Appsilon

Learn how to generate audit-ready validation evidence for R packages for FDA and EMA submissions using a fast, repeatable, risk-based process. Appsilon is hosting a 60-minute webinar The Future of R Package Validation in Regulated Pharma, focused on a practical, risk-based approach to validating both in-house R code and open-source dependencies. 🔗 https://lnkd.in/dBi-ajp2 What you will take away: 1. What FDA and EMA typically expect for reproducibility, traceability, and control 2. How leaders validate third-party packages using risk assessment frameworks 3. How to set up ownership across biometrics, platform engineering, and QA without creating a bottleneck If you are responsible for submissions, clinical reporting pipelines, or validated platforms, this session will help you move faster without re-validation chaos every time the environment changes.

As we reach the end of 2025, we want to express our heartfelt thanks to everyone who was part of our journey this year. It was a year full of challenges - and also a year of growth, learning, and shared responsibility. None of this would have been possible without the dedication of our team, the openness of our partners, and the trust of our clients around the world. To our Appsilon team: thank you for your ownership, kindness, and commitment to excellence - even when things were complex or uncertain. To our clients and partners: thank you for your trust and collaboration. Working together is how meaningful impact happens. We know this season is marked in different ways around the world. Whether you are celebrating holidays now, later, or not at all - we hope this moment brings you joy, rest, reflection, and renewed optimism. Thank you for the work we’ve done together - with care, courage, and high standards. Now, let’s enjoy a well-deserved break and come back ready to keep building what matters - together.

📍Live from PHUSE EU Connect 2025 in Hamburg Jakub Sobolewski talked how to modernize clinical study reporting through automation and modular design. A standout example of collaboration driving excellence in pharma analytics. If you're at PHUSE, come say hi - we're at booth 34 :)

A quick reminder that we’re at PHUSE EU Connect 2025 in Hamburg. Don’t miss out on these two great sessions highlighting how collaboration and modern development practices are reshaping pharma analytics: 💡 Talk: JazzAIR: Advancing Clinical Study Reporting Through Modern Development Practices and Testing Strategy with Jazz Pharmaceuticals & Jakub Sobolewski 🧩 Workshop: Interactive Data Visualization Using the Teal Framework with Peyman Eshghi & André Veríssimo, PhD (full agenda: https://lnkd.in/dwn8ET4i) From automated testing in clinical reporting to hands-on Teal applications, these sessions explore how rigorous engineering and transparent visualisation can accelerate insight delivery while maintaining high quality and regulatory alignment. 📍 Hamburg — November 16–19, 2025 A great opportunity to exchange ideas on advancing excellence in clinical research. Find us at booth 34 (and around the venue).

We’re on our way to PHUSE EU Connect 2025 in Hamburg — and we’re excited to highlight two sessions with the community. If you want to learn how collaboration and modern development practices are reshaping pharma analytics, don't miss out! 💡 Talk: JazzAIR: Advancing Clinical Study Reporting Through Modern Development Practices and Testing Strategy with Jazz Pharmaceuticals & Jakub Sobolewski 🧩 Workshop: Interactive Data Visualization Using the Teal Framework with Peyman Eshghi & André Veríssimo, PhD (full agenda here: https://lnkd.in/dwn8ET4i) From automated testing in clinical reporting to hands-on Teal applications, these sessions explore how rigorous engineering and transparent visualisation can accelerate insight delivery while maintaining high quality and regulatory alignment. 📍 Join us in Hamburg, November 16–19, 2025, to exchange ideas on advancing excellence in clinical research.

How are pharma leaders leveraging GenAI to build better clinical applications faster? If you want to know, join the PHUSE Working Group event today. Appsilon’s Head of Technology, Marcin Dubel, will share our perspective on "GenAI-driven Creation of Clinical Trial Applications". This session explores how Generative AI is transforming the creation of clinical trial tools and making them more accessible, intuitive, and decision-ready within the Teal framework. 📅 October 10 🕙 10:00–11:00 (EDT) | 16:00–17:00 (CEST) 🔗 Register here: https://lnkd.in/d643-Wxx → Join this industry conversation to hear practical insights from leading pharma innovators.

Can GenAI take the Teal framework to the next level in pharma? We think so and we’re ready to show how. Appsilon’s Head of Technology, Marcin Dubel, will join Mahesh Umbarkar, Mike Briganti, Freeman W. and Paweł Rucki at PHUSE’s Working Group event to share our approach to genAI-driven Creation of Clinical Trial Applications. It’s a session for anyone thinking critically about speed, usability, and impact in clinical tools. 📅 October 10 ⏰ 10:00–11:00 EDT | 16:00–17:00 CEST 🎙️ Practical use cases, real challenges, and bold ideas

Our Head of Technology - Marcin Dubel - will present how GenAI is enabling interactive, instant creation of clinical trial applications with the power of Teal. Don't miss out and register for the PHUSE Working Group event. 📍 What to expect: - How GenAI improves the efficiency and usability of Teal dashboards - Ways pharma teams are accelerating development cycles - Lessons from real-world applications 📆 October 10 ⏰ 10:00–11:00 (EDT) / 16:00–17:00 (CEST) 🔗 Register here: https://lnkd.in/d643-Wxx Don't miss it if you’re working on digital transformation or trial analytics in pharma.

BioTechX Europe 2025 kicks off its 10th anniversary edition today, bringing together biotech, pharma, and data science leaders for three days of high-impact conversations. With a packed agenda on AI in drug development, multiomics, and precision medicine, Iwona Matyjaszek and Karolina Jabłońska of team Appsilon are eager to exchange ideas and bring back the best of what’s next. With momentum already building on Day 1, we’re looking forward to learning, sharing, and connecting with partners pushing the future of data-driven pharma. If you're at the event too — let's chat 👋

Faster clinical reporting starts with a modern, compliant Statistical Computing Environment (SCE) — modular, cloud-ready, validated, and built to support SAS, R, Python, and the tools of tomorrow. What does the future SCE look like? In our special live episode, experts from Jazz Pharmaceuticals (Megan L. Dunham), Novo Nordisk (Andrew York), and Appsilon (Rafael Pereira) discuss: ⬡ Key elements of a compliant, modern SCE ⬡ Implementation best practices and pitfalls to avoid ⬡ Real-world success stories ✦ Watch the full conversation here: https://lnkd.in/dTAZ66Ud ✦ Dive deeper with our free ebook: https://lnkd.in/d_dPSV6n