Veeva Systems APAC’s Post

🌟 Just one week to go: DIA Core Singapore Annual Meeting 2024 🌟 🗓️ Save the Date: July 16, 17 2024 📍 Location: Singapore This event promises to be a cornerstone for professionals in the healthcare, pharmaceutical, and regulatory sectors. Whether you're looking to network with industry leaders, gain insights into the latest innovations, or contribute to pivotal discussions shaping the future of healthcare, DIA Core Singapore 2024 is the place to be. The program committee put together a comprehensive program from keynote addresses by industry pioneers to interactive workshops and panel discussions, the program promises to be insightful and forward-thinking. Finny Liu Sannie SF Chong Jack Wong 🚀(Asia Regulatory Professionals Association) Martin Lim Senthil Sockalingam Innovative Sessions: Engage with thought-provoking sessions on regulatory updates, clinical trials, patient engagement, and more. Networking Opportunities: Connect with peers, mentors, and potential collaborators from around the globe. Expert Speakers: Learn from Health Authority representatives and industry experts. Don't miss out on this exceptional opportunity to be part of the conversation shaping the future of Healthcare in Asia.🌍💡 #HealthcareInnovation #Pharmaceuticals #RegulatoryAffairs #DIA2024 #SingaporeEvents https://lnkd.in/evWxxptc

Join us for an insightful #webinar as we explore strategies for optimizing clinical supply management and mastering the EU Qualified Person release process! Topic: Key Accesses to Multinational Clinical Studies Success: Optimized Clinical Supply Management and EU Qualified Person Release Process Date: April 17, 2024 Time: 2:30 PM - 4:00 PM (SGT) Don't miss out on valuable insights and strategies to ensure success in multinational #clinical studies. Register now: https://lnkd.in/dJzUMUvj Catalent Pharma Solutions Serena Yu Johannes Hirt Rebecca Fan #clinicalsupplychain #clinicaltrials #EUQP #multinationalstudies #clinicalresearchmanagement #globalclinicaltrials #supplychainoptimization #EUregulations #clinicaloperations #clinicallogistics

Our article "The Dynamics of Field Medical Visits: Importance of Balancing Quality and Frequency in Medical Interactions" has been published on PHARMA JAPAN, thanks to their kind collaboration with Trilations! This is based on an extensive analysis of 45,000 interactions, we reveal key strategies to help you refine your approach and achieve greater impact. PHARMA JAPAN is a subscription based page in Japan. Please reach out to Joeri De Haes, Leen Helsloot or our team in Japan Shinichi Yoshino, Hanna Sumida, MBA to me if you have any queries or would like to discuss more about this topic. Thanks Lukas Van der Donckt for the contributions! Trilations Healthcare Strategies #MAF, #medicalaffairs, #medical, #MSL

Dive into the operational changes biopharma companies are making to comply with the EU Clinical Trials Regulation (EU CTR). Novo Nordisk shares their approach to overcoming operational challenges, including: • Coordinating cross-functional submissions • Aligning EU CTR protocols with global study standards • Integrating new operational methodologies into a complex organizational framework Stay ahead of the regulatory curve and gain valuable industry insights. See the complete article here: https://lnkd.in/gAVifWG2

Is your clinical trial process 𝘀𝘁𝘂𝗰𝗸 𝗶𝗻 𝗻𝗲𝘂𝘁𝗿𝗮𝗹? It's time to 𝗮𝗰𝗰𝗲𝗹𝗲𝗿𝗮𝘁𝗲. 𝗥𝗲𝘃𝗮𝗺𝗽 𝗬𝗼𝘂𝗿 𝗖𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗧𝗿𝗶𝗮𝗹𝘀 𝘄𝗶𝘁𝗵 𝗜𝗤𝗩𝗜𝗔 𝗜𝗻𝗻𝗼𝘃𝗮𝘁𝗶𝗼𝗻 𝗗𝗮𝘆 𝗮𝘁 𝗦𝗖𝗢𝗣𝗘 𝗘𝘂𝗿𝗼𝗽𝗲 2024𝗅 Join us at the 𝗜𝗤𝗩𝗜𝗔 𝗜𝗻𝗻𝗼𝘃𝗮𝘁𝗶𝗼𝗻 𝗗𝗮𝘆 𝗮𝘁 𝗦𝗖𝗢𝗣𝗘 𝗘𝘂𝗿𝗼𝗽𝗲 2024 for a complimentary afternoon of game-changing insights and solutions. 𝗛𝗲𝗿𝗲'𝘀 𝘄𝗵𝗮𝘁 𝗮𝘄𝗮𝗶𝘁𝘀 𝘆𝗼𝘂: 𝗖𝘂𝘁𝘁𝗶𝗻𝗴-𝗘𝗱𝗴𝗲 𝗜𝗻𝘀𝗶𝗴𝗵𝘁𝘀: Get a glimpse into the future of clinical research with presentations from IQVIA's digital product leaders. 𝗜𝗻𝘁𝗲𝗿𝗮𝗰𝘁𝗶𝘃𝗲 𝗗𝗲𝗺𝗼𝘀: Experience firsthand how IQVIA's innovative technologies can streamline your workflows, improve patient engagement, and boost site efficiency. 𝗢𝗽𝗲𝗻 𝗗𝗶𝘀𝗰𝘂𝘀𝘀𝗶𝗼𝗻: Challenge industry experts with your questions and learn from the experiences of your peers at the "𝗜𝗻𝗻𝗼𝘃𝗮𝘁𝗶𝗼𝗻 𝗙𝗼𝗿𝘂𝗺." 𝗡𝗲𝘁𝘄𝗼𝗿𝗸𝗶𝗻𝗴 𝗢𝗽𝗽𝗼𝗿𝘁𝘂𝗻𝗶𝘁𝗶𝗲𝘀: Connect with other clinical trial professionals, build meaningful relationships, and explore potential collaborations. 𝗧𝗵𝗶𝘀 𝗲𝘃𝗲𝗻𝘁 𝗶𝘀 𝗶𝗱𝗲𝗮𝗹 𝗳𝗼𝗿: Pharmaceutical executives Trial managers Medical directors Business operations professionals Patient or site engagement specialists Strategic sourcing leads Register today for IQVIA Innovation Day at SCOPE Europe 2024: https://lnkd.in/gqA9ZnwB #IQVIAInnovationDay #SCOPEEurope #ClinicalTrials #Innovation #ClinicalOperations #Networking

As this new chapter for Europe begins, all eyes will be on the top priorities for parliament for the months and years ahead. The review of the #EUPharmaPackage will be high on the list, and rightly so. This offers a once in a generation opportunity to ensure that Europe remains at the forefront of biomedical innovation. It's vital that the final text EU decision-makers will need to agree on, help to establish a more resilient system, where regulations keep pace with scientific progress and facilitate innovations that address unmet needs, are accessible across the EU, and improve patient outcomes. With its new mandate in place, I look forward to seeing new and returning Members of the European Parliament come together with the EU Commission and Member States to ensure the new pharmaceutical framework facilitates innovation and unlocks tomorrow's cures for patients.

🔔 𝗧𝗵𝗲 𝗘𝘂𝗿𝗼𝗽𝗲𝗮𝗻 𝗠𝗲𝗱𝗶𝗰𝗶𝗻𝗲𝘀 𝗔𝗴𝗲𝗻𝗰𝘆 (𝗘𝗠𝗔), 𝗶𝗻 𝗰𝗼𝗹𝗹𝗮𝗯𝗼𝗿𝗮𝘁𝗶𝗼𝗻 𝘄𝗶𝘁𝗵 𝘁𝗵𝗲 𝗛𝗲𝗮𝗱𝘀 𝗼𝗳 𝗠𝗲𝗱𝗶𝗰𝗶𝗻𝗲𝘀 𝗔𝗴𝗲𝗻𝗰𝗶𝗲𝘀 (𝗛𝗠𝗔) 𝗮𝗻𝗱 𝘁𝗵𝗲 𝗘𝘂𝗿𝗼𝗽𝗲𝗮𝗻 𝗖𝗼𝗺𝗺𝗶𝘀𝘀𝗶𝗼𝗻 (𝗘𝗖), 𝗵𝗮𝘀 𝗹𝗮𝘂𝗻𝗰𝗵𝗲𝗱 𝘁𝘄𝗼 𝗮𝗱𝘃𝗶𝗰𝗲 𝗽𝗶𝗹𝗼𝘁𝘀 𝘂𝗻𝗱𝗲𝗿 𝘁𝗵𝗲 𝗔𝗰𝗰𝗲𝗹𝗲𝗿𝗮𝘁𝗶𝗻𝗴 𝗖𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗧𝗿𝗶𝗮𝗹𝘀 𝗶𝗻 𝘁𝗵𝗲 𝗘𝗨 (𝗔𝗖𝗧 𝗘𝗨) 𝗶𝗻𝗶𝘁𝗶𝗮𝘁𝗶𝘃𝗲. These pilots aim to improve clinical trial applications by offering scientific and regulatory advice. The first pilot provides joint scientific advice on marketing authorisation and clinical trial applications, while the second offers technical and regulatory support before trial submission. These initiatives seek to enhance application quality and streamline the clinical trial process in Europe. https://lnkd.in/dvzt9kWA

Want to immediately know the latest events in EU pharma? Our new dashboard is going to help everyone to do that! See immediate summaries of the previous weeks: - New parallel trade licenses granted (European and national) - New tenders launched across Europe - New clinical trials launched globally - Notes added by other colleagues in your company account - New shortage announcements Exciting to be combining all this data together into a single location, and finding new business for our clients.

The role of data is changing in #pharma - and it’s a topic that needs to be discussed. I love how #VeevaSummit brings the industry together to connect and exchange ideas on important topics like this. For the Compass and OpenData keynote, I’ll be joined on stage by three incredible biopharma leaders - Mike Rifflard of ANI Pharmaceuticals, Inc., Patrick Moeller of Bayer, and Matt Winkler of Takeda Oncology.   This is one you won’t want to miss.

The upcoming Clinical Trial Supply Europe 2024 conference will gather pharma and biotech delegates to discuss the trends and challenges in the clinical trial supply industry, where pharmaceutical companies and biotech’s will discuss and debate new technologies and processes aimed at streamlining supply chain operations, over the course of two days.