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Aldevron

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uuid0004tol

Namestring
Aldevron
Legal namestring
Aldevron, LLC
Websiteurl
aldevron.com
Company typeenum
Private
Founded yearint
1998
Descriptiontext

Aldevron, founded in 1998 and headquartered in Fargo, North Dakota, is a global Contract Development and Manufacturing Organization (CDMO) specializing in biologics for genomic medicine. It is a wholly-owned subsidiary of Danaher Corporation (NYSE: DHR) and operates what the company describes as the world's largest cGMP plasmid DNA manufacturing facility (265,000 sq ft Breakthrough Campus with 32 production suites), supplemented by sites in Madison, WI (ISO 13485-certified protein manufacturing), Lincoln, NE, and a late-2025 Discovery Center in Waltham, MA. The company serves 1,000+ therapeutic companies across 1,100+ clinical trials and has produced 165,000+ lots since founding.

Its core platform spans custom and catalog products across four primary modalities: (1) plasmid DNA (traditional plasmids and the proprietary Nanoplasmid™ vector system with <500 bp backbone and RNA-OUT antibiotic-free selection); (2) mRNA drug substance and drug product, including LNP encapsulation via Precision Nanosystems, Cytiva, and Acuitas partnerships and sterile fill/finish via Cytiva SA25; (3) recombinant proteins and enzymes (including CRISPR nucleases such as SpyFi Cas9, Eureca-V, and SpCas9); and (4) CRISPR RNP manufacturing and cGMP gRNA (via IDT partnership). Process technologies include the HyperGRO™ fed-batch platform achieving yields up to 3.5 g/L and REVIVER™ engineered host strains for challenging plasmids, with a new Alchemy™ cell-free linear DNA offering launched in 2025.

Aldevron generates revenue through three streams: (1) contract development and manufacturing services (CDMO) with multi-year project-based contracts at research, GMP-Source™, small-scale cGMP (≤500 mg), and full cGMP quality grades; (2) catalog product sales via a direct e-commerce storefront for research-grade plasmids, CRISPR nucleases, viral vector plasmids, cloning backbones, IVT enzymes, and reporters ($150–$1,170+ list prices); and (3) managed storage and stability services (ASDS). The company sells direct to enterprise biopharma clients and distributes cGMP CRISPR nucleases globally through IDT. The go-to-market is primarily enterprise field sales for custom manufacturing, complemented by content marketing, webinars, and a flagship partnership channel with IDT. Regulatory track record includes FDA CBER Pre-License Inspection (NAI 2021), FDA Level 1 Surveillance Inspection (NAI 2024), EU GMP Compliance (June 2024), and ISO 13485:2016 renewal (July 2024).

Short descriptiontext

Aldevron is a global CDMO specializing in plasmid DNA, mRNA, recombinant proteins, and CRISPR components for genomic medicine developers, serving 1,000+ therapeutic companies across 1,100+ clinical trials. A wholly-owned Danaher subsidiary, it operates the world's largest cGMP plasmid DNA facility in Fargo, ND.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersFargo, United States
HQ citystring
Fargo
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices4 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
biologics contract manufacturing, plasmid DNA manufacturing, mRNA drug substance production, cell and gene therapy CDMO, CRISPR nucleases production
Industry3 codes
1Gene Therapy (Viral Vector/Plasmid) CDMO
CodeHLAGABAEPrimaryYes
2mRNA/LNP & Nucleic Acid Therapeutics CDMO
CodeHLAGABAFPrimaryNo
3Gene Therapy Vector Manufacturing & CDMO Services
CodeHLAAACAJPrimaryNo
NAICS code1 code
  • Pharmaceutical and Medicine Manufacturing3254
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Biologics Contract Development and Manufacturing (CDMO)
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model3 records
1Contract Development and Manufacturing Services
TypeProfessional Services
Description

Custom manufacturing services for plasmid DNA, mRNA, and proteins across research, GMP-Source, and cGMP quality grades. Revenue is generated through project-based contracts with biopharmaceutical companies for therapeutic development and manufacturing.

aldevron.com
2Catalog Product Sales
TypeOne Time License
Description

Standardized catalog products including CRISPR nucleases, viral vector plasmids, cloning backbones, IVT enzymes, and reporters sold through e-commerce platform. Products available at research grade, GMP-Source, and cGMP quality levels.

aldevron.com
3Storage and Stability Services
TypeManaged Services
Description

Aldevron Storage Distribution Services (ASDS) providing secure storage and stability testing for client materials including research-grade, GMP-Source, and GMP biological materials.

aldevron.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components6 values
Personnel, Infrastructure, Operations, Technology or R&D, Supply Chain, Marketing or Sales
Pricing details4 tiers
1cGMP Manufacturing Services for clinical and commercial applications
ModelOtherBilling cadenceMulti-year contract
Notes

Full cGMP manufacturing with highest quality oversight, process control, and segregated ISO-classified manufacturing suites. Pricing determined through project-specific quotes.

aldevron.com
2Small-Scale cGMP (≤500mg)
ModelOtherBilling cadenceMulti-year contract
Notes

Right-sized cGMP process for early-phase clinical trials using 10L working capacity fermenters. No engineering run required.

aldevron.com
3GMP-Source Grade
ModelUnit PricingBilling cadenceMulti-year contract
Notes

Cost-effective adoption of relevant cGMP manufacturing features for preclinical and early clinical applications.

aldevron.com
4Research Grade Products
ModelUnit PricingBilling cadencePay-as-you-go
Notes

Catalog products ranging from $150 (5mg plasmids) to $1,170+ (AAV helper plasmids 10mg). Volume discounts available.

store.aldevron.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 5 records shown
1Alchemy™
Description

Alchemy™ cell-free DNA technology - a cutting-edge service for manufacturing linear DNA.

aldevron.com
+4 more records
Core offering1 text field

Aldevron is a global Contract Development and Manufacturing Organization (CDMO) that produces plasmid DNA, mRNA, recombinant proteins, and CRISPR components for genomic medicine developers. The company offers custom manufacturing services across research, GMP-Source, and cGMP quality grades, along with standardized catalog products sold through an online storefront. Its offerings span gene therapy, cell therapy, gene editing, and mRNA vaccine/therapeutic applications, supporting clients from discovery through clinical and commercial stages.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • Delivered world's first mRNA-based personalized CRISPR therapy in 6 months - 3x faster than standard timelines
+4 more records
Product overview1 text field

Aldevron is a global Contract Development and Manufacturing Organization (CDMO) specializing in biologics manufacturing for genomic medicine. The company's product portfolio centers on a unified platform spanning plasmid DNA (traditional and Nanoplasmid™), mRNA (drug substance and drug product with LNP encapsulation), proteins, and CRISPR components. Aldevron offers products and services across the development continuum: catalog products for research use (CRISPR nucleases, IVT enzymes, viral vector plasmids, cloning backbones, reporters), custom manufacturing services at multiple quality grades (Research, GMP-Source™, Small-Scale cGMP, Traditional cGMP), and end-to-end solutions including cGMP gRNA, CRISPR RNP complex manufacturing, and storage/distribution services. The company's facilities include Breakthrough Campus (cGMP plasmid, mRNA, protein), Advance Campus (research-grade manufacturing), Innovate Campus Madison (protein manufacturing, ISO 13485), and the Discovery Center Waltham (cell-free DNA, gene editing, mRNA analytics). Quality offerings progress from research grade through cGMP to support clients from discovery through clinical to commercialization.

Product and service12 records
1Plasmid DNA Manufacturing
CategoryCustom Biologics Manufacturing
Description

Custom manufacturing of plasmid DNA for research, preclinical, clinical, and commercial applications. Available in research grade, GMP-Source (cost-effective cGMP manufacturing features), small-scale cGMP (≤500mg for early-phase trials), and traditional cGMP grades (>500mg to commercial scale). Supports traditional plasmids and Nanoplasmid vectors.

2Nanoplasmid DNA
CategoryCustom Biologics Manufacturing
Description

Next-generation plasmid vector system with <500 bp backbone and antibiotic-free selection (RNA-OUT). Offers high transgene expression, increased edited cell yields, improved safety profile, and enhanced manufacturing yields compared to traditional plasmids. Suitable for AAV, lentivirus, non-viral gene therapy, DNA vaccines, CRISPR gene editing, transposons, and mRNA vector protection.

3mRNA Drug Substance and Drug Product Manufacturing
CategoryCustom Biologics Manufacturing
Description

Complete mRNA manufacturing from sequence through final drug product. Includes drug substance manufacturing (cGMP batches released), LNP encapsulation via Cytiva and Acuitas partnership, and sterile fill/finish using Cytiva SA25 Aseptic Filling Workcell. Full analytics including sequence confirmation, particle sizing, encapsulation efficiency, and potency assays.

4Custom Protein/Enzyme Manufacturing
CategoryCustom Biologics Manufacturing
Description

Custom recombinant protein manufacturing from construct design through analytical testing. Services include host cell optimization, expression screening, process development, and contract production. Available for research, molecular diagnostic, and cGMP therapeutic applications. Madison, WI facility is ISO 13485 certified.

5CRISPR Ribonucleoprotein (RNP) Manufacturing
CategoryCustom Biologics Manufacturing
Description

Full RNP service solution combining Aldevron cGMP-grade CRISPR/Cas proteins with client-provided guide RNAs. Includes optimal complexing conditions, comprehensive characterization (free Cas9, free gRNA, RNP activity assays), and complete regulatory documentation for IND filing. Supports ex vivo and in vivo gene editing programs from discovery to clinic.

6cGMP gRNA Manufacturing and Sequencing
CategoryCustom Biologics Manufacturing
Description

cGMP guide RNA manufacturing services with robust analytical controls for preclinical and clinical trials. Partnership with IDT for oligonucleotide synthesis expertise. Includes engineering run and cGMP service levels with ISO 8 cleanroom certification, plus gRNA sequencing services for sequence-level identity verification and contaminant detection.

7CRISPR Nucleases (SpyFi Cas9, Eureca-V, SpCas9)
CategoryCatalog Products
Description

High-fidelity and wild-type CRISPR nucleases available in-stock at research grade and cGMP. SpyFi Cas9 Nuclease offers greater editing efficiency and reduced off-target effects. Eureca-V Nuclease is a Class 2 Type V nuclease based on MAD7 protein. SpCas9 Nuclease is wild-type for standard applications. All cGMP products include Drug Master File (DMF) on file with FDA.

8In vitro Transcription (IVT) & Capping Enzymes
CategoryCatalog Products
Description

Enzymes manufactured to support RNA synthesis from research through clinical trials and commercialization. Includes Codex HiCap RNA Polymerase for advancing RNA medicine. Supports mRNA vaccine and therapeutic development workflows.

9Viral Vector Plasmids (AAV & Lentiviral)
CategoryCatalog Products
Description

Viral expression and helper plasmids that generate high-titer viral vectors for research and clinical production. Includes AAV serotype-specific plasmids (AAV2, AAV5, AAV6) and lentiviral packaging plasmids. License and royalty free options available.

10REVIVER Host Strains and HyperGRO Manufacturing Platform
CategoryProprietary Manufacturing Technology
Description

Engineered E. coli host strains for stable high-yield production of polyA, ITR, and large palindrome-containing traditional plasmids. HyperGRO is an advanced fed-batch nutrient-limited process achieving yields up to 3.5 g/L. Both technologies optimize plasmid manufacturing performance and reduce costs.

11Aldevron Storage Distribution Services (ASDS)
CategoryStorage and Distribution Services
Description

Secure, monitored storage facility for research-grade, GMP-Source, and GMP biological materials. Temperature options from -80°C to ambient. Includes stability testing services with full QC assay panel tailored to client timelines and budgets.

12Alchemy Cell-free DNA Technology
CategoryCustom Biologics Manufacturing
Description

Cutting-edge cell-free linear DNA technology service launched to address advanced gene therapy and DNA vaccine manufacturing needs.

Scale indicator10 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-05-12
Description

Renewed lentiviral plasmid licensing agreement combining Aldevron's cGMP manufacturing expertise with Oxgene's advanced plasmid engineering capabilities to provide scalable plasmid solutions for cell and gene therapy developers. Partnership designed to help developers simplify supply chains, reduce manufacturing risk, and accelerate development timelines from discovery through clinical application.

Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2026-03-23
Description

Collaboration with San Raffaele Telethon Institute for Gene Therapy (SR-TIGET) - the first Danaher Beacon in the European Union - to advance next-generation genomic medicine platforms. Initiative combines SR-TIGET's scientific expertise with Cytiva's manufacturing capabilities and Aldevron's plasmid expertise, focusing on lentiviral vector production and homology-directed repair-based gene editing in hematopoietic stem cells.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2023-09-14
Description

Global distribution agreement where IDT stocks and sells Aldevron cGMP-manufactured CRISPR nucleases including SpyFi Cas9, Eureca-V, and SpCas9 nucleases to provide researchers with accelerated path to clinic. Combines IDT's expertise in CRISPR chemistry and oligo production with Aldevron's expertise in cGMP CRISPR nuclease and RNP manufacturing. Also includes collaboration on cGMP gRNA manufacturing as part of Danaher family.

Strategic tierStrategicTypeStrategic or Co-development PartnerAnnounced on2022-07-01
Description

Collaboration with Dr. Jennifer Doudna's IGI team for custom ultra-low endotoxin nuclease manufacturing to support injection-based delivery of CRISPR-Cas9 RNPs for central nervous system disorders research. Aldevron manufactured a custom nuclease meeting demanding specifications for the research program.

Strategic tierCoreTypeTechnology or Integration
Description

Partnership for LNP encapsulation technology to provide critical components for mRNA therapies. Aldevron collaborates with Precision Nanosystems to add scalability of LNP encapsulation from research grade to GMP for mRNA drug product manufacturing.

Strategic tierCoreTypeTechnology or Integration
Description

Collaboration for LNP delivery technology to support mRNA therapeutic development. Acuitas provides lipid nanoparticle technology for encapsulation of mRNA therapeutics manufactured at Aldevron facilities.

Strategic tierFlagshipTypeStrategic or Co-development Partner
Description

Partnership with CHOP to manufacture the world's first mRNA-based personalized CRISPR therapy for an infant with urea cycle disorder. Aldevron and IDT delivered the therapy in just six months - three times faster than standard timelines, demonstrating the power of integrated manufacturing and collaboration.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global large-molecule and cell-and-gene-therapy CDMO with substantially broader scale and modality coverage than Aldevron. Overlaps in plasmid, viral vector, mRNA, and cell therapy manufacturing, serving similar biopharma customers but as part of a much wider portfolio.

TypeDirect peer
Description

Houston-based CDMO specializing in plasmid DNA manufacturing for gene therapy, cell therapy, and DNA vaccine applications. Competes head-to-head with Aldevron in research-, GMP-Source-, and cGMP-grade plasmid services, including high-quality DNA vaccine and viral vector plasmids.

TypeBroad incumbent
Description

Large diversified CDMO (now under Novo Holdings) with established capabilities in biologics fill/finish, cell therapy, and plasmid/viral services. Overlaps with Aldevron in mRNA drug product, plasmid, and gene therapy manufacturing serving biopharma customers.

TypeBroad incumbent
Description

Global CDMO offering mammalian, microbial, and cell/gene therapy services including plasmid DNA and viral vector manufacturing. Overlaps with Aldevron in serving advanced therapy developers with cGMP-grade biologics manufacturing.

TypeDirect peer
Description

Specialist plasmid DNA and viral vector CDMO acquired by Charles River Laboratories. Directly competes with Aldevron in cGMP plasmid manufacturing for gene therapy and gene-modified cell therapy developers, with overlapping customer profiles in European and global advanced therapy biotechs.

TypeDirect peer
Description

U.S.-based viral vector and gene therapy CDMO offering lentiviral and AAV production. Competes with Aldevron for gene therapy developers needing integrated plasmid supply and viral vector manufacturing, with overlapping capabilities in early- to mid-stage clinical supply.

TypeBroad incumbent
Description

Major CRO/CDMO with a dedicated Cell and Gene Therapy CDMO segment (including Cobra Biologics and Vigene). Competes with Aldevron across plasmid DNA, viral vector, and cell therapy manufacturing for similar biopharmaceutical customers.

TypeBroad incumbent
Description

Large-scale biologics CDMO expanding into cell and gene therapy services. While primarily focused on mammalian biologics, its investments in mRNA and viral vector capabilities position it as an emerging overlapping competitor to Aldevron's CDMO services.

TypeEmerging player
Description

Technology-focused biomanufacturing company offering end-to-end production services across biologics, viral vectors, and nucleic acids. Competes with Aldevron in plasmid and viral vector manufacturing for advanced therapy developers, with a particular emphasis on integrated manufacturing platforms.

TypeRegional player
Description

France-based cell and gene therapy CDMO specializing in AAV and lentiviral vector manufacturing for European clients. Comparable to Aldevron in viral vector CDMO services and overlapping gene therapy customer base, though primarily serving EU-based developers.

Market position
Strengths5 records

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Headline, Details, Source

Weaknesses5 records

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Headline, Details, Source

Competitive moat6 records

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Type, Details

Key risks6 records

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Headline, Details, Source

Key highlights7 records

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Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

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

Segment5 records

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

Ideal customer profile5 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

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Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles15 records

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No data
Compliance5 records

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Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

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

Investors2 records

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

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

M&A

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 →

Aldevron

Biologics Contract Development and Manufacturing (CDMO)aldevron.com

Aldevron is a global CDMO specializing in plasmid DNA, mRNA, recombinant proteins, and CRISPR components for genomic medicine developers, serving 1,000+ therapeutic companies across 1,100+ clinical trials. A wholly-owned Danaher subsidiary, it operates the world's largest cGMP plasmid DNA facility in Fargo, ND.

What Aldevron does

Aldevron, founded in 1998 and headquartered in Fargo, North Dakota, is a global Contract Development and Manufacturing Organization (CDMO) specializing in biologics for genomic medicine. It is a wholly-owned subsidiary of Danaher Corporation (NYSE: DHR) and operates what the company describes as the world's largest cGMP plasmid DNA manufacturing facility (265,000 sq ft Breakthrough Campus with 32 production suites), supplemented by sites in Madison, WI (ISO 13485-certified protein manufacturing), Lincoln, NE, and a late-2025 Discovery Center in Waltham, MA. The company serves 1,000+ therapeutic companies across 1,100+ clinical trials and has produced 165,000+ lots since founding.

Its core platform spans custom and catalog products across four primary modalities: (1) plasmid DNA (traditional plasmids and the proprietary Nanoplasmid™ vector system with <500 bp backbone and RNA-OUT antibiotic-free selection); (2) mRNA drug substance and drug product, including LNP encapsulation via Precision Nanosystems, Cytiva, and Acuitas partnerships and sterile fill/finish via Cytiva SA25; (3) recombinant proteins and enzymes (including CRISPR nucleases such as SpyFi Cas9, Eureca-V, and SpCas9); and (4) CRISPR RNP manufacturing and cGMP gRNA (via IDT partnership). Process technologies include the HyperGRO™ fed-batch platform achieving yields up to 3.5 g/L and REVIVER™ engineered host strains for challenging plasmids, with a new Alchemy™ cell-free linear DNA offering launched in 2025.

Aldevron generates revenue through three streams: (1) contract development and manufacturing services (CDMO) with multi-year project-based contracts at research, GMP-Source™, small-scale cGMP (≤500 mg), and full cGMP quality grades; (2) catalog product sales via a direct e-commerce storefront for research-grade plasmids, CRISPR nucleases, viral vector plasmids, cloning backbones, IVT enzymes, and reporters ($150–$1,170+ list prices); and (3) managed storage and stability services (ASDS). The company sells direct to enterprise biopharma clients and distributes cGMP CRISPR nucleases globally through IDT. The go-to-market is primarily enterprise field sales for custom manufacturing, complemented by content marketing, webinars, and a flagship partnership channel with IDT. Regulatory track record includes FDA CBER Pre-License Inspection (NAI 2021), FDA Level 1 Surveillance Inspection (NAI 2024), EU GMP Compliance (June 2024), and ISO 13485:2016 renewal (July 2024).

Aldevron firmographics

Firmographics
Name
Aldevron
Legal name
Aldevron, LLC
Website
https://aldevron.com
Company type
Private
Founded year
1998
Operating status
Operating
Headcount range
101–250 employees
Short description
Aldevron is a global CDMO specializing in plasmid DNA, mRNA, recombinant proteins, and CRISPR components for genomic medicine developers, serving 1,000+ therapeutic companies across 1,100+ clinical trials. A wholly-owned Danaher subsidiary, it operates the world's largest cGMP plasmid DNA facility in Fargo, ND.
Ownership category
akta.pro rank

Aldevron industry classification

Industry
Product category
Biologics Contract Development and Manufacturing (CDMO)
NAICS
Pharmaceutical and Medicine Manufacturing (3254)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Gene Therapy (Viral Vector/Plasmid) CDMO (HLAGABAE)
akta.pro secondary industries
mRNA/LNP & Nucleic Acid Therapeutics CDMO (HLAGABAF), Gene Therapy Vector Manufacturing & CDMO Services (HLAAACAJ)

Keywords

  • Biologics contract manufacturing
  • Plasmid DNA manufacturing
  • MRNA drug substance production
  • Cell and gene therapy CDMO
  • CRISPR nucleases production

Where Aldevron is headquartered

Location

Headquarters

HQ city
Fargo
HQ country
United States
HQ region
North America

Offices4 records

Markets served

Aldevron business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Infrastructure, Operations, Technology or R&D, Supply Chain, Marketing or Sales

Revenue model

  1. Contract Development and Manufacturing Services: Custom manufacturing services for plasmid DNA, mRNA, and proteins across research, GMP-Source, and cGMP quality grades. Revenue is generated through project-based contracts with biopharmaceutical companies for therapeutic development and manufacturing.
  2. Catalog Product Sales: Standardized catalog products including CRISPR nucleases, viral vector plasmids, cloning backbones, IVT enzymes, and reporters sold through e-commerce platform. Products available at research grade, GMP-Source, and cGMP quality levels.
  3. Storage and Stability Services: Aldevron Storage Distribution Services (ASDS) providing secure storage and stability testing for client materials including research-grade, GMP-Source, and GMP biological materials.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractcGMP Manufacturing Services for clinical and commercial applications
OtherMulti-year contractSmall-Scale cGMP (≤500mg)
Unit PricingMulti-year contractGMP-Source Grade
Unit PricingPay-as-you-goResearch Grade Products

Go-to-market motion1 record

Distribution channels3 records

Marketing channels6 records

Aldevron product offering

Product offering

Core offering

Aldevron is a global Contract Development and Manufacturing Organization (CDMO) that produces plasmid DNA, mRNA, recombinant proteins, and CRISPR components for genomic medicine developers. The company offers custom manufacturing services across research, GMP-Source, and cGMP quality grades, along with standardized catalog products sold through an online storefront. Its offerings span gene therapy, cell therapy, gene editing, and mRNA vaccine/therapeutic applications, supporting clients from discovery through clinical and commercial stages.

Product overview

Aldevron is a global Contract Development and Manufacturing Organization (CDMO) specializing in biologics manufacturing for genomic medicine. The company's product portfolio centers on a unified platform spanning plasmid DNA (traditional and Nanoplasmid™), mRNA (drug substance and drug product with LNP encapsulation), proteins, and CRISPR components. Aldevron offers products and services across the development continuum: catalog products for research use (CRISPR nucleases, IVT enzymes, viral vector plasmids, cloning backbones, reporters), custom manufacturing services at multiple quality grades (Research, GMP-Source™, Small-Scale cGMP, Traditional cGMP), and end-to-end solutions including cGMP gRNA, CRISPR RNP complex manufacturing, and storage/distribution services. The company's facilities include Breakthrough Campus (cGMP plasmid, mRNA, protein), Advance Campus (research-grade manufacturing), Innovate Campus Madison (protein manufacturing, ISO 13485), and the Discovery Center Waltham (cell-free DNA, gene editing, mRNA analytics). Quality offerings progress from research grade through cGMP to support clients from discovery through clinical to commercialization.

Differentiator

Problem solved

Functional benefit

Brands

  • Alchemy™: Alchemy™ cell-free DNA technology - a cutting-edge service for manufacturing linear DNA.
  • REVIVER™
  • HyperGRO™
  • GMP-Source™
  • Nanoplasmid™

Products and services

  • Plasmid DNA Manufacturing Custom manufacturing of plasmid DNA for research, preclinical, clinical, and commercial applications. Available in research grade, GMP-Source (cost-effective cGMP manufacturing features), small-scale cGMP (≤500mg for early-phase trials), and traditional cGMP grades (>500mg to commercial scale). Supports traditional plasmids and Nanoplasmid vectors.
  • Nanoplasmid DNA Next-generation plasmid vector system with <500 bp backbone and antibiotic-free selection (RNA-OUT). Offers high transgene expression, increased edited cell yields, improved safety profile, and enhanced manufacturing yields compared to traditional plasmids. Suitable for AAV, lentivirus, non-viral gene therapy, DNA vaccines, CRISPR gene editing, transposons, and mRNA vector protection.
  • mRNA Drug Substance and Drug Product Manufacturing Complete mRNA manufacturing from sequence through final drug product. Includes drug substance manufacturing (cGMP batches released), LNP encapsulation via Cytiva and Acuitas partnership, and sterile fill/finish using Cytiva SA25 Aseptic Filling Workcell. Full analytics including sequence confirmation, particle sizing, encapsulation efficiency, and potency assays.
  • Custom Protein/Enzyme Manufacturing Custom recombinant protein manufacturing from construct design through analytical testing. Services include host cell optimization, expression screening, process development, and contract production. Available for research, molecular diagnostic, and cGMP therapeutic applications. Madison, WI facility is ISO 13485 certified.
  • CRISPR Ribonucleoprotein (RNP) Manufacturing Full RNP service solution combining Aldevron cGMP-grade CRISPR/Cas proteins with client-provided guide RNAs. Includes optimal complexing conditions, comprehensive characterization (free Cas9, free gRNA, RNP activity assays), and complete regulatory documentation for IND filing. Supports ex vivo and in vivo gene editing programs from discovery to clinic.
  • cGMP gRNA Manufacturing and Sequencing cGMP guide RNA manufacturing services with robust analytical controls for preclinical and clinical trials. Partnership with IDT for oligonucleotide synthesis expertise. Includes engineering run and cGMP service levels with ISO 8 cleanroom certification, plus gRNA sequencing services for sequence-level identity verification and contaminant detection.
  • CRISPR Nucleases (SpyFi Cas9, Eureca-V, SpCas9) High-fidelity and wild-type CRISPR nucleases available in-stock at research grade and cGMP. SpyFi Cas9 Nuclease offers greater editing efficiency and reduced off-target effects. Eureca-V Nuclease is a Class 2 Type V nuclease based on MAD7 protein. SpCas9 Nuclease is wild-type for standard applications. All cGMP products include Drug Master File (DMF) on file with FDA.
  • In vitro Transcription (IVT) & Capping Enzymes Enzymes manufactured to support RNA synthesis from research through clinical trials and commercialization. Includes Codex HiCap RNA Polymerase for advancing RNA medicine. Supports mRNA vaccine and therapeutic development workflows.
  • Viral Vector Plasmids (AAV & Lentiviral) Viral expression and helper plasmids that generate high-titer viral vectors for research and clinical production. Includes AAV serotype-specific plasmids (AAV2, AAV5, AAV6) and lentiviral packaging plasmids. License and royalty free options available.
  • REVIVER Host Strains and HyperGRO Manufacturing Platform Engineered E. coli host strains for stable high-yield production of polyA, ITR, and large palindrome-containing traditional plasmids. HyperGRO is an advanced fed-batch nutrient-limited process achieving yields up to 3.5 g/L. Both technologies optimize plasmid manufacturing performance and reduce costs.
  • Aldevron Storage Distribution Services (ASDS) Secure, monitored storage facility for research-grade, GMP-Source, and GMP biological materials. Temperature options from -80°C to ambient. Includes stability testing services with full QC assay panel tailored to client timelines and budgets.
  • Alchemy Cell-free DNA Technology Cutting-edge cell-free linear DNA technology service launched to address advanced gene therapy and DNA vaccine manufacturing needs.

Quantifiable outcome

  • Delivered world's first mRNA-based personalized CRISPR therapy in 6 months - 3x faster than standard timelines
  • +4 more outcomes

Companies that use Aldevron

Customer profile

Named customers3 records

Segments5 records

Ideal customer profiles5 records

Aldevron technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature7 records

Aldevron partnerships and signals

Strategic signal

Partnerships

Seven partnerships are on record, tiered core, flagship and strategic.

  • MinariscoreStrategic or Co-development Partner · 12 May 2026Renewed lentiviral plasmid licensing agreement combining Aldevron's cGMP manufacturing expertise with Oxgene's advanced plasmid engineering capabilities to provide scalable plasmid solutions for cell and gene therapy developers. Partnership designed to help developers simplify supply chains, reduce manufacturing risk, and accelerate development timelines from discovery through clinical application.
  • CytivaflagshipStrategic or Co-development Partner · 23 March 2026Collaboration with San Raffaele Telethon Institute for Gene Therapy (SR-TIGET) - the first Danaher Beacon in the European Union - to advance next-generation genomic medicine platforms. Initiative combines SR-TIGET's scientific expertise with Cytiva's manufacturing capabilities and Aldevron's plasmid expertise, focusing on lentiviral vector production and homology-directed repair-based gene editing in hematopoietic stem cells.
  • Integrated DNA Technologies (IDT)coreChannel Partner/ Reseller/ Distributor · 14 September 2023Global distribution agreement where IDT stocks and sells Aldevron cGMP-manufactured CRISPR nucleases including SpyFi Cas9, Eureca-V, and SpCas9 nucleases to provide researchers with accelerated path to clinic. Combines IDT's expertise in CRISPR chemistry and oligo production with Aldevron's expertise in cGMP CRISPR nuclease and RNP manufacturing. Also includes collaboration on cGMP gRNA manufacturing as part of Danaher family.
  • Innovative Genomics Institute (IGI)strategicStrategic or Co-development Partner · 1 July 2022Collaboration with Dr. Jennifer Doudna's IGI team for custom ultra-low endotoxin nuclease manufacturing to support injection-based delivery of CRISPR-Cas9 RNPs for central nervous system disorders research. Aldevron manufactured a custom nuclease meeting demanding specifications for the research program.
  • Precision NanosystemscoreTechnology or IntegrationPartnership for LNP encapsulation technology to provide critical components for mRNA therapies. Aldevron collaborates with Precision Nanosystems to add scalability of LNP encapsulation from research grade to GMP for mRNA drug product manufacturing.
  • Acuitas TherapeuticscoreTechnology or IntegrationCollaboration for LNP delivery technology to support mRNA therapeutic development. Acuitas provides lipid nanoparticle technology for encapsulation of mRNA therapeutics manufactured at Aldevron facilities.
  • Children's Hospital of Philadelphia (CHOP)flagshipStrategic or Co-development PartnerPartnership with CHOP to manufacture the world's first mRNA-based personalized CRISPR therapy for an infant with urea cycle disorder. Aldevron and IDT delivered the therapy in just six months - three times faster than standard timelines, demonstrating the power of integrated manufacturing and collaboration.

Scale indicators10 records

Recent moves7 records

Expansion highlights6 records

Aldevron competitors and assessment

Company assessment

Broad incumbents

  • Lonza: Global large-molecule and cell-and-gene-therapy CDMO with substantially broader scale and modality coverage than Aldevron. Overlaps in plasmid, viral vector, mRNA, and cell therapy manufacturing, serving similar biopharma customers but as part of a much wider portfolio.
  • Catalent: Large diversified CDMO (now under Novo Holdings) with established capabilities in biologics fill/finish, cell therapy, and plasmid/viral services. Overlaps with Aldevron in mRNA drug product, plasmid, and gene therapy manufacturing serving biopharma customers.
  • AGC Biologics: Global CDMO offering mammalian, microbial, and cell/gene therapy services including plasmid DNA and viral vector manufacturing. Overlaps with Aldevron in serving advanced therapy developers with cGMP-grade biologics manufacturing.
  • Charles River Laboratories: Major CRO/CDMO with a dedicated Cell and Gene Therapy CDMO segment (including Cobra Biologics and Vigene). Competes with Aldevron across plasmid DNA, viral vector, and cell therapy manufacturing for similar biopharmaceutical customers.
  • Samsung Biologics: Large-scale biologics CDMO expanding into cell and gene therapy services. While primarily focused on mammalian biologics, its investments in mRNA and viral vector capabilities position it as an emerging overlapping competitor to Aldevron's CDMO services.

Direct peers

  • VGXI: Houston-based CDMO specializing in plasmid DNA manufacturing for gene therapy, cell therapy, and DNA vaccine applications. Competes head-to-head with Aldevron in research-, GMP-Source-, and cGMP-grade plasmid services, including high-quality DNA vaccine and viral vector plasmids.
  • Cobra Biologics (Charles River): Specialist plasmid DNA and viral vector CDMO acquired by Charles River Laboratories. Directly competes with Aldevron in cGMP plasmid manufacturing for gene therapy and gene-modified cell therapy developers, with overlapping customer profiles in European and global advanced therapy biotechs.
  • Genezen: U.S.-based viral vector and gene therapy CDMO offering lentiviral and AAV production. Competes with Aldevron for gene therapy developers needing integrated plasmid supply and viral vector manufacturing, with overlapping capabilities in early- to mid-stage clinical supply.

Emerging players

  • National Resilience: Technology-focused biomanufacturing company offering end-to-end production services across biologics, viral vectors, and nucleic acids. Competes with Aldevron in plasmid and viral vector manufacturing for advanced therapy developers, with a particular emphasis on integrated manufacturing platforms.

Regional players

  • Yposkesi: France-based cell and gene therapy CDMO specializing in AAV and lentiviral vector manufacturing for European clients. Comparable to Aldevron in viral vector CDMO services and overlapping gene therapy customer base, though primarily serving EU-based developers.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Aldevron social profiles

Digital presence

Aldevron compliance and trust

Trust signal

Compliance5 records

Aldevron financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Aldevron leadership team

Management profile

Number of profiles

Profiles15 records

Aldevron funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors2 records

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

Aldevron M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about Aldevron

What does Aldevron do?

Aldevron is a global Contract Development and Manufacturing Organization (CDMO) that produces plasmid DNA, mRNA, recombinant proteins, and CRISPR components for genomic medicine developers. The company offers custom manufacturing services across research, GMP-Source, and cGMP quality grades, along with standardized catalog products sold through an online storefront. Its offerings span gene therapy, cell therapy, gene editing, and mRNA vaccine/therapeutic applications, supporting clients from discovery through clinical and commercial stages.

Is Aldevron a public or private company?

Aldevron is a private company. It is classified as corporate owned and is currently operating.

When was Aldevron founded?

Aldevron was founded in 1998. It employs 101 to 250 people.

Where is Aldevron based?

Aldevron is headquartered in Fargo, United States, in the North America region.

How does Aldevron make money?

Three revenue lines are on record. Contract Development and Manufacturing Services are the primary driver. The others are catalog Product Sales and storage and Stability Services.

Who are Aldevron's main competitors?

Broad incumbents on record are Lonza, Catalent, AGC Biologics, Charles River Laboratories and Samsung Biologics. Direct peers are VGXI, Cobra Biologics (Charles River) and Genezen. National Resilience is listed as an emerging player. Yposkesi is listed as a regional player.

Does Aldevron have an API?

No public API is recorded for Aldevron.

What industry is Aldevron in?

Aldevron's product category is Biologics Contract Development and Manufacturing (CDMO). Its primary akta.pro industry code is HLAGABAE, Gene Therapy (Viral Vector/Plasmid) CDMO, with a secondary code of HLAGABAF, mRNA/LNP & Nucleic Acid Therapeutics CDMO. Its NAICS code is 3254 and its SIC code is 2834.

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Live signals
News-MedicalIntegrated DNA Technologies and Aldevron launch new Cas9 mRNA solutions to accelerate path from gene editing research to developmentIntegrated DNA Technologies and Aldevron launched research-grade S.p. Cas9 mRNA in wild type and SpyFi high-fidelity formats. The mRNA is enzymatically capped and compatible with electroporation, cationic lipids, and lipid nanoparticles, with a path to CGMP-manufactured versions. Base and prime editors are planned later this year.FinancialContent Business PageIntegrated DNA Technologies and Aldevron Launch New Cas9 mRNA Solutions to Accelerate Path from Gene Editing Research to DevelopmentIntegrated DNA Technologies and Aldevron launched research-grade S.p. Cas9 mRNA in wild type and SpyFi high-fidelity formats. The co-developed offering combines IDT's CRISPR expertise with Aldevron's mRNA manufacturing, targeting high on-target editing and reduced off-target activity. It is the first in a suite of co-developed offerings, with base and prime editors planned later this year.Stock TitanDanaher Companies Launch Cas9 mRNA Gene-Editing ToolIntegrated DNA Technologies and Aldevron launched co-developed Cas9 mRNA tools in research-grade wild type and SpyFi high-fidelity formats. The offering combines IDT's CRISPR engineering with Aldevron's mRNA manufacturing to support CRISPR-based research, with a path to CGMP-manufactured versions. Base and prime editors are planned later this year.Business Wire BlogIntegrated DNA Technologies and Aldevron Launch New Cas9 mRNA Solutions to Accelerate Path from Gene Editing Research to DevelopmentIntegrated DNA Technologies and Aldevron launched research-grade Cas9 mRNA in wild type and SpyFi high-fidelity formats. The offering supports CRISPR editing across cell types and delivery methods, with a path to CGMP-manufactured versions. Base and prime editors are planned later this year.MDPIBackbone-Minimised Nanoplasmid DNA Systems Enable High-Titre AAV Production in Suspension HEK293 PlatformsResearchers at University College London and the UK Medicines and Healthcare Products Regulatory Agency evaluated compact Nanoplasmid™ DNA constructs (manufactured by Aldevron) as a replacement for conventional large backbone plasmids in adeno-associated virus (AAV) production using suspension HEK293 cells.BiobuzzAldevron and Minaris Renew Lentiviral Plasmid Agreement to Accelerate Cell and Gene Therapy DevelopmentAldevron and Minaris have renewed their lentiviral plasmid licensing agreement to provide scalable plasmid solutions for cell and gene therapy developers. Under the expanded agreement, Aldevron will continue manufacturing and supplying plasmid systems across multiple quality grades, combining its cGMP manufacturing expertise with Oxgene's advanced plasmid engineering capabilities. The partnership is designed to help developers simplify supply chains, reduce manufacturing risk, and accelerate development timelines from discovery through clinical application.BioSpaceAldevron and Minaris Renew Lentiviral Plasmid Agreement to Accelerate Gene-Modified Cell Therapy DevelopmentAldevron and Minaris renewed a licensing agreement to expand access to a proprietary lentiviral plasmid system for gene-modified cell therapy. The agreement offers off-the-shelf plasmids at research, GMP Source, and cGMP quality grades, aiming to reduce lead times and accelerate development. It builds on Aldevron's partnership with Oxgene, Minaris' viral vector platform.EIN PresswiremRNA Therapeutics CDMO Market Competition Trends and Industry PositioningLonza Group led global mRNA therapeutics CDMO sales in 2024 with a 5% market share, while the top 10 players held 36% of total revenue. Leading firms include Thermo Fisher, Samsung Biologics, and WuXi Biologics, with emerging CDMOs intensifying competition. Strategic collaborations and capacity expansions are expected to strengthen leading players.AldevronOvercoming Scalability Challenges in AAV ManufacturingThe article examines persistent scalability challenges in AAV vector manufacturing for gene therapy, noting that despite projected 18-22% CAGR growth in the global market, process variability and raw material constraints continue to impede clinical and commercial advancement. The Testa Center in Uppsala, Sweden—a public-private initiative between the Swedish government and Cytiva—operates a pilot-scale, non-GMP bioprocessing facility where researchers can test and validate AAV manufacturing innovations under industrial conditions before committing to full cGMP scale. For the Testa Challenge program, Aldevron is supplying production-grade plasmid DNA to ensure consistent, high-quality inputs that enable participating teams to accurately evaluate their process technologies without raw material inconsistencies interfering with results.DrugdiscoverynewsRare disease programs are pushing innovation faster than everIn 2025, Baby KJ Muldoon became the first patient to receive a personalized mRNA-based CRISPR gene editing therapy through collaboration between academic teams and industry manufacturers including Aldevron and Integrated DNA Technologies. On February 23, 2026, the FDA issued draft guidance for individualized gene editing and RNA-based therapies targeting ultra-rare diseases, establishing new regulatory pathways for treatments that cannot rely on traditional randomized controlled trials. The article argues that despite funding challenges in the biotechnology sector, rare disease programs continue to drive innovation by combining scientific breakthroughs with manufacturing and regulatory alignment.