to long-term care facilities—have recognized VENDAJE as a vital tool in their efforts to treat pressure ulcers. Each of these posts emphasizes VENDAJE’s role in supporting the treatment of specific types of wounds, highlighting its benefits and encouraging healthcare professionals to consider its use in their practice. If you need further customization or additional content, feel free to let me know! #BSEM #pressureulcer #woundcare #biostem #VANDAJE #BIORETAIN

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Are you ready for #PCORI24? This year’s program features 2 incredible keynote sessions you won’t want to miss! Day 1: Explore the future of clinical trials through the lens of connection and engagement. Day 2: Discover how patients are driving innovation in the dynamic field of healthcare research. Learn more about the keynotes and explore the full agenda! https://pcori.me/3BRXtU3

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On World Patient Safety Day, Temos International reaffirms our commitment to enhancing patient safety worldwide. This year's theme, "Improving Diagnosis for Patient Safety," emphasizes the importance of accurate diagnosis in preventing errors and ensuring optimal treatment outcomes. At Temos, we recognize that this involves minimizing risks through safe practices, making accurate diagnoses, clear communication, and robust systems that support healthcare providers in delivering the best care. Temos accreditation programs focus on creating systems that enhance diagnostic safety and drive data-driven decisions that strengthen healthcare facilities clinically and operationally. Collaborating with Temos empowers healthcare leaders to address issues like malpractice and medical errors by improving communication and documentation, fostering a more cohesive medical staff for better clinical outcomes. With the guidance from Temos, healthcare leaders can enhance analytic processes and utilize data insights to drive positive change and refine patient care approaches, which ultimately reduces diagnostic errors and elevates patient safety. So on this World Patient Safety Day, let's collectively advocate for the critical role accreditation plays in achieving safer healthcare. Join us in prioritizing patient safety by partnering with Temos to elevate your healthcare facility's standards and make a meaningful impact on patient care. 🔗 www.temos-worldwide.com 📧 [email protected] #WorldPatientSafetyDay #ImprovingDiagnosis #PatientSafety #Temos #accreditation #healthcare #german #clinics #medical #expert #healthcareindustry #patientcare #patientexperience #riskmanagement #patientsafety #FAQ #healthandsafety #vision #mission #patientcentricity #reliability #ceo #benefits #careerdevelopment #network #german #worldpatientsafetyday #worldhealthorganization #patientadvocacy #WHO #UnitedNations

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The medical device outsourcing market has grown because of the increasing complexity of developing and making medical devices. It covers various services such as design, engineering, regulatory consulting, prototyping, testing, and manufacturing. As the healthcare industry advances and the demand for advanced medical devices rises, companies are using outsourcing to make their operations more efficient and get specialized help. #Medical #Device #Outsourcing Market Size, Share & Trends Analysis Report By Product (Finished goods, Electronics, Raw Materials) By Device Type (Class I Devices, Class II Devices, Class III Devices) By Services (Prototype Development, Finished Device Manufacturing, Assembly & Packaging, Testing & Regulatory Support Services) By Application (Orthopedics and Spine, Cardiovascular, Radiology, General Medical Devices, Others), Global Economy Insights, Regional Outlook, Growth Potential, Price Trends, Competitive Market Share & Forecast, 2023 - 2031 IMIR Market Research Pvt. Ltd. 📚 𝗚𝗲𝘁 𝘁𝗵𝗶𝘀 𝗿𝗲𝗽𝗼𝗿𝘁 𝗮𝘁 𝗱𝗶𝘀𝗰𝗼𝘂𝗻𝘁𝗲𝗱 𝗽𝗿𝗶𝗰𝗲👇  https://lnkd.in/g3EfCbB2 📚𝐓𝐨𝐩 𝐌𝐨𝐫𝐞 𝐊𝐞𝐲 𝐏𝐥𝐚𝐲𝐞𝐫𝐬 𝐀𝐫𝐞:👇 GXP Engaged Services GmbH H2O Clinical Heraeus House of Procurement (HOP) ICON plc inmedis GmbH Integer Holdings Corporation Intermed Oy | Service | JOINN LABORATORIES (CHINA) CO., LTD. Judex A/S Kapstone Medical KCR Placement Lifecycle Management Group LifeScience Logistics Lignum Vitae Health (LVH) LSC, Life Science Consultants Masuu Global Solutions Meytar R&D Minnesota MedTec, Inc. Moll Industries MZD GmbH Nortech Systems, Inc. NovelCath A Cirtec Company   oneservice Onex Orakris Med Solutions Orchid Orthopedic Solutions Orthofix PDC CRO PharmaLex Medical Device Services Plastic Engineering & Development, Inc.. Plexus Corp. Primo Medical Group ProductLife Group Proven Process Medical Devices Prudentia Group, LLC QTS Medical Device Outsourcing QUALITY PRODUCTION by Spronken Quanticate #outsourcing #business #virtualassistant #bpo #marketing #technology #outsource #outsourcingservices #virtualassistantservices #smallbusiness #callcenter #businessowner #workfromhome #entrepreneur #digitalmarketing #accounting #customerservice #software #o #va #payroll #telemarketing #businesssupport #virtualassistantforhire #sales #work #hr #virtualassistance #freelancer #personalassistant

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Euronda was one of the first Italian companies to obtain MDR certification for all its Medical Devices (class I, IIa and IIb). Euronda Class I medical devices have conformed to the new Regulations since May 2021. For higher-class medical devices, Euronda obtained certification in September 2021 of all Pro System autoclaves (EXL, E10, E9 and E8). In order to understand the importance of this milestone, the implications of the new Regulations for the entire medical supply chain, from manufacturer to patient, are discussed in the article. https://lnkd.in/d4kb3-ez

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Watch chapter 6 of our Guide to Conformity Series – MDSAP. Stay tuned for the upcoming chapters. To know more, visit our dedicated webpage: https://bit.ly/40zwwPt #BSI #MedicalDevices #GuidetoConformity #MDSAP

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📚 Discover our Radiology books and decision support solutions at #RSNA24! Stop by the Elsevier booth to learn more about updating your medical library with our Radiology books, as well as demoing our decision support solutions. #RSNA24 #RadiologyBooks #DecisionSupportSolutions

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The Path to Compliance: Italian Sunshine Reporting Done Right! Italian businesses in healthcare, pharmaceuticals, and medical devices are navigating uncharted waters with the Italian Sunshine Act (Law No. 62/2022). The new regulations demand a shift in mindset, moving beyond EFPIA and MedTech frameworks to meet Italy’s unique transparency requirements. But compliance is more than just ticking boxes—it’s about building trust. The Sanità Trasparente platform will make financial relationships with healthcare professionals and organizations visible to the public, underscoring the importance of accurate and timely reporting. At Vector Health, we understand the challenges Italian companies face in adapting to this new regulatory landscape. From data collection systems to error-free reporting strategies, our solutions are designed to support you every step of the way. What does the Italian Sunshine Act mean for your business? - A chance to showcase your commitment to transparency and ethics. - An opportunity to align with best practices while avoiding costly penalties. - A need to adapt systems and processes for seamless compliance. Let’s navigate this together. Whether you’re just starting or refining your compliance program, Vector Health is here to help you stay ahead. #ItalianSunshineAct #SanitàTrasparente #HealthcareCompliance #PharmaTransparency #VectorHealth #TransparencyMatter

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Avoid these pitfalls to prevent costly delays and legal problems: How to master the summative evaluation for medical devices.     We are pleased to present our latest article, which deals with a critical topic for the approval of medical devices: summative evaluations/Human Factors Validations. By reading this article, you will learn how to avoid costly delays and secure approval for your medical device.   🔍 Here are two of the biggest mistakes in summative evaluations/Human Factors Validations and how to avoid them:   ⚠️Lack of diversity in the participant group:   Problem: Biased evaluations and exclusion of important usage scenarios. Solution: Ensure a diverse group of participants to cover all potential users.   ⚠️ Unrealistic test conditions:   Problem: Results do not reflect actual usage. Solution: Simulate real conditions as accurately as possible.   Our full article contains five more of these pitfalls and their solution. You also get to know the solutions to the above problems in more detail!   👉 Read the full article and find out how to successfully master summative evaluation: https://lnkd.in/eKcepKx6   #MedicalDevices #SummativeEvaluation #ProductApproval #BestPractices #HealthcareInnovation #MedTech

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