RoslinCT
RoslinCT is a transatlantic cell and gene therapy CDMO headquartered in Edinburgh, operating 22 cGMP suites in the UK and US to provide process development, manufacturing, and commercial supply for autologous, allogeneic, gene-edited, and iPSC-based therapies for biotech and pharma clients.
- Company typePrivate
- Founded2006
- HeadquartersEdinburgh, United Kingdom
- Headcount251–500
- GTM typeB2B
- OfferingServices
What RoslinCT does
RoslinCT is a UK-headquartered, transatlantic contract development and manufacturing organization (CDMO) specializing in advanced cell and gene therapies, including autologous and allogeneic cell therapies, gene-edited therapies, and induced pluripotent stem cell (iPSC)-based therapies. Founded in 2006 as a spin-out from the University of Edinburgh's Roslin Institute — the birthplace of Dolly the Sheep — the company provides end-to-end services spanning process and analytical development, cGMP cell banking, manufacturing science and technology transfer, clinical and commercial manufacturing, quality and regulatory compliance, supply chain and logistics, and a training academy. Its scientific credentials include being one of the first organizations globally to produce clinical-grade human iPSCs and manufacturing exa-cel (Casgevy), the world's first FDA-approved CRISPR-edited cell therapy for sickle cell disease and transfusion-dependent beta thalassemia, in collaboration with Vertex Pharmaceuticals.
The company operates 22 purpose-built cGMP cell therapy processing suites across two sites — Edinburgh, Scotland (headquarters, 40,000 sq ft, 8 suites) and Hopkinton, Massachusetts (64,000 sq ft, 14 suites, acquired via the 2022 merger with Lykan Bioscience). It is a private, PE-backed entity majority-owned by GHO Capital Partners with WindRose Health Investors retaining a board-level position. RoslinCT employs approximately 300 staff (with the website claiming 500+) and has produced more than 500 cGMP batches supporting 20+ cell types.
Revenue is generated through fee-for-service CDMO contracts — project-based, clinical-stage, and commercial-scale manufacturing agreements with biotech and pharma therapy developers. The commercial-manufacturing portfolio includes exa-cel (for Vertex) and Omisirge (for Ayrmid Pharma/Gamida Cell), with recent additions including a Phase III manufacturing partnership with BOOST Pharma for BT-101. GTM is enterprise field sales with dedicated business development teams covering UK/Europe and the US, leveraging direct outreach, industry conferences, and inbound inquiries. Pricing is not publicly disclosed and is project/quote-based.
RoslinCT firmographics
Firmographics- Name
- RoslinCT
- Legal name
- RoslinCT is a trading name of Roslin Cell Therapies Limited and RoslinCT US Holdings LLC
- Website
- https://roslinct.com
- Company type
- Private
- Founded year
- 2006
- Operating status
- Operating
- Headcount range
- 251–500 employees
- Short description
- RoslinCT is a transatlantic cell and gene therapy CDMO headquartered in Edinburgh, operating 22 cGMP suites in the UK and US to provide process development, manufacturing, and commercial supply for autologous, allogeneic, gene-edited, and iPSC-based therapies for biotech and pharma clients.
- Ownership category
- akta.pro rank
RoslinCT industry classification
Industry- Product category
- Cell Therapy Contract Manufacturing (CDMO)
- NAICS
- Research and Development in the Physical, Engineering, and Life Sciences (54171), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
- SIC
- Services-Commercial Physical & Biological Research (8731)
- akta.pro primary industry
- Cell Therapy CDMO (HLAGABAD)
- akta.pro secondary industries
- Gene Therapy (Viral Vector/Plasmid) CDMO (HLAGABAE), Cell Banking & Viral Seed Services (MCB/WCB/VSB) (HLAGAGAD), Clinical Trial Material (CTM) Manufacturing & Supply CDMO (HLAGABAK)
Keywords
Where RoslinCT is headquartered
LocationHeadquarters
- HQ city
- Edinburgh
- HQ country
- United Kingdom
- HQ region
- Europe
Offices2 records
Markets served
RoslinCT business model
Business model- GTM type
- B2B
- Offering type
- Services
- Cost components
- Personnel, Operations, Infrastructure, Technology or R&D, Marketing or Sales, Supply Chain
Revenue model
- Contract Development and Manufacturing Services: RoslinCT generates revenue by providing fee-for-service CDMO solutions including process development, analytical development, cGMP clinical and commercial manufacturing, and technology transfer services for cell and gene therapy companies. Revenue is earned through project-based contracts, service agreements, and long-term manufacturing partnerships with therapy developers. The company supports both autologous and allogeneic cell therapies and iPSC-based programs across various phases from preclinical through commercial launch.
Go-to-market motion1 record
Distribution channels1 record
Marketing channels6 records
RoslinCT product offering
Product offeringCore offering
RoslinCT is a global Contract Development and Manufacturing Organization (CDMO) specializing in advanced cell and gene therapies. The company provides end-to-end cGMP manufacturing services including process and analytical development, cell banking, iPSC development, gene editing, clinical and commercial manufacturing, and supply chain/logistics, supporting both autologous and allogeneic therapies from early development through commercialization.
Product overview
RoslinCT is an advanced cell and gene therapy Contract Development and Manufacturing Organization (CDMO) offering an integrated platform of services from early development through commercialization. The core platform consists of cGMP iPSC Development (pioneering pluripotent stem cell capabilities), Process & Analytical Development, cGMP Cell Banking, Manufacturing Science & Technology, Clinical & Commercial Manufacturing, Quality & Regulatory Compliance, and Supply Chain & Logistics, all supported by a Training Academy. RoslinCT has manufactured commercial products including exa-cel (the world's first CRISPR-edited cell therapy for Vertex Pharmaceuticals) and Omisirge (FDA-approved cell therapy for Ayrmid/Gamida Cell). The company supports both autologous and allogeneic cell therapy manufacturing through 22 purpose-built cGMP suites across Edinburgh, Scotland and Hopkinton, Massachusetts.
Differentiator
Problem solved
Functional benefit
Products and services
- cGMP iPSC Development
Quantifiable outcome
- 500+ cGMP batches produced for various indications
- +3 more outcomes
Companies that use RoslinCT
Customer profileNamed customers3 records
Segments1 record
Ideal customer profiles2 records
RoslinCT technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature7 records
RoslinCT partnerships and signals
Strategic signalPartnerships
Three partnerships are on record, tiered major and flagship.
- BOOST PharmamajorRoslinCT entered a strategic manufacturing partnership with BOOST Pharma to support Phase III development of BT-101, an allogeneic mesenchymal stem cell therapy for Osteogenesis Imperfecta (brittle bone disease) in infants. BOOST Pharma transferred its manufacturing process to RoslinCT's Edinburgh facilities. The partnership includes end-to-end CDMO support for starting materials and clinical drug product, with a long-term view toward commercial manufacturing. BOOST Pharma was founded on science from Karolinska Institutet and is supported by Industrifonden, Sound Bioventures, and Karolinska Development.
- Ayrmid Pharma Ltd. / Gamida CellmajorRoslinCT and Ayrmid Pharma Ltd. entered into a strategic partnership for the technology transfer and commercial manufacturing of Omisirge (omidubicel-onlv), an FDA-approved nicotinamide-modified allogeneic hematopoietic progenitor cell therapy for hematologic malignancies. Manufacturing is being performed at RoslinCT's Hopkinton, MA facility. The partnership was later expanded in December 2025 to include manufacturing for Omisirge's second FDA-approved indication in severe aplastic anemia (SAA). Ayrmid acquired Gamida Cell, the original developer of Omisirge.
- Vertex PharmaceuticalsflagshipIn collaboration with Vertex Pharmaceuticals, RoslinCT developed, from early process development through commercialization, the first CRISPR-edited cell therapy product (exa-cel / exagamglogene autotemcel / Casgevy) for the treatment of sickle cell disease and transfusion-dependent beta thalassemia. This represents the world's first CRISPR gene editing therapy to receive regulatory approvals (UK, US, EU, Bahrain, Saudi Arabia, Canada) and is priced at approximately $2.2 million per patient.
Scale indicators8 records
Recent moves8 records
Expansion highlights4 records
RoslinCT competitors and assessment
Company assessmentEmerging players
- Cellares: Emerging cell therapy manufacturing automation company offering Cell Shuttle platform for automated, scalable cell therapy manufacturing. Comparable as a cell therapy manufacturing services provider, though focused on automation versus traditional CDMO service model.
- Kincell Bio: Cell therapy development and manufacturing CDMO focused on autologous and allogeneic therapies. Comparable as a specialized cell therapy CDMO with similar customer base; Jessica Carmen, RoslinCT's CCO, previously served as VP of Business Development at Kincell Bio.
Direct peers
- Aldevron (Danaher): Specialized CDMO for plasmid DNA, mRNA, proteins, and gene editing enzymes serving cell and gene therapy developers. Acquired by Danaher for $9.6B in 2021; comparable as a specialized CDMO serving cell/gene therapy market (Michael Chambers co-founded Aldevron and sits on RoslinCT SAB).
- Oxford Biomedica: UK-based cell and gene therapy CDMO specializing in viral vector and cell therapy manufacturing. Comparable as a transatlantic-focused advanced therapy CDMO serving similar biopharma customers with similar cell/gene therapy manufacturing capabilities.
- ReciBioPharm: Cell and gene therapy CDMO offering viral vector and nucleic acid manufacturing services. Directly comparable as a specialized advanced therapy CDMO serving similar biotech customers; Dean Morris, RoslinCT's US COO, joined from ReciBioPharm.
- Cellistic: iPSC-based cell therapy CDMO focused on allogeneic iPSC-derived cell therapy manufacturing. Closely comparable as a specialist cell therapy CDMO with iPSC capabilities serving similar therapy developer customers.
- 3P Biopharmaceuticals: Spanish-based biologics and cell therapy CDMO with process development and GMP manufacturing capabilities. Comparable as a specialized biologics/cell therapy CDMO serving biopharma customers; Alexandra Brownfield, RoslinCT's Head of BD, previously served as Head of BD at 3P Biopharmaceuticals.
Broad incumbents
- Lonza Cell & Gene Technologies: Global CDMO leader with significant cell and gene therapy manufacturing capabilities including the acquired PharmaCell business. Directly comparable as a cell therapy CDMO serving similar biopharma clients but at much larger scale and broader service portfolio.
- Catalent (Novo Holdings): Major global CDMO with cell therapy manufacturing capabilities as part of broader biologics and drug delivery portfolio. Comparable as a CDMO serving biopharma, but with substantially larger scale and integrated services.
- Charles River Laboratories: Large CRO/CDMO with cell therapy manufacturing services (CDMO division). Comparable as a contract manufacturer serving biopharma, but with much broader portfolio including preclinical research, biologics, and discovery services.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat5 records
Key risks6 records
Key highlights7 records
Customer concentration
RoslinCT compliance and trust
Trust signalCompliance1 record
RoslinCT financial estimates
Financial estimateRevenue estimate
Valuation estimate
RoslinCT leadership team
Management profileNumber of profiles
Profiles36 records
RoslinCT subsidiaries and ownership
Company hierarchySubsidiaries1 record
RoslinCT funding detail
Funding detailFunding overview
Funding rounds2 records
Investors2 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
RoslinCT M&A and investment
M&A and investmentM&A1 record
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about RoslinCT
What does RoslinCT do?
RoslinCT is a global Contract Development and Manufacturing Organization (CDMO) specializing in advanced cell and gene therapies. The company provides end-to-end cGMP manufacturing services including process and analytical development, cell banking, iPSC development, gene editing, clinical and commercial manufacturing, and supply chain/logistics, supporting both autologous and allogeneic therapies from early development through commercialization.
Is RoslinCT a public or private company?
RoslinCT is a private company. It is classified as private equity controlled and is currently operating.
When was RoslinCT founded?
RoslinCT was founded in 2006. It employs 251 to 500 people.
Where is RoslinCT based?
RoslinCT is headquartered in Edinburgh, United Kingdom, in the Europe region.
How does RoslinCT make money?
One revenue line is on record: contract Development and Manufacturing Services.
Who are RoslinCT's main competitors?
Emerging players on record are Cellares and Kincell Bio. Direct peers are Aldevron (Danaher), Oxford Biomedica, ReciBioPharm, Cellistic and 3P Biopharmaceuticals. Broad incumbents are Lonza Cell & Gene Technologies, Catalent (Novo Holdings) and Charles River Laboratories.
Does RoslinCT have an API?
No public API is recorded for RoslinCT.
What industry is RoslinCT in?
RoslinCT's product category is Cell Therapy Contract Manufacturing (CDMO). Its primary akta.pro industry code is HLAGABAD, Cell Therapy CDMO, with a secondary code of HLAGABAE, Gene Therapy (Viral Vector/Plasmid) CDMO. Its NAICS code is 54171 and its SIC code is 8731.