Software Solution to Automate Cell Therapy Manufacturing Workflows

Software Software Solution to Automate Cell Therapy Manufacturing Workflows

2024-03-14 Source: Press release Thermo Fisher Scientific 1 min Reading Time

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Thermo Fisher Scientific has introduced the Gibco CTS Cellmation Software, the industry’s first off-the-shelf validated software solution to automate cell therapy manufacturing workflows.

Gibco Cell Therapy Systems (CTS) Cellmation Software digitally connects instruments from across Thermo Fisher’s cell therapy portfolio to streamline and automate manufacturing. (Source: Thermo Fisher Scientific) — Gibco Cell Therapy Systems (CTS) Cellmation Software digitally connects instruments from across Thermo Fisher’s cell therapy portfolio to streamline and automate manufacturing.
(Source: Thermo Fisher Scientific)

To optimize clinical manufacturing processes for innovators developing breakthrough cell therapies, Thermo Fisher Scientific recently announced the launch of the Gibco Cell Therapy Systems (CTS) Cellmation Software, a first-of-its-kind automation solution designed to connect and integrate workflows across multiple Thermo Fisher Scientific cell therapy instruments while enabling cGMP compliance. This new offering can help eliminate the need for costly custom software projects and extensive validation, saving valuable time and resources during the cell therapy manufacturing process and helping to deliver these promising curative therapies more quickly and safely to patients, shares the company.

The cell therapy manufacturing process is estimated to include upwards of 40 manual touchpoints, increasing opportunities for errors and contamination that can lead to failure and delay potentially life-saving treatment for those who need it most. The CTS Cellmation Software, powered by Emerson’s Delta V Distributed Control System (DCS), connects Thermo Fisher’s cell therapy instruments within a single, user-friendly interface, reducing the number of manual touchpoints required. By establishing an automated workflow across multiple stages of cell therapy manufacturing, the software enables traceability, repeatability and 21 CFR Part 11 compliance with secured data connectivity, adds the firm.

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