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BioVectra

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uuid0000o41

Namestring
BioVectra
Legal namestring
BIOVECTRA Inc.
Websiteurl
biovectra.com
Company typeenum
Private
Founded yearint
1970
Descriptiontext

BioVectra is a full-service contract development and manufacturing organization (CDMO) headquartered in Charlottetown, Prince Edward Island, Canada, with operations dating to 1970. The company provides clinical-to-commercial scale manufacturing services to the global pharmaceutical and biotechnology industry, with an enterprise-focused customer base that includes 18 of the top 20 global pharma and biotech companies. BioVectra serves more than 100 active clients across multiple geographies, earning revenue primarily through fee-for-service contract manufacturing agreements that span process development, analytical method development, GMP manufacturing, and fill-finish operations.

BioVectra's technology platform integrates four core manufacturing modalities: microbial fermentation (supporting recombinant proteins, plasmid DNA, and antibody fragments using BSL-1 systems including E. coli and Pichia pastoris), mammalian cell culture, complex synthetic chemistry for small molecule APIs, and aseptic fill-finish with capacity for up to 40,000 filled vials per day. The company also operates specialized HPAPI manufacturing capabilities with OELs down to 20 ng/m³ (SafeBridge Band 3 & 4), and end-to-end mRNA and plasmid DNA production capabilities including LNP formulation, integrated through a 36,000 sq ft mRNA Biomanufacturing Centre. Five GMP-certified facilities across Atlantic Canada anchor these capabilities, supported by strategic partnerships with Revolution Biomanufacturing (mRNA design) and Acuitas Therapeutics (LNP delivery technology).

The business operates on a project-based revenue model with multi-year supply contracts, where pricing is negotiated per project based on molecule complexity, manufacturing scale, and regulatory pathway. Distribution is exclusively through direct enterprise sales with dedicated business development teams engaging top-tier pharma and biotech clients. Following its September 2024 acquisition by Agilent Technologies for $925 million, BioVectra now operates as part of Agilent's Diagnostics and Genomics Group and serves as the foundation of Agilent Advanced Therapeutics, a unified CDMO platform launched in March 2026 that integrates BioVectra's Canadian operations with Agilent's Nucleic Acid Solutions in Colorado.

Short descriptiontext

BioVectra is a Canadian full-service CDMO providing clinical-to-commercial scale contract manufacturing of biologics, small molecules, HPAPIs, mRNA/pDNA, and aseptic fill-finish products, serving 18 of the top 20 global pharmaceutical and biotechnology companies from five GMP facilities in Atlantic Canada, now operating within Agilent Advanced Therapeutics.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersCharlottetown, Canada
HQ citystring
Charlottetown
HQ countrystring
Canada
HQ regionstring
North America
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
contract manufacturing services, active pharmaceutical ingredients, biologics manufacturing, microbial fermentation services, aseptic fill-finish
Industry5 codes
1Biologics (mAbs/Recombinant Proteins) CDMO
CodeHLAGABACPrimaryYes
2mRNA & Nucleic Acid Manufacturing Services (mRNA/saRNA/Plasmid DNA)
CodeHLAGAGACPrimaryNo
3Sterile Fill-Finish & Aseptic Manufacturing CDMO
CodeHLAGABAHPrimaryNo
4Small-Molecule Drug Product (Solid/Oral/Parenteral) CDMO
CodeHLAGABABPrimaryNo
5Clinical Trial Material (CTM) Manufacturing & Supply CDMO
CodeHLAGABAKPrimaryNo
NAICS code4 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
  • Pharmaceutical and Medicine Manufacturing3254
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code3 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
  • Services-Commercial Physical & Biological Research8731
Product category
Pharmaceutical Contract Manufacturing
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Contract Manufacturing Services
TypeOne Time License
Description

BioVectra generates revenue primarily through fee-for-service contract manufacturing agreements. Customers engage BioVectra for specific stages of drug development and commercial production, including process development, analytical method development, GMP manufacturing, and fill-finish. Revenue is earned as services are rendered or upon milestone completion under long-term supply contracts. The model is project-based and recurring through multi-year client relationships.

Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components5 values
Personnel, Operations, Infrastructure, Technology or R&D, Supply Chain
Pricing details1 tier
1Custom project-based pricing
ModelOtherBilling cadenceMulti-year contract
Notes

As a CDMO providing bespoke manufacturing services, pricing is negotiated per project and reflects scope of work, molecule type, manufacturing scale, and regulatory pathway.

GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

BioVectra is a full-service Contract Development and Manufacturing Organization (CDMO) providing clinical-to-commercial scale production of biologics, synthetic small molecules, plasmid DNA/mRNA, lipid nanoparticles (LNP), highly potent APIs (HPAPIs), bioreagents, and aseptic fill-finished drug products. The company operates five GMP manufacturing facilities across Atlantic Canada, leveraging microbial fermentation, mammalian cell culture, synthetic chemistry, and sterile fill-finish capabilities to serve global pharmaceutical and biotechnology clients.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Serves 18 of the top 20 global pharmaceutical and biotechnology companies
+2 more records
Product overview1 text field

BIOVECTRA is a full-service CDMO (Contract Development and Manufacturing Organization) offering clinical-to-commercial scale production across multiple therapeutic modalities. The company operates as a unified platform with core capabilities including Biologics Manufacturing (microbial fermentation, recombinant proteins, pDNA, mRNA), Synthetic Small Molecules (complex chemistry, APIs), Highly Potent APIs (HPAPIs), Fermented Small Molecules, Bioreagents, Fill/Finish Services, and Gene Editing Manufacturing. Under the Agilent Advanced Therapeutics platform, BIOVECTRA provides end-to-end services from discovery through commercial manufacturing, supported by Project Support Services for process engineering, quality, and regulatory expertise. The company maintains 5 GMP facilities across Prince Edward Island and Nova Scotia, Canada, with specialized mRNA biomanufacturing capacity of 160 million doses per year.

Product and service1 record
1Biologics Manufacturing
Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-11-06
Description

Strategic partnership enabling integrated mRNA design and GMP production services. The collaboration combines BioVectra's CDMO capabilities with Revolution Biomanufacturing's mRNA platform expertise, providing clients a streamlined path from mRNA design through GMP manufacturing. Announced November 6, 2025.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Service agreement providing BioVectra clients access to Acuitas Therapeutics' industry-leading lipid nanoparticle (LNP) delivery system technology. This enables integrated mRNA development and delivery solutions for clients developing mRNA-based therapeutics and vaccines.

Strategic tierSupportingTypeStrategic or Co-development Partner
Description

BioVectra is part of a Canadian ecosystem of advanced therapy partners including CCRM (cell and gene therapy), Cytiva/Precision Nanosystems (nanotechnology delivery), Northern RNA (RNA manufacturing), and OmniaBio (biologics and cell therapy manufacturing). Together, these organizations offer an integrated Canadian supply chain solution for immunotherapies and lentiviral vector development, reducing the need for Canadian biotech companies to seek manufacturing capabilities outside the country.

Recent move10 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global CDMO leader offering microbial and mammalian biologics manufacturing, mRNA services, and fill-finish. Comparable as a full-service CDMO serving top-20 pharma with similar integrated modality breadth, though at significantly larger scale.

TypeBroad incumbent
Description

Major global CDMO with biologics, fill-finish, and nucleic acid manufacturing capabilities. Comparable in offering CDMO services across biologics modalities and serving large pharma; differs in its broader oral and softgel specialty franchise.

TypeDirect peer
Description

Mid-to-large CDMO specializing in microbial and mammalian biologics, gene therapy, and mRNA manufacturing. Directly comparable to BioVectra in microbial fermentation focus and CDMO service model for biologics and nucleic acids.

TypeDirect peer
Description

European-based CDMO offering biologics, fill-finish, and small molecule API manufacturing. Comparable as a full-service CDMO with similar project-based revenue model serving pharma clients, though with different geographic footprint.

TypeDirect peer
Description

CDMO specializing in microbial and mammalian cell culture-based biopharmaceuticals with aseptic fill-finish. Directly comparable to BioVectra's biologics core, with similar mid-tier scale and European-headquartered operations.

TypeBroad incumbent
Description

Large CDMO offering microbial and mammalian biologics, gene therapy, and vaccines manufacturing. Comparable in integrated biologics CDMO services with microbial fermentation expertise; larger scale and broader global footprint.

TypeBroad incumbent
Description

World's largest biologics CDMO with end-to-end microbial and mammalian services, including mRNA. Comparable CDMO offering across biologics modalities and top-20 pharma clients; significant pricing pressure on North American CDMOs.

TypeBroad incumbent
Description

Large-scale biologics CDMO with substantial mammalian cell culture capacity. Comparable in serving top-20 pharma with biologics manufacturing, but at much larger scale with different geographic footprint.

TypeDirect peer
Description

European CDMO offering biologics, small molecule API, and HPAPI manufacturing services. Comparable as a mid-tier integrated CDMO with similar modality breadth and project-based revenue model.

TypeDirect peer
Description

Swiss CDMO specializing in sterile injectable fill-finish and biologics manufacturing for challenging modalities. Comparable in aseptic fill-finish and biologics capabilities, particularly for small-to-mid-sized pharma clients seeking specialized services.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Customer concentration

Classification, Details

Named customers1 record

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 profile1 record

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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles12 records

Each record includes

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

No data
No data
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&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 →

BioVectra

Pharmaceutical Contract Manufacturingbiovectra.com

BioVectra is a Canadian full-service CDMO providing clinical-to-commercial scale contract manufacturing of biologics, small molecules, HPAPIs, mRNA/pDNA, and aseptic fill-finish products, serving 18 of the top 20 global pharmaceutical and biotechnology companies from five GMP facilities in Atlantic Canada, now operating within Agilent Advanced Therapeutics.

What BioVectra does

BioVectra is a full-service contract development and manufacturing organization (CDMO) headquartered in Charlottetown, Prince Edward Island, Canada, with operations dating to 1970. The company provides clinical-to-commercial scale manufacturing services to the global pharmaceutical and biotechnology industry, with an enterprise-focused customer base that includes 18 of the top 20 global pharma and biotech companies. BioVectra serves more than 100 active clients across multiple geographies, earning revenue primarily through fee-for-service contract manufacturing agreements that span process development, analytical method development, GMP manufacturing, and fill-finish operations.

BioVectra's technology platform integrates four core manufacturing modalities: microbial fermentation (supporting recombinant proteins, plasmid DNA, and antibody fragments using BSL-1 systems including E. coli and Pichia pastoris), mammalian cell culture, complex synthetic chemistry for small molecule APIs, and aseptic fill-finish with capacity for up to 40,000 filled vials per day. The company also operates specialized HPAPI manufacturing capabilities with OELs down to 20 ng/m³ (SafeBridge Band 3 & 4), and end-to-end mRNA and plasmid DNA production capabilities including LNP formulation, integrated through a 36,000 sq ft mRNA Biomanufacturing Centre. Five GMP-certified facilities across Atlantic Canada anchor these capabilities, supported by strategic partnerships with Revolution Biomanufacturing (mRNA design) and Acuitas Therapeutics (LNP delivery technology).

The business operates on a project-based revenue model with multi-year supply contracts, where pricing is negotiated per project based on molecule complexity, manufacturing scale, and regulatory pathway. Distribution is exclusively through direct enterprise sales with dedicated business development teams engaging top-tier pharma and biotech clients. Following its September 2024 acquisition by Agilent Technologies for $925 million, BioVectra now operates as part of Agilent's Diagnostics and Genomics Group and serves as the foundation of Agilent Advanced Therapeutics, a unified CDMO platform launched in March 2026 that integrates BioVectra's Canadian operations with Agilent's Nucleic Acid Solutions in Colorado.

BioVectra firmographics

Firmographics
Name
BioVectra
Legal name
BIOVECTRA Inc.
Website
https://biovectra.com
Company type
Private
Founded year
1970
Operating status
Operating
Headcount range
501–1,000 employees
Short description
BioVectra is a Canadian full-service CDMO providing clinical-to-commercial scale contract manufacturing of biologics, small molecules, HPAPIs, mRNA/pDNA, and aseptic fill-finish products, serving 18 of the top 20 global pharmaceutical and biotechnology companies from five GMP facilities in Atlantic Canada, now operating within Agilent Advanced Therapeutics.
Ownership category
akta.pro rank

BioVectra industry classification

Industry
Product category
Pharmaceutical Contract Manufacturing
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412), Pharmaceutical and Medicine Manufacturing (3254), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834), Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Biologics (mAbs/Recombinant Proteins) CDMO (HLAGABAC)
akta.pro secondary industries
mRNA & Nucleic Acid Manufacturing Services (mRNA/saRNA/Plasmid DNA) (HLAGAGAC), Sterile Fill-Finish & Aseptic Manufacturing CDMO (HLAGABAH), Small-Molecule Drug Product (Solid/Oral/Parenteral) CDMO (HLAGABAB), Clinical Trial Material (CTM) Manufacturing & Supply CDMO (HLAGABAK)

Keywords

  • Contract manufacturing services
  • Active pharmaceutical ingredients
  • Biologics manufacturing
  • Microbial fermentation services
  • Aseptic fill-finish

Where BioVectra is headquartered

Location

Headquarters

HQ city
Charlottetown
HQ country
Canada
HQ region
North America

Offices3 records

Markets served

BioVectra business model

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

Revenue model

  1. Contract Manufacturing Services: BioVectra generates revenue primarily through fee-for-service contract manufacturing agreements. Customers engage BioVectra for specific stages of drug development and commercial production, including process development, analytical method development, GMP manufacturing, and fill-finish. Revenue is earned as services are rendered or upon milestone completion under long-term supply contracts. The model is project-based and recurring through multi-year client relationships.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractCustom project-based pricing

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

BioVectra product offering

Product offering

Core offering

BioVectra is a full-service Contract Development and Manufacturing Organization (CDMO) providing clinical-to-commercial scale production of biologics, synthetic small molecules, plasmid DNA/mRNA, lipid nanoparticles (LNP), highly potent APIs (HPAPIs), bioreagents, and aseptic fill-finished drug products. The company operates five GMP manufacturing facilities across Atlantic Canada, leveraging microbial fermentation, mammalian cell culture, synthetic chemistry, and sterile fill-finish capabilities to serve global pharmaceutical and biotechnology clients.

Product overview

BIOVECTRA is a full-service CDMO (Contract Development and Manufacturing Organization) offering clinical-to-commercial scale production across multiple therapeutic modalities. The company operates as a unified platform with core capabilities including Biologics Manufacturing (microbial fermentation, recombinant proteins, pDNA, mRNA), Synthetic Small Molecules (complex chemistry, APIs), Highly Potent APIs (HPAPIs), Fermented Small Molecules, Bioreagents, Fill/Finish Services, and Gene Editing Manufacturing. Under the Agilent Advanced Therapeutics platform, BIOVECTRA provides end-to-end services from discovery through commercial manufacturing, supported by Project Support Services for process engineering, quality, and regulatory expertise. The company maintains 5 GMP facilities across Prince Edward Island and Nova Scotia, Canada, with specialized mRNA biomanufacturing capacity of 160 million doses per year.

Differentiator

Problem solved

Functional benefit

Products and services

  • Biologics Manufacturing

Quantifiable outcome

  • Serves 18 of the top 20 global pharmaceutical and biotechnology companies
  • +2 more outcomes

Companies that use BioVectra

Customer profile

Named customers1 record

Segments1 record

Ideal customer profiles1 record

BioVectra technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

BioVectra partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered core and supporting.

  • Revolution BiomanufacturingcoreStrategic or Co-development Partner · 6 November 2025Strategic partnership enabling integrated mRNA design and GMP production services. The collaboration combines BioVectra's CDMO capabilities with Revolution Biomanufacturing's mRNA platform expertise, providing clients a streamlined path from mRNA design through GMP manufacturing. Announced November 6, 2025.
  • Acuitas TherapeuticscoreStrategic or Co-development PartnerService agreement providing BioVectra clients access to Acuitas Therapeutics' industry-leading lipid nanoparticle (LNP) delivery system technology. This enables integrated mRNA development and delivery solutions for clients developing mRNA-based therapeutics and vaccines.
  • CCRM, Cytiva (Precision Nanosystems), Northern RNA, OmniaBiosupportingStrategic or Co-development PartnerBioVectra is part of a Canadian ecosystem of advanced therapy partners including CCRM (cell and gene therapy), Cytiva/Precision Nanosystems (nanotechnology delivery), Northern RNA (RNA manufacturing), and OmniaBio (biologics and cell therapy manufacturing). Together, these organizations offer an integrated Canadian supply chain solution for immunotherapies and lentiviral vector development, reducing the need for Canadian biotech companies to seek manufacturing capabilities outside the country.

Scale indicators6 records

Recent moves10 records

Expansion highlights6 records

BioVectra competitors and assessment

Company assessment

Broad incumbents

  • Lonza Group: Global CDMO leader offering microbial and mammalian biologics manufacturing, mRNA services, and fill-finish. Comparable as a full-service CDMO serving top-20 pharma with similar integrated modality breadth, though at significantly larger scale.
  • Catalent: Major global CDMO with biologics, fill-finish, and nucleic acid manufacturing capabilities. Comparable in offering CDMO services across biologics modalities and serving large pharma; differs in its broader oral and softgel specialty franchise.
  • Fujifilm Diosynth Biotechnologies: Large CDMO offering microbial and mammalian biologics, gene therapy, and vaccines manufacturing. Comparable in integrated biologics CDMO services with microbial fermentation expertise; larger scale and broader global footprint.
  • WuXi Biologics: World's largest biologics CDMO with end-to-end microbial and mammalian services, including mRNA. Comparable CDMO offering across biologics modalities and top-20 pharma clients; significant pricing pressure on North American CDMOs.
  • Samsung Biologics: Large-scale biologics CDMO with substantial mammalian cell culture capacity. Comparable in serving top-20 pharma with biologics manufacturing, but at much larger scale with different geographic footprint.

Direct peers

  • AGC Biologics: Mid-to-large CDMO specializing in microbial and mammalian biologics, gene therapy, and mRNA manufacturing. Directly comparable to BioVectra in microbial fermentation focus and CDMO service model for biologics and nucleic acids.
  • Recipharm: European-based CDMO offering biologics, fill-finish, and small molecule API manufacturing. Comparable as a full-service CDMO with similar project-based revenue model serving pharma clients, though with different geographic footprint.
  • Rentschler Biopharma: CDMO specializing in microbial and mammalian cell culture-based biopharmaceuticals with aseptic fill-finish. Directly comparable to BioVectra's biologics core, with similar mid-tier scale and European-headquartered operations.
  • Eurofins CDMO: European CDMO offering biologics, small molecule API, and HPAPI manufacturing services. Comparable as a mid-tier integrated CDMO with similar modality breadth and project-based revenue model.
  • ten23 health: Swiss CDMO specializing in sterile injectable fill-finish and biologics manufacturing for challenging modalities. Comparable in aseptic fill-finish and biologics capabilities, particularly for small-to-mid-sized pharma clients seeking specialized services.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat6 records

Customer concentration

BioVectra social profiles

Digital presence

BioVectra financial estimates

Financial estimate

Revenue estimate

Valuation estimate

BioVectra leadership team

Management profile

Number of profiles

Profiles12 records

BioVectra funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors2 records

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

BioVectra 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 BioVectra

What does BioVectra do?

BioVectra is a full-service Contract Development and Manufacturing Organization (CDMO) providing clinical-to-commercial scale production of biologics, synthetic small molecules, plasmid DNA/mRNA, lipid nanoparticles (LNP), highly potent APIs (HPAPIs), bioreagents, and aseptic fill-finished drug products. The company operates five GMP manufacturing facilities across Atlantic Canada, leveraging microbial fermentation, mammalian cell culture, synthetic chemistry, and sterile fill-finish capabilities to serve global pharmaceutical and biotechnology clients.

Is BioVectra a public or private company?

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

When was BioVectra founded?

BioVectra was founded in 1970. It employs 501 to 1,000 people.

Where is BioVectra based?

BioVectra is headquartered in Charlottetown, Canada, in the North America region.

How does BioVectra make money?

One revenue line is on record: contract Manufacturing Services.

Who are BioVectra's main competitors?

Broad incumbents on record are Lonza Group, Catalent, Fujifilm Diosynth Biotechnologies, WuXi Biologics and Samsung Biologics. Direct peers are AGC Biologics, Recipharm, Rentschler Biopharma, Eurofins CDMO and ten23 health.

Does BioVectra have an API?

No public API is recorded for BioVectra.

What industry is BioVectra in?

BioVectra's product category is Pharmaceutical Contract Manufacturing. Its primary akta.pro industry code is HLAGABAC, Biologics (mAbs/Recombinant Proteins) CDMO, with a secondary code of HLAGAGAC, mRNA & Nucleic Acid Manufacturing Services (mRNA/saRNA/Plasmid DNA). Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
EntrevestorEntrevestorPEI BioAlliance CEO Lauren Ledwell is leading a strategic review to boost the island's life sciences revenue from $634 million in 2024 to $1 billion by 2030. The plan emphasizes private investment, infrastructure like the $50 million BioAccelerator, and regional collaboration.GlobeNewswiremRNA Therapeutics CDMO Market Analysis Report 2026: $8.25+ Bn Opportunities, Trends, Competitive Landscape, Strategies, and Forecasts, 2020-2025, 2025-2030F, 2035FResearchAndMarkets.com announced the release of an mRNA therapeutics CDMO market report projecting growth from $4.74 billion in 2025 to $5.31 billion in 2026, reaching $8.26 billion by 2030 at an 11.7% CAGR, driven by infectious disease outbreaks, cancer immunotherapy demand, and LNP formulation advancements. Agilent Technologies acquired BIOVECTRA for $925 million in September 2024 to strengthen its mRNA therapeutics CDMO capabilities, while Esphera SynBio Inc. launched an LNP/mRNA vaccine enhancement project in January 2025. North America led the market in 2025, with Asia-Pacific projected as the fastest-growing region, though tariffs are increasing costs for imported raw materials used in plasmid DNA manufacturing and fill-finish services.BioPharm InternationalWeighing the Benefits of Fermentation for New BiotherapiesIndustry experts discuss the advantages and challenges of microbial fermentation in biomanufacturing for biologics production, noting that while fermentation offers lower costs, faster processing times (1-3 days versus weeks for mammalian culture), and less contamination risk, it has limitations with post-translational modifications such as glycosylation. The article explores how fermentation is used for products including insulin, human growth hormone, enzymes, and monoclonal antibodies, and its potential role in biosimilars and emerging therapies like mRNA vaccines and gene therapies. Experts from BioVectra and Ginkgo Bioworks comment on equipment considerations, including single-use versus stainless-steel fermenters, and how advances in microbial engineering may expand fermentation's applicability to more complex biologics.Nova One AdvisorGene Editing Market Size to Worth Around USD 47.34 Bn by 2035The global gene editing market is projected to grow from USD 11.29 billion in 2025 to approximately USD 47.34 billion by 2035, expanding at a compound annual growth rate of 15.41%. Key growth drivers include rising demand for advanced therapies treating genetic disorders and cancers, technological advancements in CRISPR and AI-assisted genomic tools, and increasing adoption in regenerative medicine, agriculture, and veterinary sciences. The market report also highlights recent strategic transactions such as Agilent Technologies' acquisition of BIOVECTRA in July 2024 and Merck KGaA's acquisition of Mirus Bio in May 2024 as indicators of intensifying industry consolidation and partnership activity.BioSpaceAgilent Launches Agilent Advanced Therapeutics, Unifying CDMO Capabilities Across Canada and United StatesAgilent Technologies announced the launch of Agilent Advanced Therapeutics, a unified Contract Development and Manufacturing Organization (CDMO) platform that integrates its Canadian operations (BIOVECTRA) and U.S. operations (Nucleic Acid Solutions in Colorado) to offer comprehensive end-to-end manufacturing services for the pharmaceutical and biotech industries. The integrated platform covers oligonucleotides, microbial fermentation, complex chemistry, bioreagents, highly potent APIs, and cell line development, providing customers streamlined access to a single partner from discovery through commercial-scale manufacturing. CEO Padraig McDonnell stated the launch reinforces Agilent's long-term commitment to growth, investment, and leadership in advanced therapeutics manufacturing.Stock TitanAgilent launches Advanced Therapeutics CDMO platformAgilent Technologies announced the launch of Agilent Advanced Therapeutics, a unified Contract Development and Manufacturing Organization (CDMO) platform that integrates its capabilities from BIOVECTRA in Canada and Nucleic Acid Solutions in Colorado. The platform provides end-to-end manufacturing services including oligonucleotides, microbial fermentation, complex chemistry, bioreagents, highly potent APIs, and cell line development for pharmaceutical and biotech customers. Agilent President and CEO Padraig McDonnell stated the launch reinforces the company's long-term commitment to growth, investment, and leadership in the therapeutics manufacturing space.YahooAgilent Launches Agilent Advanced Therapeutics, Unifying CDMO Capabilities Across Canada and United StatesAgilent Technologies announced the launch of Agilent Advanced Therapeutics, a unified Contract Development and Manufacturing Organization (CDMO) platform integrating its Canadian and U.S. operations. The platform combines BIOVECTRA in Canada and Nucleic Acid Solutions in Colorado to offer end-to-end manufacturing services including oligonucleotides, microbial fermentation, complex chemistry, and highly potent APIs. CEO Padraig McDonnell stated the launch strengthens customer support and reinforces the company's long-term commitment to growth and leadership in the therapeutics manufacturing space.Investing.comAgilent launches unified CDMO business combining US, Canada units By Investing.comAgilent Technologies launched Agilent Advanced Therapeutics, a unified contract development and manufacturing operations business combining its BIOVECTRA facility in Canada and Nucleic Acid Solutions in Colorado. The new division offers oligonucleotide production, microbial fermentation, synthetic chemistry, and other pharmaceutical manufacturing services spanning early-stage discovery through commercial-scale production. CEO Padraig McDonnell stated the launch reinforces the company's long-term commitment to growth and leadership in this sector.MarketsandMarketsOligonucleotide CDMO Market Growth, Drivers, and OpportunitiesMarketsandMarkets has published a global oligonucleotide CDMO market research report projecting the market to reach USD 6.73 billion by 2029 from USD 2.51 billion in 2024, growing at a CAGR of 21.8%, driven by rising demand for oligonucleotide-based therapeutics and increasing outsourcing trends. North America accounted for a 43.1% revenue share in 2023, with contract manufacturing services and therapeutic applications dominating their respective segments. Key recent developments include Agilent's USD 925 million acquisition of BioVectra (July 2024), Hongene Biotech's licensing deal with UMass Chan Medical School (September 2025), Cohance Lifesciences' USD 2.8 million facility investment in Hyderabad (August 2025), and Sumitomo Chemical's establishment of a new US-based CRO (April 2025).BiovectraBIOVECTRA and Revolution Biomanufacturing Partner to Deliver Integrated mRNA Design and GMP Production Services — Partnership Combines Sequence Design Expertise with End-to-End GMP Manufacturing to StBIOVECTRA, a subsidiary of Agilent Technologies, and Revolution Biomanufacturing announced a partnership to provide integrated mRNA design and GMP production services. The collaboration combines Revolution's proprietary sequence optimization technologies with BIOVECTRA's end-to-end manufacturing capabilities to streamline the development of mRNA therapeutics. This alliance aims to offer sponsors a seamless workflow from sequence design through sterile drug product manufacturing.