CellPort Software @CellPortSW

Explore our case study featuring Spark Therapeutics and Absorption Systems. See how CellPort supported the potency assay for LUXTURNA, moving it from Process Analytical Development to GMP with flexibility, FDA audit readiness, and compliance. cellportsoftware.com/case-studies/l…

EMA 2025 sets higher standards for data integrity, traceability, and documentation. The FDA’s Transparency Initiative shows that 483s often cite gaps in these same areas. Our blog explores how SaaS platforms provide the digital safety net to address them. cellportsoftware.com/blog/empowerin…

CellPort isn’t just another ELN. Unlike traditional systems, it’s designed for cells—supporting research through GMP with real-time tracking, lineage integrity, and audit-ready records. cellportsoftware.com/blog/eln-featu…

EMA 2025 guidelines raise ATMP expectations—see how a SaaS lab management system like CellPort turns these requirements into daily practice with lineage, traceability, and validated records. cellportsoftware.com/gated/leveragi…

CellPort is attending Advanced Therapies Europe, September 2–4 in Barcelona—bringing together ATMP and regenerative medicine leaders. On Sept 3 at 11:00 AM in Theatre 2, Patrick Dentinger joins “Is decentralised manufacturing the way to cost effectiveness?” See you in Barcelona.

We are excited to be part of Advanced Therapies Europe 2025, September 2–4 in Barcelona. Our CEO, Patrick Dentinger, will join the panel “Is decentralised manufacturing the way to cost effectiveness?” on September 3 at 11:00 AM in Theatre 2. We look forward to connecting!

EMA’s 2025 ATMP guidance calls for full traceability, process control, and validated documentation. Download our white paper to see how SaaS laboratory management systems enable cell lineage tracking, material oversight, and GMP-ready batch records. cellportsoftware.com/gated/leveragi…

New White Paper for Download! Learn how SaaS platforms unify complex ATMP processes—from cell lineage tracking and material traceability to digital batch records and equipment calibration—to help teams align with EMA 2025 guidelines. Download here: cellportsoftware.com/gated/leveragi…

As regulations evolve, SaaS platforms like CellPort empower cell-based labs to keep documentation clear, ensure full traceability, and maintain compliance—helping teams work confidently every day. Read more: cellportsoftware.com/blog/navigatin…

Cells are complex. Your workflows don’t have to be. CellPort brings structure that adapts—connecting inventory, protocols, scheduling, and teams in one intuitive platform. From research to GMP, get visibility, traceability, and control. cellportsoftware.com/blog/cellport-…

Cell-based workflows are complex. Managing them shouldn’t be. See how CellPort connects protocols, batch records, and materials—all in one traceable system. Watch the video: cellportsoftware.com/video/best-eln…

CellPort is at the Process Development for Cell Therapies Summit, July 16–17 in Boston. Join our CEO’s talk, “From Bench to Batch: Operational Readiness for ATMPs in the New Regulatory Era,” July 16 at 11:30 AM. Visit our booth to see how we support cell therapy development!

Join CellPort at the 2025 Philly Cell & Gene Therapy Conference June 27–28. Don’t miss our CEO’s talk, “From Bench to Batch: Operational Readiness for ATMPs in the New Regulatory Era,” June 27 at 11:45 AM. Visit our booth to see how CellPort improves compliance and efficiency.

Traditional systems often fall short for cell-based operations, where precision, traceability, and evolving protocols matter most. Specialized software—like CellPort—provides the tools teams need to stay confident and compliant. Download the white paper: cellportsoftware.com/gated/the-case…

We’re excited to be a part of the Philly Cell & Gene Therapy Conference — June 27–28 in King of Prussia! Don’t miss our talk: “From Bench to Batch: Operational Readiness for ATMPs in the New Regulatory Era”, June 27 at 11:45 AM in the Malvern Room. Visit our booth to connect!

EMA’s 2025 guidelines raise the bar for data integrity & traceability. Specialized software—like CellPort—offers the capabilities needed for audit readiness, traceability, and multi-site control. Download: cellportsoftware.com/gated/the-case…

EMA’s new 2025 guidelines emphasize traceability and documentation in cell-based workflows. CellPort offers digital batch records, real-time tracking, flexible workflows, and audit-ready data to help labs stay compliant and efficient. Learn more: cellportsoftware.com/blog/cellport-…

Working with living cells means managing constant complexity. Our latest white paper explores why traditional systems fall short—and how purpose-built software like CellPort supports cell-based workflows from end to end. Download here: cellportsoftware.com/gated/the-case…