Rephine’s Post

As day 1 of CPHI gets ready to kick-off and you're building your agenda, don't forget to attend this valuable session by Charles Gibbons: ✨ Deep Dive: Navigating Data Compliance Standards in Pharma ✨ Tuesday, October 8, 2024 3:45 PM to 4:10 PM · 25 min. (local time) ✨ Hall 5 - 5B49 ✨ Manufacturing 5.0 Pharma thrives on innovation but requires strict regulations for safe and effective drugs. In today's age, navigating compliance for complex new technologies, drug manufacturing and patient safety adds to the challenge. 📣 Learn more about: - How compliance management systems such as digital documentation can reduce errors and enhance consistency processes. - What does efficient auditing look like and how to achieve it. - Insights into efforts towards regulatory harmonization and its impact on international manufacturing and market access. #dataintegrity #digitalisation #pharma #regulatoryaffairs #compliance #quality #qms #digital #Milan 📣 Can't make it to the session or have other questions? We have a team on site along with Charlie, including Michele Sinoway, ready to meet with you. Just send us a message and we can find a time to get together!

India is the pharmacy to the world, including the US. I am looking forward to this discussion on US #drugshortages, policy and implications for Indian industry. #uspmedicinesupplymap

🌟 We're thrilled to announce the release of our new partner catalog on our website! 🚀 Discover the strategic collaborations that enhance our expertise and enhance our scope of action in the healthcare sector. 💼 We're proud to partner with well-known collaborators to deliver cutting-edge solutions in medical devices, in vitro diagnostics and pharmaceuticals. 🤝 Here's a glimpse of our partners and the benefits of our collaborations: MD101: Comprehensive solutions to expedite the development and market access of medical devices while adhering to regulatory standards. Euris: Secure healthcare data management to ensure regulatory compliance and patient confidentiality. LABY by KYLI: Advanced software solutions for research and development, accelerating medical discoveries. Easy-CRF SAS: Powerful tools to simplify clinical data collection and analysis for effective and precise studies. Global Regulatory Partners, Inc. Partners: Comprehensive support for regulatory compliance to navigate a complex regulatory landscape. Medone Research: Strengthening the quality and efficiency of clinical trials to obtain valuable product data. Cerebellis: Software development expertise and tailored consulting for solutions that meet the specific needs of medical device companies. Haempharma (Pty) Ltd: Facilitated access to the healthcare market in Southern Africa, ensuring regulatory compliance and efficient product distribution. Medicen Paris Region: assistance with calls for projects. Eurobiomed: assistance with calls for projects. Explore our catalog attached to learn more about our partners and the innovative solutions we offer together! 💡 If you want more details, don’t hesitate to contact us at customer.service@med-clinical.fr or visit us at www.medclinical.fr  #Partnerships #HealthcareInnovation #MedicalDevices #InVitroDiagnostics #pharmaceuticals #collaboration #catalog #expertise #regulatory #compliance #confidentiality #discoveries #data #patientcare #marketaceess #clinicaltrials

Our panellist at our #Pharma #AntiCounterfeiting, #Serialisation & #SupplyChain Security 2024 will be Steven Ustel, Jyrki Syvaeri, Jonathan Buisson, Vineet Khanna, Cameron McKinnell, Demet Tazegul https://lnkd.in/gjprg46v For our upcoming conferences visit : https://lnkd.in/gjQY86dn Fen Castro Piyush Patel #VIpsscs #VIpasscs #trackandtrace #traceability #supplychainsecurity #brandprotection #anticounterfeit #vipacs #Counterfeit #manufacturing #logistics #OperationAncord #lascarancord #ancord #packaging #smartpackaging #packaginginnovation #pharmalabelling #artwork #pharmalabels #scm #Healthcare #TrackTrace #drugs #medicines #Anticounterfeiting #Drugregulatory #Pharmaceuticals #clinicaltrials #clinicalresearch #Qualitycontrol #RegulatoryAffairs #pharmanews #regulatory #pharmaceuticalindustry #biotech 

Meet Nextrove, LLC, our newly joined Exhibitor for the 2024 edition of World Drug Safety Congress Americas. Keep reading to learn about our exhibitor and how to meet their team face-to-face ⬇️ Nextrove, LLC is a systems agnostic global Lifesciences Systems Integrator, focusing exclusively on delivering Pharmaceutical and Biotech solutions. They take pride in being the only niche consulting firm to assist clients with Pharmacovigilance, Hosting, eTMF, RIM, Regulatory Affairs and Clinical Operations, Medical Information, Artificial Intelligence, Salesforce, and Integration services. Their mission is to deliver preeminent and innovative solutions that enable the global Health Science industry to improve public and patient safety. 🌎 Nextrove has a global team with established offices in New Jersey, Milan, Tokyo, Shanghai, Bangalore, Chennai, and Noida. With over 20+ years’ experience, they help our clients meet their global digitalization strategy, maintain regulatory compliance, and drastically reduce the total cost of ownership in a variety of engagements. The combination of their business knowledge and technical skill set allows them to bridge the gap between business needs and technology to meet and exceed the expectations of their clients. 🙌 Learn more about Nextrove and their services offered this fall. 𝗚𝗲𝘁 𝘆𝗼𝘂𝗿 𝘁𝗶𝗰𝗸𝗲𝘁 𝘁𝗼𝗱𝗮𝘆 𝘁𝗼 𝗺𝗲𝗲𝘁 𝘁𝗵𝗲𝗺 𝗶𝗻-𝗽𝗲𝗿𝘀𝗼𝗻 𝗼𝗻 𝗼𝘂𝗿 𝗲𝘅𝗽𝗼 𝗳𝗹𝗼𝗼𝗿: https://lnkd.in/gqpN6izz #WorldDrugSafety #pharmacovigilance #drugsafety #biotechsolutions #regulatoryaddiars #clinicaloperations #medicalinformation #patientsafety #publicsafety

Are you considering launching your medicinal product in the Nordics? Our head of Market Access, Susanne Schuurman will be at #CPHIMilan, representing Arex Advisor. She will take you through the benefits of our Contract Pharma Organisation concept. At Arex Advisor we are passionate about helping leaders and companies secure access for new treatments in Europe, and especially in the Nordics and BeNeLux. We have specific experience in collaborating with authorities and other relevant stakeholders. Our local market intelligence will help you make the right decision for your product. How can combined expertise in Market Access and Regulatory Affairs improve your business case? Let’s connect and find out! To book a meeting, send a note in the partnering system, or to contact@arexadvisor.com. Looking forward to seeing you there! #Arexadvisor #marketaccess #regulatoryaffairs #pharmabusiness #reimbursement #geoexpansion #commercialization #CPHI #launch

In today’s complex pharmaceutical landscape, hosting events that are both compliant and impactful requires more than just coordination - it requires expertise. Here’s why outsourcing your event management can be a game-changer. As a pharmaceutical event specialist, I manage everything from compliance with stringent industry regulations to integrating scientific insights with audience engagement tactics. Internal teams often face resource constraints. Partnering with an expert optimises budgets by ensuring every detail, from vendor negotiation to logistical execution, aligns with your goals. With over 25 years of experience, I bring a proven track record to mitigate risks and ensure that every event aspect runs smoothly, allowing your in-house team to focus on core responsibilities. Wondering how outsourcing your events for 2025 could work for you, Let’s have a chat ☕ #eventprofs #pharmaevents #SMA #events #eventmanagement

Check out how you can improve your Nordic business case!

Day 1 at #CPhI has been filled with engaging discussions. From evaluating CDMO capabilities to discussing strategic expansion, it's been a day rich in opportunities and connections. Kiirsten Suurkask Steve King Alain Suurkask Reach out to learn more about the following opportunities: 🏭 GMP-compliant biomanufacturing sites? Let's talk about what's available in the US, European, and LATAM markets. 🛠️ State-of-the-art facilities? Learn more about a US-based sterile fill-finish operation offering advanced solutions. 🧪 API production? We've got insights on sites in Western Europe and the US. 👁️💧 Looking for cutting-edge production in ophthalmics, semi-solids, and liquids? Ask about a new site in LATAM. ❄️🏢 Need for GMP warehousing and cold storage solutions? Let's connect. #Manufacturing #PharmaIndustry #Biotech #Networking #GMP #Innovation

❗Last chance to register! Join us tomorrow in this insightful webinar to explore the latest developments in the EU medical device vigilance landscape, with industry-renowned specialist Veronika Valdova. Learn how to seamlessly integrate medical devices into your pharma portfolio, gain practical strategies for navigating regulations, and establish robust management processes. 📅 Tomorrow, 17 April. Choose the time that best suits you: 🕚 Session 1: 6am ET | 12pm CET 🕚 Session 2: 10am ET | 4pm CET 🕚 Session 3: 2pm ET | 8pm CET 👉 Register here: https://lnkd.in/e9q4cqRa 🔍 Key topics include: • Introduction to Medical Device Regulatory Requirements • Addressing Practical Challenges • Key Takeaways • Q&A Session 🎯 This webinar is ideal for: • MedTech company leaders in acquisition by pharma • Pharma company leaders expanding their portfolio to include device products. For any questions about this webinar, or if you would like to request the recording, please write to: contact@qinecsa.com. See you soon! #Pharmacovigilance #MedicalDevices #EURegulations #PharmaDevices #MedicalDeviceRegulation #PharmaPortfolio #Webinar #Qinecsa