Pharmacovigilance USA Congress #Boston’s Post

Excited to be in London next month for the 11th Annual Outsourcing in Clinical Trials UK and Ireland 2024 Conference! Find Emma Cullen and Méline Rostain at Booth #2 as they look forward to networking face to face, hearing from the expert speaker line-up, and discussing the latest innovations, regulatory updates, and opportunities within the clinical trial landscape. Outsourcing in Clinical Trials Event Series #OCTUK #OCTIreland #ClinicalTrials #Healthcare #Pharma #ClinicalOperations #BioPharma #BioTech #LifeSciences #Regulatory #ClinicalResearch #AI

We're thrilled to announce our participation at the prestigious 6th Annual Life Science Regulatory Intelligence & Strategy Conference, happening this week in Baltimore, MD, USA. Stop by the Celegence booth to connect with industry experts Sonia A. Veluchamy, Lakshmeenarayana Goundalkar (LGG), and Marloes van Bruggen - van der Geer. Let's ignite discussions, foster collaboration, and share invaluable insights into the ever-evolving pharmaceutical regulatory landscape. 🕥 𝗕𝘂𝘁 𝘄𝗮𝗶𝘁, 𝘁𝗵𝗲𝗿𝗲'𝘀 𝗺𝗼𝗿𝗲! Prepare to embark on an insightful journey into Regulatory Intelligence with our esteemed Head of Regulatory Affairs, Marloes van der Geer. Join her at 10:45 AM CT for an engaging panel discussion on "𝗣𝗿𝗮𝗰𝘁𝗶𝗰𝗮𝗹 𝗦𝘁𝗿𝗮𝘁𝗲𝗴𝗶𝗲𝘀 𝘁𝗼 𝗕𝘂𝗶𝗹𝗱 𝗮 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗜𝗻𝘁𝗲𝗹𝗹𝗶𝗴𝗲𝗻𝗰𝗲 𝗚𝗿𝗼𝘂𝗽 𝗳𝗿𝗼𝗺 𝗦𝗰𝗿𝗮𝘁𝗰𝗵." Want to find out more? Drop us a line at info@celegence.com to connect! #regulatoryintelligence #regulations #healthcare #lifesciences #regulatorycompliance #regulatorystrategy #compliance  

#PharmacovigilanceOctobers at Cloudbyz #WDSC Europe could not have come at a better time! Having successfully completed the setup of our PV database for a major sponsor in Europe and putting finishing touches to our new version of the Cloudbyz PV package, due for release shortly, we are more excited than ever to talk about your PV reporting challenges and explore how we can help in resolving them. If you are visiting, please don't forget to swing by Booth 41 tomorrow to discuss how Cloudbyz can help enhance your SAE reporting process!

🌟 Key Speaker Announcement!🌟  We are honoured to welcome Dr. Khaudeja Bano, Vice President of Combination Product, Devices, Diagnostics, and Software as a Medical Device Quality at Amgen, as a #Key Speaker at Pharmacovigilance Europe 2025! 🎤 Dr. Bano’s extensive expertise in #medicaldevice quality and combination products makes her an invaluable addition to our lineup. She will be sharing insights on the latest developments and quality standards in device and diagnostic safety—a must-attend session for all Pharma and Biotech professionals. 📅 Join us in London on 21-22 May 2025 to learn from Dr. Bano and other global leaders in pharmacovigilance. #Pharmacovigilance2025 #KeySpeaker #PVAudits #REMS #DrugSafety #Pharma #Biotech #LondonConference #PVEurope #PharmaLeaders #worlddrugsafety #ClinicalSafety #patientsafety #RiskManagement #clinicaltrials #clinicalresearch #pv #pharma #healthcare #lifesciences #RegulatoryAffairs #RegulatoryWriting #MedicalWriting #scientificwriting #wdsc #wdscboston #regulatory #medicinesaffairs #pharmaceuticals #biosimilars #biotech #patientcentric #vigilance #pharmaceuticalindustry

We are excited to share that our Chief Scientific Officer, Hans van Bruggen, recently presented at a 3-day event hosted by TOPRA - The Organisation for Professionals in Regulatory Affairs. The attendees were immersed in a wealth of information and insights, guided by inspiring presenters. Hans emphasized the practical and strategic aspects of global #regulatoryaffairs, helping attendees develop sufficient knowledge and skills to provide advice to their companies and contribute to #regulatory strategy. The event highlighted that regulatory affairs is not black and white but full of nuances where every answer depends on the perspective taken. The training was led by 𝐈𝐧𝐞𝐤𝐞 𝐉𝐨𝐧𝐤𝐞𝐫-𝐇𝐨𝐨𝐠𝐞𝐫𝐤𝐚𝐦𝐩 and Hans, supported by multiple experts lecturing during the course. Attendees gained valuable skills in asking the right questions to derive well-balanced and justified answers. 🔗 Explore the course details and see when the next session is scheduled: https://lnkd.in/g9gaaZUp #pharma #pharmaceuticals #regulatorycourse #TOPRA #biotech #regulatorystrategy #regulatorycompliance #regulatoryprocedure

Ready to dive into the world of drug development? 💊 Join us for an insightful online workshop on "Regulatory Considerations in Pre-Clinical Drug Development" led by our Fábio Pereira Lampreia, PhD, and organized by CoLAB AccelBio. Whether you're a beginner or seeking to expand your expertise, this session is ideal for you. 🗓️ Date: September 18th ⏰ Time: 3 PM 💻 Where: Online 🎟️ Register here: https://lnkd.in/dN3h_Squ Free, but mandatory. Don't miss this opportunity to stay ahead in your field. Secure your spot now!!! #DrugDevelopment #RegulatoryAffairs #PreClinicalResearch #ColabTrials #Workshop #BiomedicalResearch

Our CEO, Alan White, is travelling to the DIA 2024 Global Annual Meeting in San Diego. *** Visiting between June 17-19th during the event. *** DIA (Drug Information Association) is a premier forum for the life sciences community, and Alan is eager to connect with industry leaders, regulators, and innovators who share our passion for the pharma biotech sector. Are you attending DIA 2024? We'd love to schedule a meeting with Alan to discuss the future and how we can advise, help, or collaborate. Please direct message @Arriello or Alan White directly if you’d like to say hi in California. And...stay tuned or connect with Alan for more updates throughout the conference! #DIA2024 #pharmaceuticals #regulatory #pharmacovigilance #quality

Are you ready for Europe’s new #pharma rules? Ahead of the European Elections, Europe’s pharmaceutical and life sciences sector is undergoing major changes – with far-reaching implications for its life sciences ecosystem. As new regulations are set to reshape the industry, companies have the unique opportunity to advocate for #innovation and #competitiveness in the sector. Our healthcare experts outline what’s at stake, and what businesses can expect from the new rules. Read more here: https://ow.ly/o65W50RcHPF

As the excitement builds for the World Drug Safety Congress Americas in #Boston, industry leaders and experts are gearing up for a day filled with cutting-edge discussions and networking opportunities. Set against the backdrop of one of America’s foremost medical hubs, this year’s congress promises to be a pivotal event for professionals in the pharmaceutical and biotech sectors. Our team is looking forward to discussions on the latest trends, challenges, and technologies shaping the future of our field. We invite you to visit our booth (#327) and learn more about how Orbis Clinical is committed to delivering high-quality services that support your drug safety needs. Let’s collaborate to ensure that patient safety remains a top priority in our industry. Jessica Leveille, Melissa Douglas, Ryan Jacklin Terrapinn World Drug Safety Congress Americas Orbis Clinical #worlddrugsafety #DrugSafetyUS #lifescience #businessdevelopment #staffing #recruiting #safety #talent #consultants #pharmaceuticalindustry #biotech #resource #drugsafety #conference #Boston #pharmacovigilance

Hello connections! ✨ I'm thrilled to share that I've completed the Good Clinical Practices (GCP) training program by the National Institute on Drug Abuse (NIDA) This comprehensive training has enhanced my understanding of clinical research ethics, regulations, and best practices. I'm now better equipped to contribute to high-quality, compliant, and patient-centered research studies. 🧬 🦠 Thanks to NIDA for providing this valuable resource! 🎉 #GCP #ClinicalResearch #NIDA #GoodClinicalPractices #ResearchExcellence #ClinicalTrials #Healthcare #Pharmaceuticals #Biotechnology #MedicalResearch