PrimeVigilance ’s Post

Exciting First Day at the Conference! We’re thrilled to be here at Farma Forum 2024 and already had some great conversations on pharmacovigilance, clinical safety, and regulatory compliance. If you’re attending, don’t miss the opportunity to stop by our booth G31 at Hall 9! Whether you're looking for expert support on PV audits, Pharmacovigilance services, clinical safety for sponsors of clinical trials, or simply to expand your network, we’d love to chat and explore how PVpharm can help you meet your goals. Let’s connect and discuss how we can assist with your pharmacovigilance needs. See you soon! #Farmaforum #pharmacovigilance

Pharmacovigilance is crucial for detecting, assessing, understanding, and preventing adverse effects of medicines. Join us to explore key topics including legislative and corporate governance requirements, the management of adverse events in clinical trials and post-approval, and how the risk-benefit profile of a product evolves. You'll gain insights into the cross-functional role of pharmacovigilance and its interaction with stakeholders. Our upcoming course 'An Introduction to Pharmacovigilance', will provide a comprehensive understanding of its importance throughout the drug development process and product lifecycle. We will also cover the Australian and international legislative frameworks that guide pharmacovigilance practices, and the processes for collecting, documenting, assessing, and reporting adverse events. Learn how this data helps update reference safety information. 𝗗𝗼𝗻’𝘁 𝗺𝗶𝘀𝘀 𝗼𝘂𝘁 𝘁𝗵𝗲 𝗲𝗮𝗿𝗹𝘆 𝗯𝗶𝗿𝗱 𝘀𝗽𝗲𝗰𝗶𝗮𝗹 — 𝘀𝗮𝘃𝗲 $𝟰𝟬𝟬+ 𝗯𝘆 𝗿𝗲𝗴𝗶𝘀𝘁𝗲𝗿𝗶𝗻𝗴 𝘁𝗼𝗱𝗮𝘆 𝗯𝗲𝗳𝗼𝗿𝗲 𝘁𝗵𝗲𝘆 𝗲𝗻𝗱. ➡️ https://bit.ly/4dqYBMF

📅 15th-17th July, 2024 – EARLY BIRD OFFER! Time to save when booking onto our upcoming training course for European Post Marketing Pharmacovigilance! ⬇ https://lnkd.in/erte8YcD This 3-day online course will be led by our CEO Graeme Ladds and hosted by Management Forum Ltd: designed for pharmacovigilance, clinical, QA, and regulatory personnel seeking to further their understanding of new European legislation, covering pharma processes for managing the safety of company’s products, key post-market pharmacovigilance activities, signal analysis, safety communication and much more. Save on multiple bookings when attending with a colleague! - 30% off the 2nd delegate - 40% off the 3rd delegate - 50% off the 4th delegate Book before 10th June and save £300! ⬇ https://lnkd.in/erte8YcD #pharmacovigilance #drugsafety #training #trainingdevelopment #EMA #QPPV #SOP #medicalinformation #medicalaffairs #qualityassurance #compliance #regulatoryaffairs #regulatorycompliance

📌 FREE WEBINAR \- Navigating Local Pharmacovigilance in European countries: Are you meeting all local safety requirements? 📅 September 19  🕒3:00 pm  💻 Online      ▶ Interested in knowing how to define the responsibilities of key PV personnel, including EU QPPVs and local contacts?    🔝 Then do not miss this webinar! Join ASPHALION expert Laura Eder Azanza, PhD. as she shares valuable insights that will help you dive into local pharmacovigilance requirements in Europe with ease and confidence!  🔗 Register here: <https://bit.ly/3y5AvHO> In the meantime, check out our interactive map that shows you just that, local pharmacovigilance requirements in Europe! <https://bit.ly/3Sw3paK>  <https://bit.ly/4da9Vw2>  #Webinar #FreeWebinar #PV #EU #Pharmacovigilance #Vigilance #EURequirements #Europe #LocalPV #LocalPharmacovigilance #MeetTheExpert #RA #RegulatoryAffairs #WeAreAsphalion #WeCare #KnowledgeFromExperience   

📌 FREE WEBINAR | Navigating Local Pharmacovigilance in European countries: Are you meeting all local safety requirements? 📅 September 19  🕒3:00 pm  💻 Online      ▶ How about learning how to navigate country-specific PV requirements to manage the particular PV obligations of each European country?    🔝 Join ASPHALION expert Laura Eder Azanza, PhD. as she shares valuable insights that will help you dive into local pharmacovigilance requirements in Europe with ease and confidence!  🔗 Register here: https://bit.ly/3y5AvHO https://bit.ly/4da9Vw2  #Webinar #FreeWebinar #PV #EU #Pharmacovigilance #Vigilance #EURequirements #Europe #LocalPV #LocalPharmacovigilance #MeetTheExpert #RA #RegulatoryAffairs #WeAreAsphalion #WeCare #KnowledgeFromExperience   

Exploring the Role of the Qualified Person for Pharmacovigilance (QPPV) in the EU! Discover the crucial steps and considerations involved in registering your QPPV and ensuring compliance with regulatory standards. Check out our latest blog post to learn more: https://lnkd.in/grPU4igB At Artixio, we understand the complexities of pharmacovigilance and offer comprehensive solutions to support your regulatory compliance needs. Our expertise spans regulatory affairs, pharmacovigilance, and quality assurance, enabling us to guide you through the registration process seamlessly. With Artixio, you can: 🔹 Access expert guidance on QPPV registration requirements 🔹 Ensure compliance with EU pharmacovigilance regulations 🔹 Receive tailored training for QPPVs and pharmacovigilance personnel 🔹 Stay informed about regulatory updates and best practices Ready to enhance your pharmacovigilance practices and ensure patient safety? Contact us at info@artixio.com to learn more about our services and how we can support your organization. #Pharmacovigilance #RegulatoryCompliance #QPPV #DrugSafety #Artixio #PatientSafety #HealthcareCompliance #EURegulations #LinkedInPost

In this episode, we delve into the crucial role of the Pharmacovigilance Qualified Person (QPPV). We'll explore their responsibilities, qualifications, and the importance of their role in ensuring patient safety. From setting up pharmacovigilance systems to managing risk assessments and responding to regulatory inquiries, the QPPV plays a pivotal role in the post-marketing surveillance of medications. #qppv #pharmacovigilance

🚀𝗦𝘁𝗿𝗲𝗮𝗺𝗹𝗶𝗻𝗲 𝗬𝗼𝘂𝗿 𝗚𝗹𝗼𝗯𝗮𝗹 𝗟𝗶𝘁𝗲𝗿𝗮𝘁𝘂𝗿𝗲 𝗠𝗼𝗻𝗶𝘁𝗼𝗿𝗶𝗻𝗴 𝘄𝗶𝘁𝗵 𝘁𝗵𝗲 𝗗𝗿𝘂𝗴𝗖𝗮𝗿𝗱 𝗣𝗹𝗮𝘁𝗳𝗼𝗿𝗺 Are you involved in global literature monitoring for pharmacovigilance at your company? ✅If you find yourself saying "Yes" to any of these questions, it's time to reach out to us: 1️⃣Is your monitoring process still manual? 2️⃣Are you spending countless hours each week monitoring global literature? 3️⃣Are you feeling burnt out by the workload? You're not alone. Monitoring global medical literature 📚is crucial not just for patient and drug safety but also for meeting regulatory requirements across the entire #pharmacovigilance system. 🔥With the DrugCard platform, we simplify life for pharmacovigilance specialists, ensuring that monitoring global literature is as straightforward as local sources. 🧠Want to learn more? Check out our latest blog post to see how the DrugCard platform streamlines literature monitoring in the #PubMed database: https://lnkd.in/dnNhyd6v #drugsafety #GVP

Missed our webinar? Watch the replay on setting up PV systems in the UK and EU/EEA. Gain crucial insights into QPPV roles, compliance, and drug safety

📅 15th-17th July, 2024 – EARLY BIRD OFFER! Time to save when booking onto our upcoming training course for European Post Marketing Pharmacovigilance! ⬇ https://lnkd.in/erte8YcD This 3-day online course will be led by our CEO Graeme Ladds and hosted by Management Forum Ltd: designed for pharmacovigilance, clinical, QA, and regulatory personnel seeking to further their understanding of new European legislation, covering pharma processes for managing the safety of company’s products, key post-market pharmacovigilance activities, signal analysis, safety communication and much more. Save on multiple bookings when attending with a colleague! - 30% off the 2nd delegate - 40% off the 3rd delegate - 50% off the 4th delegate Book before 10th June and save £300! ⬇ https://lnkd.in/erte8YcD #pharmacovigilance #drugsafety #training #trainingdevelopment #EMA #QPPV #SOP #medicalinformation #medicalaffairs #qualityassurance #compliance #regulatoryaffairs #regulatorycompliance