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RoslinCT

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Namestring
RoslinCT
Legal namestring
RoslinCT is a trading name of Roslin Cell Therapies Limited and RoslinCT US Holdings LLC
Websiteurl
roslinct.com
Company typeenum
Private
Founded yearint
2006
Descriptiontext

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.

Short descriptiontext

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.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersEdinburgh, United Kingdom
HQ citystring
Edinburgh
HQ countrystring
United Kingdom
HQ regionstring
Europe
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
cell therapy CDMO, cGMP manufacturing, iPSC development, gene therapy services, contract development manufacturing
Industry4 codes
1Cell Therapy CDMO
CodeHLAGABADPrimaryYes
2Gene Therapy (Viral Vector/Plasmid) CDMO
CodeHLAGABAEPrimaryNo
3Cell Banking & Viral Seed Services (MCB/WCB/VSB)
CodeHLAGAGADPrimaryNo
4Clinical Trial Material (CTM) Manufacturing & Supply CDMO
CodeHLAGABAKPrimaryNo
NAICS code2 codes
  • Research and Development in the Physical, Engineering, and Life Sciences54171
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Cell Therapy Contract Manufacturing (CDMO)
No data
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Contract Development and Manufacturing Services
TypeProfessional Services
Description

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.

roslinct.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Personnel, Operations, Infrastructure, Technology or R&D, Marketing or Sales, Supply Chain
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

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.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 500+ cGMP batches produced for various indications
+3 more records
Product overview1 text field

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.

Product and service1 record
1cGMP iPSC Development
Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2026-01-07
Description

RoslinCT 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.

2Ayrmid Pharma Ltd. / Gamida Cell
Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2025-03-11
Description

RoslinCT 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.

roslinct.com
Strategic tierFlagshipTypeStrategic or Co-development Partner
Description

In 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.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeEmerging player
Description

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.

TypeDirect peer
Description

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).

TypeEmerging player
Description

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.

TypeDirect peer
Description

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.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

TypeDirect peer
Description

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.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment1 record

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles36 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance1 record

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors2 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

RoslinCT

Cell Therapy Contract Manufacturing (CDMO)roslinct.com

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.

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

  • Cell therapy CDMO
  • CGMP manufacturing
  • IPSC development
  • Gene therapy services
  • Contract development manufacturing

Where RoslinCT is headquartered

Location

Headquarters

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

  1. 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 offering

Core 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 profile

Named customers3 records

Segments1 record

Ideal customer profiles2 records

RoslinCT technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature7 records

RoslinCT partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered major and flagship.

  • BOOST PharmamajorStrategic or Co-development Partner · 7 January 2026RoslinCT 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 CellmajorStrategic or Co-development Partner · 11 March 2025RoslinCT 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 PharmaceuticalsflagshipStrategic or Co-development PartnerIn 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 assessment

Emerging 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 signal

Compliance1 record

RoslinCT financial estimates

Financial estimate

Revenue estimate

Valuation estimate

RoslinCT leadership team

Management profile

Number of profiles

Profiles36 records

RoslinCT subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

RoslinCT funding detail

Funding detail

Funding 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 investment

M&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.

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Live signals
Pulse 2.0RoslinCT Awarded Up To £7.25 Million Scottish Enterprise Grant For Digital Cell Therapy ManufacturingRoslinCT received an R&D grant of up to £7.25 million from Scottish Enterprise to accelerate digital transformation of its cell therapy manufacturing operations. The multi-year initiative aims to improve operational efficiency, data connectivity, and manufacturing performance across Scottish operations. The company expects the program to support both clinical and commercial cell therapy production.FinancialContent Business PageRoslinCT Awarded £7.25 million Scottish Enterprise R&D Grant to Advance Digital Cell Therapy ManufacturingRoslinCT received a £7.25 million Scottish Enterprise R&D grant to accelerate digital transformation of its cell therapy manufacturing in Scotland. The funding supports a multi-year initiative to enhance digital and AI capabilities, aiming to improve operational efficiency and strengthen Scotland's position as a global hub for advanced therapies.Longevity.TechnologyBlueRock, RoslinCT partner to expand developer access to stem cell therapiesRoslinCT and BlueRock Therapeutics have entered a strategic partnership to broaden access to BlueRock's clinical-grade induced pluripotent stem cell lines for cell therapy developers. The companies completed a technical transfer of the cell lines to RoslinCT's facilities, enabling RoslinCT to offer cell banking, process development, and GMP manufacturing services alongside its existing capabilities, while BlueRock retains oversight of commercial licensing. The expanded offering is intended to provide developers with a more comprehensive pathway to advance pluripotent cell-based therapies from early evaluation through to clinical and commercial supply.Business Wire BlogRoslinCT and BlueRock Therapeutics Partner to Expand Access to Clinical-Grade Pluripotent Cell Lines for Cell Therapy DevelopersRoslinCT and BlueRock Therapeutics have formed a strategic partnership to expand access to clinical-grade pluripotent stem cell lines for cell therapy developers. Under the agreement, RoslinCT will enable access to BlueRock's induced pluripotent stem cell lines alongside its own offerings, completing a technical transfer to its facilities in Scotland and Massachusetts. The partnership supports developers with services including cell banking, process development, and clinical and commercial manufacturing as pluripotent cell-based therapies advance through the clinic.FinancialContent Business PageRoslinCT and BlueRock Therapeutics Partner to Expand Access to Clinical-Grade Pluripotent Cell Lines for Cell Therapy DevelopersRoslinCT, a cell therapy contract development and manufacturing organization, has announced a strategic partnership with BlueRock Therapeutics to broaden access to clinical-grade pluripotent stem cell lines for cell therapy developers. The agreement includes a technical transfer of BlueRock's cell lines to RoslinCT's facilities in Scotland and Massachusetts, enabling RoslinCT to offer services including cell banking, process development, and GMP manufacturing for clinical and commercial use. Both companies aim to provide developers with a more comprehensive pathway to advance pluripotent cell-based therapies from early-stage evaluation through to commercial supply.EIN PresswireWho Is Gaining Ground in the Aplastic Anemia Market and WhyNovartis AG led global aplastic anemia sales in 2024 with an 8% market share, while the market is fragmented with the top 10 players holding 13% of revenue. The market is projected to grow to $9.08 billion by 2030 at a 5.1% CAGR, with strategic partnerships and advanced therapies driving competition.RegmednetCell therapy weekly: in vivo CAR-T therapy moves forwardRoslinCT and BOOST Pharma entered a strategic manufacturing partnership to support Phase III development of BT-101, an allogeneic mesenchymal stem cell therapy for Osteogenesis Imperfecta, with BOOST transferring its manufacturing process to RoslinCT's Edinburgh facilities. Autolus Therapeutics announced plans to evaluate Cellares' Cell Shuttle platform for commercial manufacturing of AUCATZYL® (obe-cel) to prepare for expansion into new indications including autoimmune diseases. The FDA cleared Kelonia Therapeutics' IND application for KLN-1010, an in vivo CAR-T therapy for relapsed and refractory multiple myeloma, enabling expansion of the Phase I trial to multiple US sites.BioSpaceRoslinCT and Ayrmid Ltd. Announce Expansion of Strategic Partnership to Manufacture Omisirge® (omidubicel-onlv) for Second FDA-Approved Indication in Severe Aplastic Anemia (SAA)RoslinCT and Ayrmid Ltd. have expanded their strategic partnership to include a commercial supply agreement for the manufacturing of Omisirge® for its second FDA-approved indication, severe aplastic anemia. This expansion leverages RoslinCT's facility in Hopkinton, MA, to support production following positive clinical trial results that broadened the therapy's patient population.PharmiWeb.comFDA approves Omisirge(R) as First Approved Cell Therapy to Treat Severe Aplastic AnemiaAyrmid Ltd., the parent company of Gamida Cell Inc., announced FDA approval for Omisirge (omidubicel-onlv) as a cell therapy for Severe Aplastic Anemia, based on a clinical study demonstrating 86% neutrophil recovery and 92% disease-free survival. The approval expands the use of Omisirge beyond its initial 2023 hematological malignancy indication and offers a transplant option for SAA patients who lack matched related donors. Ayrmid has partnered with RoslinCT to establish additional manufacturing capacity for Omisirge at its facility in Hopkinton, MA, beginning in 2027.GlobeNewswireRoslinCT to manufacture first-ever US FDA approved CRISPR-based gene therapy CASGEVY™ (exagamglogene autotemcel)RoslinCT will manufacture CASGEVY, the first FDA-approved CRISPR-based gene therapy for sickle cell disease, approved on 8 December 2023. The FDA is reviewing the therapy for transfusion-dependent beta thalassemia with a deadline of 20 March 2024.