Innovative Cell Therapy CDMO Solutions

Our Capabilities

Bringing Your Cell & Gene Therapy Products to the Market

We commit to delivering the highest-quality contract development and manufacturing services to our partners

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cGMP iPSC Development

Pioneers in cGMP iPSCs

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Process & Analytical Development

Begin with the end in mind

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Manufacturing Science & Technology

A comprehensive approach to technology transfer

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Clinical & Commercial Manufacturing

Delivering innovative, life-changing cell therapies

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Quality & Regulatory Compliance

A holistic innovative approach to quality

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Supply Chain & Logistics

Managing logistics with patients in mind

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Success Powered by Cutting-Edge Science

RoslinCT, as one of the first in the world to produce clinical-grade human pluripotent stem cells, has a strong focus on science and innovation. In collaboration with our partners, RoslinCT is supporting the development and future commercialization of cell therapies based on a broad range of cell types with an advanced program utilizing CRISPR-edited stem cell-based therapy.

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200 +

cGMP Batches Produced

for various indications

22 +

cGMP Suites

allowing simultaneous processing

350 +

Experienced Employees

across two continents

20 +

Cell Types

experience supporting auto and allo processes

Purpose-Built cGMP Manufacturing Facilities

Benefit from our world-class, innovative cell therapy development and cGMP manufacturing facilities

RoslinCT Boston Facility

RoslinCT Edinburgh Facility

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RoslinCT Boston Operations Center

cGMP Manufacturing

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About RoslinCT

Get to Know the Team and What We Stand for

Innovative Solutions. Trusted Partnerships. Life-changing Treatments.

Following the world-breaking first cloning of a mammal (Dolly the Sheep) at the Roslin Institute within the University of Edinburgh (UK) in 1997, there was worldwide interest to access Roslin’s technology and expertise. RoslinCT was established in 2006 to translate this cutting-edge science and apply it to the development of human medicines.

To save the lives of patients by empowering our partners to efficiently progress cell & gene therapies from development to commercialization, as their advanced CDMO partner of choice.

We are a team of passionate professionals with decades of experience in the advanced cell & gene therapy industry.

The Scientific Advisory Board is comprised of cell and gene therapy pioneers with extensive domain experience.

Deep Scientific Expertise and Diversity of Cell Platform Experience
The One of First in the World to Produce Clinical-Grade Human Pluripotent Cells
Supporting the First CRISPR-Edited Stem Cell-Based Therapy for a Major Disease Currently Pending Marketing Authorization
Process and Analytical Development Laboratory
Clinical and Commercial Manufacturing Capacity
Integration of Best-in-Class Cell Therapy Software Solutions
Extensive Training
Adaptive Approach to Partner Relationships