eCAP Project’s Post

✨ EADV Congress 2024 ✨ For all roles in pharma, achieving congress objectives requires a different approach to the ‘day job’. David Barwick and Mark Wilson recently attended the EADV congress to support one of our partners to do just that. Check out the team in action! Get in touch with us to learn more about the holistic congress offering that was causing a stir in Amsterdam! #EADVCongress #EADVCongress2024 #CongressObjectives #EventObjectives

Brisa Advisors at FIME 2024: Connecting Innovations to the Brazilian Medical Device Market We are excited to announce that Brisa Advisors will be present at FIME 2024, the largest medical device trade show in the Americas, taking place from June 19 to 21 in Miami, USA. This event is a unique opportunity to explore the latest innovations in medical technology and discuss the newest trends in the departament. FIME brings together healthcare professionals, manufacturers, distributors, and regulators from around the world, providing a conducive environment for networking and knowledge exchange. As experts in market access and regulatory compliance with ANVISA, Brisa Advisors is committed to helping companies navigate the Brazilian market safely as your Sales Partner, ensuring the competitive effectiveness of your products. If you wish to market your products in Brazil through a strong, competitive, and highly reliable structure, schedule a conversation with our CEO, Marcelo Brisolla, and explore the best strategies Brisa Advisors can offer to expand your business in the region. During FIME, our team will be available to discuss how we can support your company in entering this market, from selecting the best sales channels, obtaining regulatory approvals, to effective commercialization. Schedule a meeting ( https://lnkd.in/dmePASFP ) at the trade show and discover how we can collaborate to accelerate the entry of your medical devices into the Brazilian market. We look forward to seeing you at FIME 2024! Click to learn more about FIME on our blog. https://lnkd.in/dpnquqJV #FIME #RegulatoryAffairs #BrisaAdvisors #BPOinRA #MedicalDevices

If you’re planning to enter Europe’s medical device sector, this is a must-attend event. Experts from MEDDDBASE, seleon GmbH and partners will offer invaluable insights to streamline your entry into the European market. Learn from the best about: ✅ Navigating regulatory approvals ✅ Streamlining partnerships for smooth market entry ✅ Real-world case studies for success 🎤 Introducing seleon GmbH's speakers: Peter Hartung, Dr. Annette von der Groeben, René Schmidt, Anne Matousek, Julian Alpers, Jörg Hauffe and Fabiola Hartung-Linz. With over 26 years of expertise, seleon delivers end-to-end development, consulting, and production services for medical devices. Gain valuable insights into navigating Europe’s dynamic market from their extensive experience. 📅 Date: Wednesday, October 30 🕘 Times: 9:00 AM & 5:00 PM CET 🔗 Register here: https://lnkd.in/ecqUPPWB #MedicalDevices #MarketEntry #regulatoryaffairs #mdr #Webinar #Europe

📣 Save The Date!     Lebon Aymeric , Medtech Commercial Director at PLG will host 2 speaking sessions at MEDICA - Leading International Trade Fair: ·       (Slot 1) 📅 12 November | 15:15 – 15:45 📍 German Pavilion Stage Topic: Developing an Effective Regulatory Strategy: Securing a Seamless IVDR Transition Aligned with Your Business Objectives (for non-IVD, jRUO, IVD products) ·      (Slot 2) 📅 13 November | 15:30 – 16:30 📍 German Pavilion Stage Topic: Clinical Validation for Software Integrating AI Do not miss your chance to connect and be part of these sessions where we will cover essential and emerging challenges in the Medtech industry, offering valuable insights into both regulatory strategy and clinical validation for AI-driven software. From 11 – 14 November, meet ProductLife Group at the German Pavilion, C80, Hall 3. 📲 Connect now on MEDICA match-making app to secure meetings with our team: Pascale Cousin, Lebon Aymeric, Keval Bhoola, Vincent L. and Fernando Mayoral Alonso. #ProductLifeGroup #MEDICA #Dusseldorf #MedicalDevices #IVDR #ClinicalValidation #RegulatoryStrategy #AIinHealthcare #MedicalSoftware #GlobalHealthcare #LifeSciences #GermanPavilion #MedTech #HealthcareInnovation

🚀 Cyclops Medtech: Revolutionizing Balance & Dizziness Diagnostics! 🌟 Balance and dizziness disorders are more than just an inconvenience—they're a global health issue that affects millions, often severely impacting daily life, mobility, and well-being. But despite their prevalence, diagnosing the root causes of these conditions can be complicated, leading to delays in treatment and frequent misdiagnoses. That’s where Cyclops Medtech steps in. Introducing BalanceEye VOG—a game-changing, CE Class 2A certified Video-Oculography (VOG/VNG) system that's transforming how healthcare professionals diagnose and manage vestibular disorders. This innovative technology offers precise, reliable assessments of inner ear and brain function, providing clinicians with the data they need for faster, more accurate diagnoses of balance and dizziness conditions. ✅ Faster diagnoses. ✅ Personalized treatment plans. ✅ Better patient outcomes. Cyclops Medtech is on a mission to empower clinicians with the tools they need to provide exceptional patient care and improve the quality of life for those affected by vestibular dysfunction. Reach out today to learn more about how BalanceEye VOG can support your practice and enhance patient care. #CyclopsMedtech #Balance #Dizziness #VestibularHealth #VOG #VNG #InnovativeHealthcare #PatientCare #MedTech #HealthTech #MedicalInnovation #HealthcareRevolution

Welcome to Week 40 of 52 Weeks of WOW: Word of the Week Wednesdays Word of the Week: ATTENDEE REGISTRATION Attendee Registration: The pivotal process through which individuals sign up to participate in a conference, typically requiring the submission of personal and professional details. Why is this important? Attendee registration serves as the gateway to the conference, enabling organizers to manage logistics, allocate resources, and tailor the event experience to the needs and preferences of registered attendees. What does the planner need to do? Develop user-friendly registration platforms, establish clear registration policies and procedures, and provide prompt and responsive support to registrants to ensure a seamless registration experience. How can planners apply it? By implementing efficient and accessible registration systems, planners can streamline the registration process, maximize attendee engagement, and gather valuable data to inform event planning and management. Key takeaway: Attendee registration is the first step towards a successful conference experience, laying the groundwork for attendee engagement, networking, and knowledge exchange within the conference community. #52WeeksofWOW #MEDiC #MEDiCseries #pharma #biotech #medicalmeetings #mmp #eventsindustry #meetingsandevents #eventprofs #medcomms #medicalcommunications

✨ MEDICA 2024 HIGHLIGHTS A massive thank you to everyone I had the chance to meet at the show—hope you enjoyed the Stroopwafels! 😄🍪 Over two productive days at #MEDICA and #COMPAMED, I had the pleasure of: ✅ Catching up with 8 incredible clients ✅ Engaging in 22 insightful conversations about European expansion ✅ Connecting with 6 of our valued networking partners Looking forward to continued connections & discussions! 🚀 #europe #eurodev #businessdevelopment

Exciting News from Accorto Regulatory Solutions! We are thrilled to announce our participation in four major events over the next few weeks: 📍 San Diego, CA - BIO24 This week, our team is in sunny San Diego attending the BIO International Convention, one of the most significant biotech events of the year. Anders Horn and Jasmine Birlew, MS are looking forward to engaging with industry leaders, exploring innovative technologies, and sharing their expertise in regulatory solutions. 📍 Dubai, UAE - Global Vape Forum Next up, our Chief Science Officer Vincent Angelico will be taking the stage not once, but twice at the Global Vape Forum in Dubai from June 14-16. This is an incredible opportunity to discuss the latest trends, regulations, and scientific advancements in the nicotine industry. Don't miss our sessions! 📍 Miami, FL - FIME & Next Generation Nicotine Finally, we'll be heading to Miami for not one, but two exciting events! Anders Horn and Kristina Haysmer will be attending FIME, one of America's leading medical device tradeshows. Join us as we connect with professionals from around the globe, showcase our regulatory solutions, and explore groundbreaking medical technologies. Simultaneously, Vincent Angelico will be across town at Next Generation Nicotine Delivery where he will be in discussions with industry partners and stakeholders on challenges in the industry and the evolving regulatory landscape. We can't wait to connect with you at these events! If you're attending any of these, please reach out and let's schedule a time to meet. See you there! 🌐🤝 #AccortoRegulatorySolutions #BIO24 #GlobalVapeForum #FIME #Biotech #VapingIndustry #MedicalDevices #RegulatoryExcellence #Innovation #Networking

Fuel Your Clinical #RFP with #SuperNOVA at #BIOAsia24 Do you have an upcoming #clinicaltrial or #clinicaltrialsimaging needs?Would you like to explore different options for clinical trials and imaging needs? If so, please reach out to us to discuss your #RFP needs. We will also be exhibiting at #BIOAsia24 at the end of July 24. Elevate your clinical research journey with the SuperNOVA 40 oz thermal cup—the ultimate companion for busy professionals navigating the industry's demands. This high-performance insulated cup keeps your hot beverages piping hot for up to 12 hours and your cold drinks refreshingly chilled for up to 24 hours, ensuring you stay energized and focused throughout the conference and beyond. As a special offer, SuperNOVA Clinical Research is giving away a limited number of these coveted cups to the first 8-12 organizations that engage with us during the upcoming BIO Asia 24 conference and initiate RFP discussions. This is your chance to not only secure a practical and stylish accessory but also to explore the transformative clinical solutions that SuperNOVA has to offer. Don't miss out on this exclusive opportunity to fuel your clinical breakthrough. Schedule a meeting with our team at the conference and let's discuss how SuperNOVA's innovative technologies, patient-centric approaches, and global expertise can propel your clinical trials to new heights of success. Secure your free SuperNOVA 40 oz cup and start your path to clinical innovation today. #ClinicalResearch #CRO #PharmaceuticalIndustry #BiotechIndustry #ClinicalTrials #PatientCentricity #ThermalCup #FreeGiveaway #ConferenceOffer #InnovativeSolutions #GlobalExpertise #RegulatoryCompliance #ImagingServices #RFPDiscussions

🔈 Last week I had the pleasure to attend as a member of Amadix to the third edition of Team PRRC annual summit in Malaga.💡As important take home messages, we can highlight: 🔹The PRRC should not only ensure compliance with the MDR/IVDR, but also with all legislation applicable to medical devices, such as the new IA Act. 🔹Work must be done on the implementation of the IA Act in combination with the IVDR/MDR. 🔹In audits, Notified Bodies (NBs) or Competent Authorities expect that the intervention and action of the PRRC in critical regulatory activities will be reflected in the Quality System documentation. 🔹SMEs are facing difficulties in the transition to IVDR in relation to the associated costs and lack of experience with NBs, especially for IVD SMEs. 🔹Manufacturers need more specification from NBs on what they expect to receive to demonstrate compliance with requirements. This can be achieved through structured dialogues with NBs. 🔹Concern is expressed about the innovation blockade in Europe and the lack of a dedicated pathway for innovative products, such as the Breakthrough Device Program at the FDA. 🔹In Switzerland, they are working towards recognition of FDA approval to ensure, among other things, that the Swedish population has access to innovative medical devices. 🔹UK will update its medical device regulation more closely resembling the IVDR/MDR. I would like to thank AseBio - Asociación Española de Bioempresas for giving me the opportunity to attend, and TEAM-PRRC for organising the event which has allowed us to learn more about the key role that PRRC plays within a company, as well as creating an ideal environment for the exchange of experiences and knowledge between the actors in this sector, being very valuable. #TeamPRRC #IVDR #Compliance