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CDMO & Manufacturing

Contract development and manufacturing partners for drug substance and product.

140 suppliers in this category · Page 6 of 6

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All CDMO & Manufacturing suppliers

Spaceship.com

Life Science Reagents

ProteoNic is a Leiden-based biotech company founded in 2006, specializing in vector and transposon technologies for enhanced recombinant protein production. Its 2G UNic platform delivers 2-5x higher yields in CHO/HEK systems, with additional offerings for gene therapy viral vectors and glycoengineering.

Porvair Sciences

CRO & Clinical Services

Porvair Sciences Limited is the Laboratory Division company of Porvair plc, specialising in microplates, porous plastics and microplate handling instruments for life science and analytical laboratories. From high-quality plates and seals to evaporators, robotic-compatible equipment, custom manufacturing and OEM services, it supports high-throughput, reproducible sample preparation and analysis for pharma, biotech and diagnostic customers.

Synthego

Life Science Reagents

Synthego is a CRISPR and molecular diagnostics solutions provider offering guide RNAs, engineered nucleases, base editors and molecular biology reagents for research and clinical workflows. With GMP manufacturing, IND submission support and global distribution, it serves pharma, biotech and diagnostic developers building cell and gene therapies and advanced infectious disease assays.

Takara Bio—Home

Life Science Reagents

Takara Bio is a global biotechnology group that provides life science reagents, instruments, and CDMO services supporting gene, cell, and regenerative medicine research and development. Headquartered in Japan with major operations in San Jose, California, it enables pharma, biotech, and academic customers to advance biologics, cell and gene therapy, and other advanced modalities from discovery through process development and manufacturing.

Terrapinn - Spark Something

CDMO & Manufacturing

Terrapinn is a global events organizer that runs industry-specific conferences and exhibitions across health, life sciences, technology and other sectors. With offices in London, Dubai, Singapore and Sydney, it curates events such as vaccines, orphan drugs and advanced therapies congresses to connect pharma and biotech leaders with innovators, suppliers and partners.

Terumo Blood And Cell Technologies

CDMO & Manufacturing

Terumo Blood and Cell Technologies is a global medical technology company specializing in blood component processing, therapeutic apheresis, and cell therapy technologies. Serving hospitals, blood and plasma centers, and cell therapy developers worldwide, it provides systems and services that support blood collection, plasma operations, and scalable cell and gene therapy manufacturing.

Testa Analytical Solutions Ek

CDMO & Manufacturing

TESTA Analytical Solutions e.K is a Berlin‑based manufacturer and supplier of high‑performance HPLC and GPC/SEC instruments, detectors and non‑invasive flowmeters. The company focuses on polymer and particle characterization, offering viscometer/DRI combined detectors, rapid‑scanning UV detectors, DRI kits and real‑time flow monitoring solutions for chromatography labs, OEMs and service engineers.

Touchlight

CDMO & Manufacturing

Touchlight is a UK-based private CDMO specialising in high‑purity, cell‑free enzymatic DNA manufacturing for genetic medicines. Using its proprietary dbDNA™, z‑dbDNA™ and mbDNA™ platforms and a GMP‑licensed facility, it supplies RUO and GMP DNA for applications including mRNA, viral vectors, gene editing, DNA vaccines and non‑viral gene therapies, with custom manufacturing across discovery, R&D, SMart GMP and GMP scales.

Tq Therapeutics

CDMO & Manufacturing

TQ Therapeutics GmbH is a biotechnology company in Planegg/Martinsried, Germany, developing the CELLfinity platform and EXiVO extracorporeal in vivo approach for safe autologous in vivo cell and gene therapies. The company focuses on decentralized, automated processing to deliver individualized mRNA T-cell therapies and collaborates with partners to integrate its technology into scalable, point-of-care cell therapy workflows.

Trenchant Biosystems

CDMO & Manufacturing

Trenchant Biosystems is a private US biotech company developing fully automated, end‑to‑end platforms to manufacture CAR‑T and other gene‑modified cell therapies in about 2.5 days. Launched in 2022 and based in San Diego with a Sacramento mailing address, it is advancing its AutoCell platform toward early access and commercial launch to help biopharma and CDMOs scale cell therapy manufacturing while reducing costs.

UniteLabs

CDMO & Manufacturing

UniteLabs is a private lab automation software company offering a Python-based operating system for connected labs, with 175+ device connections and API-driven orchestration. It is aimed at biotech and pharma teams that want portable, versioned, auditable workflows across instruments, LIMS, and ELN systems.

Veon Scientific

CDMO & Manufacturing

Veon Scientific is a Bedford, UK-based manufacturer of compact, open-architecture liquid handling platforms, led by its i.prep 2 multi-channel instrument for lab automation. i.prep 2 combines independent channels, a configurable deck and an open control stack (REST, WebSocket, Python SDK) in a bench-top, biosafety cabinet-compatible footprint, supported by case studies, protocol libraries and ISO 9001:2015-certified operations.

Viral Vector CDMO for Gene Therapy Manufacturing

CDMO & Manufacturing

CellVec is a certified GMP gene therapy CDMO based in Singapore, specialising in the design and GMP manufacture of custom lentiviral and retroviral vectors for translational and commercial gene therapies. Using a lentivirus-based CellVec Vector Platform and a PIC/S- and EU GMP-aligned facility, it provides process development, manufacturing, regulatory and quality services for pre-clinical and clinical viral vector programs.

WMFTS

CDMO & Manufacturing

Watson-Marlow Fluid Technology Solutions (WMFTS) is a global leader in peristaltic and niche positive displacement pumps, tubing and single‑use fluid path technologies. Its specialist brands deliver secure, accurate metering, dosing, transfer and aseptic filling solutions for pharmaceutical, biotechnology, medical device and industrial applications, supported by an international network of technical experts.

clade.pro

CDMO & Manufacturing

Clade.pro designs and builds custom life science instruments and lab automation systems for research and biotech teams. It offers end-to-end engineering support from concept and prototyping through small-batch manufacturing of tailored laboratory equipment and experimental rigs.

diaago

CRO & Clinical Services

diaago is a California-based laboratory products distributor and solutions partner for pharma, diagnostics, biotech, and research buyers. Its official site highlights stocked labware, sample management, lab automation, equipment service, and ISO 9001 certification.

eXmoor Pharma

CDMO & Manufacturing

eXmoor Pharma is a Bristol-based, full-service cell and gene therapy CDMO that unites CMC consultancy, process and analytical development, facility design and GMP manufacturing under one roof. From its 65,000 ft² Cell & Gene Therapy Centre, it supports viral vectors, autologous and allogeneic cell therapies, and RNA technologies from early strategy through clinical and commercial readiness.

etherna - mRNA-LNP delivery platforms

CDMO & Manufacturing

etherna is a private, platform-driven RNA and LNP technology company offering integrated RNA chemistry, LNP delivery platforms, and cGMP RNA manufacturing from Niel, Belgium. It partners with pharma and biotech via technology, product, and platform‑integrated manufacturing models to advance nucleic acid therapeutics, including clinically advanced oncology and vaccine applications.

https://www.htanalysis.com/

CDMO & Manufacturing

HT Analysis is professional analysis software from HT Instruments for visualizing and interpreting data from its electrical test and measurement devices. Paired with the HT Analysis 2 mobile app, it lets technicians access and analyze power quality and installation measurements anytime, supporting efficient diagnostics and reporting for electrical infrastructure.

https://www.quantatherapeutics.com/

CDMO & Manufacturing

Quanta Therapeutics is a clinical-stage biotech founded in 2018, developing oral small-molecule inhibitors targeting KRAS G12D and G12V mutations in RAS-driven cancers. Headquartered in South San Francisco with a site in Radnor, PA, the company leverages its proprietary SHG platform for allosteric drug discovery and has three Phase 1 programs: QTX3034, QTX3046, and QTX3544.

Frequently asked questions

What is a CDMO in biopharma?
A CDMO (contract development and manufacturing organization) provides outsourced drug development and GMP manufacturing for biopharma sponsors—from process development through commercial supply of drug substance and drug product.
What is CMO in contract manufacturing?
A CMO (contract manufacturing organization) performs GMP manufacturing for a sponsor under contract, often for a defined process or product. A CDMO adds development services such as formulation, analytical methods, and tech transfer before manufacturing.
What is API in GMP?
API (active pharmaceutical ingredient) is the therapeutically active component of a drug product. Under GMP, API manufacturing must follow validated processes, impurity controls, and regulatory filing support (e.g., DMF or CEP) appropriate to the target market.
What is the difference between a CMO and a CDMO?
A CMO typically focuses on manufacturing; a CDMO also provides development services such as formulation, analytical method development, and tech transfer. Many sponsor RFPs use the terms interchangeably—verify scope in the quality agreement.
What does an API manufacturer do?
An API manufacturer synthesizes or biologically produces the active ingredient, validates the process under GMP, and supports regulatory filings. Sponsors may use an API CDMO for clinical batches through commercial supply or split API and drug product across vendors.
What are the top cell therapy CDMOs?
Rankings vary by modality (autologous vs allogeneic), vector type, and geography. Use this directory to compare verified CGT and viral vector capabilities on enriched profiles, then validate capacity and inspection history through audits—not third-party listicles alone.
Where can I find a list of CDMO companies?
This category hub indexes published CDMO and manufacturing suppliers with structured GMP credentials, services, and sources. Filter by modality using the browse row above, then open individual profiles before issuing an RFP.
Is this a free pharma CDMO directory?
Yes—NovaPharmaNews publishes this open supplier directory with editorial buyer guides and enriched profiles. We do not charge suppliers for basic listings; profiles are compiled from official websites and public regulatory sources.
What is fill-finish CDMO services?
Fill-finish CDMOs perform sterile drug product filling, lyophilization where required, stoppering, crimping, and visual inspection under GMP—often the final step before labeled commercial supply.
What is HPAPI manufacturing?
HPAPI (highly potent API) manufacturing requires specialized containment, cleaning validation, and occupational exposure limits. CDMOs disclose OEB bands and dedicated suite strategies for cytotoxic or hormone APIs.
How do I choose a CDMO for Phase III?
Prioritize commercial-scale capacity, PPQ experience, regulatory inspection history, and stability/comparability data. Confirm fill-finish and packaging are qualified for your presentation and that the CDMO can support concurrent US and EU filings if needed.
How are suppliers in this CDMO directory curated?
Profiles are enriched from official company websites and public regulatory sources, with quality gates before publication. See our data sources and methodology page for details.

Last reviewed: · Data sources & methodology

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