Pharma Focus Europe

08/01/2026

𝐍𝐚𝐧𝐨𝐦𝐞𝐝𝐢𝐜𝐢𝐧𝐞𝐬 are changing how modern therapies are developed—but manufacturing consistency is key.

In Pharma Focus Europe Magazine – Issue 07, Mark van Eldijk (Ardena) shares how flow manufacturing helps overcome scalability and quality challenges in nanoparticle production.

A must-read for pharma professionals working on next-generation drug delivery and advanced therapeutics.

𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐭𝐡𝐞 𝐞-𝐛𝐨𝐨𝐤 𝐧𝐨𝐰 𝐨𝐧 𝐨𝐮𝐫 𝐰𝐞𝐛𝐬𝐢𝐭𝐞: https://www.pharmafocuseurope.com/magazine

𝐑𝐞𝐚𝐝 𝐭𝐡𝐞 𝐚𝐫𝐭𝐢𝐜𝐥𝐞: https://www.pharmafocuseurope.com/manufacturing/translating-nanomedicine-potential-into-a-scalable

07/01/2026

Advanced therapies like biologics, mRNA, and nanoparticle-based medicines face major stability challenges—but lyophilisation is changing the game.

In Pharma Focus Europe Issue 07, Uwe Hanenberg (Recipharm) shares expert insights on how lyophilisation improves shelf life, supports sustainable distribution, and enables scalable manufacturing for complex therapeutics.

𝐑𝐞𝐚𝐝 𝐭𝐡𝐞 𝐚𝐫𝐭𝐢𝐜𝐥𝐞: https://www.pharmafocuseurope.com/manufacturing/lyophilisation-key-to-overcoming-stability

𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐭𝐡𝐞 𝐞-𝐛𝐨𝐨𝐤 𝐧𝐨𝐰:
https://www.pharmafocuseurope.com/manufacturing/lyophilisation-key-to-overcoming-stability

06/01/2026

𝐐𝐮𝐚𝐥𝐢𝐭𝐲, 𝐜𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐜𝐞, 𝐚𝐧𝐝 𝐝𝐢𝐠𝐢𝐭𝐚𝐥 𝐦𝐚𝐭𝐮𝐫𝐢𝐭𝐲 are no longer optional in pharma and medtech manufacturing.

The 𝐌𝐚𝐬𝐭𝐞𝐫 𝐂𝐨𝐧𝐭𝐫𝐨𝐥 𝟑-𝐢𝐧-𝟏 𝐆𝐮𝐢𝐝𝐞 covers:
✔️ A complete guide to pharmaceutical quality management
✔️ Key ways modern MES solutions improve manufacturing efficiency
✔️ A clear view of digital maturity across pharma and medtech operations

A valuable resource for teams navigating regulatory pressure and digital change.

👉 𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐲𝐨𝐮𝐫 𝐜𝐨𝐩𝐲 𝐧𝐨𝐰: https://www.pharmafocuseurope.com/promotion/master-control-pharma-manufacturing-resources

Quality isn’t exclusive to a single department. It’s all-pervasive and integral to every function throughout the enterprise. Despite the inherent challenges of connecting quality and compliance data in an industry defined by truncated timelines, greater product complexity and personalization, an...

06/01/2026

Clinical trial delays often start at site activation.

In the latest 𝐏𝐡𝐚𝐫𝐦𝐚 𝐅𝐨𝐜𝐮𝐬 𝐄𝐮𝐫𝐨𝐩𝐞 𝐦𝐚𝐠𝐚𝐳𝐢𝐧𝐞 (𝐈𝐬𝐬𝐮𝐞 𝟎𝟕), 𝐌𝐞𝐥𝐢𝐬𝐬𝐚 𝐇𝐮𝐭𝐜𝐡𝐞𝐧𝐬 𝐚𝐧𝐝 𝐆𝐚𝐫 𝐂𝐫𝐨𝐰𝐞𝐥𝐥 (𝐖𝐂𝐆) share data-driven insights on how improving site initiation cadence can significantly reduce enrollment timelines in Phase III oncology trials.

📉 Faster site activation = quicker patient enrollment + lower operational costs
📘 Backed by advanced ML-based predictive analytics

👉 𝐕𝐢𝐬𝐢𝐭 𝐨𝐮𝐫 𝐰𝐞𝐛𝐬𝐢𝐭𝐞 𝐭𝐨 𝐫𝐞𝐚𝐝 𝐭𝐡𝐞 𝐚𝐫𝐭𝐢𝐜𝐥𝐞: https://www.pharmafocuseurope.com/clinical-trials/optimising-clinical-trial-start-

𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐭𝐡𝐞 𝐞-𝐛𝐨𝐨𝐤: https://www.pharmafocuseurope.com/magazine

05/01/2026

𝐒𝐮𝐬𝐭𝐚𝐢𝐧𝐚𝐛𝐢𝐥𝐢𝐭𝐲 is becoming a core pillar of pharmaceutical manufacturing. 🌍💊

Eco-friendly practices like energy-efficient production, reduced waste, green chemistry, and sustainable packaging are helping pharma companies lower costs, meet regulatory demands, and strengthen brand trust.

👉 𝐑𝐞𝐚𝐝 𝐭𝐡𝐞 𝐟𝐮𝐥𝐥 𝐢𝐧𝐬𝐢𝐠𝐡𝐭𝐬 𝐨𝐧 𝐬𝐮𝐬𝐭𝐚𝐢𝐧𝐚𝐛𝐥𝐞 𝐩𝐡𝐚𝐫𝐦𝐚 𝐦𝐚𝐧𝐮𝐟𝐚𝐜𝐭𝐮𝐫𝐢𝐧𝐠:
https://www.pharmafocuseurope.com/articles/sustainable-pharma-manufacturing-eco-friendly-practices

05/01/2026

𝐒𝐞𝐜𝐮𝐫𝐢𝐧𝐠 𝐜𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐭𝐫𝐢𝐚𝐥 𝐝𝐚𝐭𝐚 is critical to patient safety, compliance, and scientific credibility. Blockchain technology is now playing a key role in ensuring tamper-proof, transparent trial records.

Authored by Debasish Kar, Senior Clinical Project Coordinator, Thermo Fisher Scientific. Featured in Pharma Focus Europe – Issue 07

𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐭𝐡𝐞 𝐞-𝐛𝐨𝐨𝐤: https://www.pharmafocuseurope.com/magazine

𝐑𝐞𝐚𝐝 𝐡𝐨𝐰 𝐛𝐥𝐨𝐜𝐤𝐜𝐡𝐚𝐢𝐧 𝐬𝐭𝐫𝐞𝐧𝐠𝐭𝐡𝐞𝐧𝐬 𝐭𝐫𝐮𝐬𝐭 𝐢𝐧 𝐜𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐫𝐞𝐬𝐞𝐚𝐫𝐜𝐡
https://www.pharmafocuseurope.com/clinical-trials/blockchain-in-securing-clinical-trial-data

03/01/2026

𝐈𝐧-𝐯𝐢𝐯𝐨 𝐂𝐀𝐑-𝐓 𝐭𝐡𝐞𝐫𝐚𝐩𝐲 could change how cell therapies are developed, delivered, and scaled—bringing faster treatment and broader patient access.

Featured in Pharma Focus Europe Magazine – Issue 07, Peter Robinson, MBA, Director of Therapeutic Strategy at Novotech, shares expert insights on the science, clinical progress, and regulatory pathways shaping the “Age of In-Vivo” CAR-T.

𝐑𝐞𝐚𝐝 𝐭𝐡𝐞 𝐚𝐫𝐭𝐢𝐜𝐥𝐞: https://www.pharmafocuseurope.com/research-development/in-vivo-car-t-from-concept-to-clinic

𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐭𝐡𝐞 𝐞-𝐛𝐨𝐨𝐤 𝐭𝐨𝐝𝐚𝐲 𝐨𝐧 𝐨𝐮𝐫 𝐰𝐞𝐛𝐬𝐢𝐭𝐞: https://www.pharmafocuseurope.com/magazine

02/01/2026

Quality, efficiency, and digital readiness are critical priorities for today’s pharmaceutical and medtech manufacturers.

𝐓𝐡𝐞 𝐌𝐚𝐬𝐭𝐞𝐫 𝐂𝐨𝐧𝐭𝐫𝐨𝐥 𝟑-𝐢𝐧-𝟏 𝐆𝐮𝐢𝐝𝐞 𝐜𝐨𝐦𝐛𝐢𝐧𝐞𝐬 𝐭𝐡𝐫𝐞𝐞 𝐞𝐬𝐬𝐞𝐧𝐭𝐢𝐚𝐥 𝐫𝐞𝐬𝐨𝐮𝐫𝐜𝐞𝐬 𝐢𝐧𝐭𝐨 𝐨𝐧𝐞:
• Pharmaceutical Quality Management best practices
• How modern MES solutions streamline manufacturing
• Building digital maturity across pharma and medtech operations

Designed for professionals focused on compliance, operational excellence, and future-ready manufacturing.

𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐲𝐨𝐮𝐫 𝐜𝐨𝐩𝐲 𝐧𝐨𝐰:
https://www.pharmafocuseurope.com/promotion/master-control-pharma-manufacturing-resources

Quality isn’t exclusive to a single department. It’s all-pervasive and integral to every function throughout the enterprise. Despite the inherent challenges of connecting quality and compliance data in an industry defined by truncated timelines, greater product complexity and personalization, an...

02/01/2026

Reactive stability testing is costing the pharmaceutical industry millions.

In Pharma Focus Europe—Issue 07, Sneha Chauhan, Senior Product Development Specialist, Multisorb Filtration Group, explains how a 𝐩𝐫𝐨𝐚𝐜𝐭𝐢𝐯𝐞, 𝐬𝐜𝐢𝐞𝐧𝐜𝐞-𝐥𝐞𝐝 𝐬𝐭𝐚𝐛𝐢𝐥𝐢𝐭𝐲 𝐬𝐭𝐫𝐚𝐭𝐞𝐠𝐲 can help manufacturers prevent degradation risks before they impact patients or profits.

From hydrolysis and oxidation to QbD-led packaging decisions, this article outlines a smarter path to long-term product quality.

𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐭𝐡𝐞 𝐞-𝐛𝐨𝐨𝐤: https://www.pharmafocuseurope.com/magazine

𝐑𝐞𝐚𝐝 𝐭𝐡𝐞 𝐜𝐨𝐦𝐩𝐥𝐞𝐭𝐞 𝐚𝐫𝐭𝐢𝐜𝐥𝐞: https://www.pharmafocuseurope.com/strategy/from-reactive-to-proactive

31/12/2025

𝐏𝐡𝐚𝐫𝐦𝐚𝐜𝐞𝐮𝐭𝐢𝐜𝐚𝐥 𝐪𝐮𝐚𝐥𝐢𝐭𝐲 is entering a new era—where algorithms, audits, and human judgment intersect.

The latest article in Pharma Focus Europe Magazine (Issue 07) by Akshay Peer (TrakCel) and Dr. Sophie Fröhlich (Takeda) looks at how digital transformation is improving compliance, accelerating approvals, and reshaping quality roles across pharma.

A must-read for quality, regulatory, and manufacturing leaders.

👉 𝐑𝐞𝐚𝐝 𝐦𝐨𝐫𝐞: https://www.pharmafocuseurope.com/magazine

𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐭𝐡𝐞 𝐞-𝐛𝐨𝐨𝐤 𝐟𝐫𝐨𝐦 𝐨𝐮𝐫 𝐰𝐞𝐛𝐬𝐢𝐭𝐞:
https://www.pharmafocuseurope.com/magazine

30/12/2025

The shift to 𝐩𝐚𝐩𝐞𝐫𝐥𝐞𝐬𝐬 𝐩𝐡𝐚𝐫𝐦𝐚 𝐦𝐚𝐧𝐮𝐟𝐚𝐜𝐭𝐮𝐫𝐢𝐧𝐠 is redefining efficiency, compliance, and quality. Integrated digital systems help manufacturers reduce errors, accelerate batch release, and stay inspection-ready at all times.

Learn how full digital maturity can transform pharma production operations.

👉 𝐕𝐢𝐬𝐢𝐭 𝐨𝐮𝐫 𝐰𝐞𝐛𝐬𝐢𝐭𝐞 𝐭𝐨 𝐫𝐞𝐚𝐝 𝐭𝐡𝐞 𝐜𝐨𝐦𝐩𝐥𝐞𝐭𝐞 𝐚𝐫𝐭𝐢𝐜𝐥𝐞
https://www.pharmafocuseurope.com/articles/digital-maturity-pharma-manufacturing-paperless-guide

30/12/2025

Strong quality systems, efficient MES tools, and a clear digital roadmap are essential for the future of pharma and medtech.

Our 𝐌𝐚𝐬𝐭𝐞𝐫 𝐂𝐨𝐧𝐭𝐫𝐨𝐥 𝟑-𝐢𝐧-𝟏 𝐆𝐮𝐢𝐝𝐞 brings all of this together in one powerful resource!
✔ Pharmaceutical Quality Management
✔ Modern MES Solutions
✔ Digital Maturity in Pharma & Medtech

Get practical insights to enhance compliance, efficiency, and operational excellence.

𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐲𝐨𝐮𝐫 𝐜𝐨𝐩𝐲 𝐧𝐨𝐰: https://www.pharmafocuseurope.com/promotion/master-control-pharma-manufacturing-resources

Quality isn’t exclusive to a single department. It’s all-pervasive and integral to every function throughout the enterprise. Despite the inherent challenges of connecting quality and compliance data in an industry defined by truncated timelines, greater product complexity and personalization, an...