Breaking
Friday, July 24, 2026

CDMO & Manufacturing

Contract development and manufacturing partners for drug substance and product.

140 suppliers in this category · Page 4 of 6

Request directory help →

All CDMO & Manufacturing suppliers

Malvern Panalytical

Life Science Reagents

Malvern Panalytical is a Spectris-owned global manufacturer of analytical instruments used across pharma R&D, QC and manufacturing. Its portfolio spans particle size, zeta potential, XRD, XRF, BET surface area, gas pycnometry and moisture analysis, supporting decision-making from discovery through commercial production.

MaxCyte

CDMO & Manufacturing

MaxCyte is a public life-science technology company providing non-viral ExPERT electroporation systems and SeQure gene-editing risk assessment services for cell and gene therapy, biologics, and vaccine programs. Its scalable platform supports workflows from high-throughput discovery to GMP-compliant manufacturing. Headquartered in Rockville, Maryland, MaxCyte works through a partnership-driven licensing model that combines instruments with scientific, technical, and regulatory support.

MilliporeSigma

CDMO & Manufacturing

MilliporeSigma is the U.S. and Canada life science business of Merck KGaA, Darmstadt, Germany, supplying a broad portfolio of products and services for pharma research, development, and manufacturing. It combines catalog reagents and bioprocess solutions with integrated CDMO, contract testing, and consultative services to support customers from discovery through commercial production.

Miltenyi Biotec

Life Science Reagents

Miltenyi Biotec is a global biotechnology company headquartered in Bergisch Gladbach, Germany, specializing in magnetic cell separation (MACS), life science reagents, and instruments for cell and gene therapy workflows. Through its Miltenyi Bioindustry division, it also provides CDMO services for cell‑based therapies and lentiviral vectors from preclinical to commercial scale.

TriLink BioTechnologies

CDMO & Manufacturing

TriLink BioTechnologies is a San Diego–based nucleic acid and mRNA CDMO specializing in modified nucleic acids, CleanCap® capping technologies and custom mRNA solutions for research, diagnostics and therapeutics. Its offerings span IVT kits, catalog mRNAs, custom oligos, guide RNAs, mRNA CDMO services, analytical support and custom NTP synthesis with scalable GMP manufacturing.

Multiply Labs

CDMO & Manufacturing

Multiply Labs builds robotic biomanufacturing infrastructure for advanced therapies, especially cell and gene therapy. Its closed, modular automation platform is designed to increase throughput, lower costs, and integrate with existing GMP instruments and quality systems.

Nanoencapsulation Manufacturing Equipment

CDMO & Manufacturing

Leon-nanodrugs GmbH (LEON) is a Germany-based pharmatech company that develops FR-JET® mixer-based NANO® equipment for nanoparticle manufacturing from R&D to GMP. Its NANOscreen®, NANOlab®, NANOme® and NANOus® systems, combined with formulation and process development services and flexible leasing, help pharma, biotech, and CDMOs scale lipid nanoparticle and other nanomedicine processes efficiently.

Nanoworx - Home

CRO & Clinical Services

Nanoworx is a Netherlands-based CRO specializing in advanced nanomedicine development. It offers nanoparticle design, high-throughput screening, scale-up, manufacturing, and in vitro characterization for academic and industry clients.

Next generation of nanomedicine therapy

CDMO & Manufacturing

EXO Biologics is a Belgian clinical-stage biotech developing exosome-based nanomedicine therapies for rare inflammatory and respiratory diseases, with a lead focus on bronchopulmonary dysplasia in preterm babies. The company combines a proprietary GMP exosome manufacturing platform, advanced drug loading and delivery technologies, and CDMO services to support both its own pipeline and external partners from research to clinical development.

Noramco

CDMO & Manufacturing

Noramco is a small-molecule API and drug substance manufacturer that has been acquired and integrated into the Siegfried Group’s CDMO network. Its former operations now function as Siegfried drug substance sites in the US and Australia, contributing high-quality small-molecule capacity and reliable API supply for pharmaceutical customers.

Noramco

CDMO & Manufacturing

Noramco is a small‑molecule API and drug‑substance specialist that has been acquired and integrated into the Siegfried Group, a global CDMO. Its former operations and capabilities now operate under Siegfried’s API and CDMO platform, and buyers should source Noramco’s legacy offerings via Siegfried.

Obatala Sciences

CDMO & Manufacturing

Obatala Sciences is a New Orleans life-science supplier founded in 2017, focused on human-derived research tools for obesity, diabetes, cancer, regenerative medicine, and tissue engineering. Its offering includes ObaCell organ-on-a-chip platforms, ObaGel human-derived hydrogels, diverse stem cell products, specialized culture media, and contract research services for industry, academia, and government labs.

Aqdot

CDMO & Manufacturing

Aqdot is a Cambridge-based supramolecular chemtech company offering AqFresh™, a patented cucurbituril technology that captures and removes odours and VOCs from nonwovens, textiles, plastics and liquids. Its drop-in, fragrance-free solutions help manufacturers improve indoor air quality, human health and sustainability across hygiene, personal care, home care and automotive applications.

Aqdot

CDMO & Manufacturing

Aqdot is a Cambridge-based supramolecular chemtech company specialising in patented AqFresh™ odour and VOC elimination technology for nonwovens, textiles, plastics and liquids. Its drop-in solutions help manufacturers improve indoor air quality, reduce biocides and sensitising fragrances, and support sustainable production across hygiene, home care, automotive and life science applications.

Oligonucleotide & mRNA Manufacturing CMO

CDMO & Manufacturing

BioSpring is a specialized nucleic acid CDMO delivering GMP manufacturing and analytical services for oligonucleotides and mRNA from research through commercial supply. The company offers multi-grade nucleic acid drug substance and drug product manufacturing, advanced analytics, and integrated project and regulatory support, focused on ASOs, siRNA, guide RNA, mRNA and other oligonucleotides.

Openshelf

CDMO & Manufacturing

Openshelf is a New York–based robotics company that automates lab and pharmacy inventory using its open source LB AR/RS automated storage and retrieval system. The modular platform handles well plates, bottles, and other lab items, integrates with inventory systems via HTTP API, and includes barcode, labeling, and weighing capabilities for traceable, efficient storage and retrieval.

Opentrons Labworks Inc

CDMO & Manufacturing

Opentrons Labworks Inc is a private biotechnology and lab automation company that provides flexible, AI-enabled liquid-handling robots, software, and application workstations for NGS, PCR, proteomics, and nucleic acid extraction. Its open, modular ecosystem combines no-code tools, a Python API, and an extensive protocol library to help labs automate repetitive workflows while maintaining control over assays, instruments, and AI tools.

OrganaBio

CDMO & Manufacturing

OrganaBio is an FDA-registered, privately held CTDMO headquartered in Miami, Florida, providing human cellular starting materials and cGMP manufacturing for cell and gene therapy developers. With coast-to-coast ISO 7 facilities, the company supplies leukopaks, PBMCs, MSCs, HSCs and delivers clinical cell processing, cryopreservation, analytical testing, and contract manufacturing services under a unified quality system.

Ori Biotech

CDMO & Manufacturing

Ori Biotech (Oribiotech Ltd) is a CGT manufacturing technology company offering the IRO® Platform, a fully automated, closed, digital system for cell and gene therapy production. IRO® combines novel bioreactors, the Ori Connect™ sterile connection system, consumables and cloud software to improve biological performance, cut labor and costs, and scale manufacturing from R&D to GMP.

PEAK Scientific

CDMO & Manufacturing

PEAK Scientific is a privately held UK manufacturer of laboratory gas generators for pharma and analytical labs. It supplies nitrogen, hydrogen, air, and liquid nitrogen systems with global service coverage for LC-MS, GC, and GC-MS workflows.

Paragon Medical

CDMO & Manufacturing

Paragon Medical is an integrated medical device manufacturing partner offering design, development, rapid prototyping, verification and validation, and high‑precision manufacturing through to finishing, assembly, and packaging. With over a century of experience and 1.2 million square feet of global operations, it supports components and complete devices across orthopedic, minimally invasive, and other advanced medical technologies for OEMs and innovators.

Pbd

CDMO & Manufacturing

PBD Biotech is a diagnostics company developing proprietary phage-based assays and qPCR kits for rapid detection of tuberculosis and other mycobacterial infections from blood. Its lead technology, Actiphage, is designed to identify live mycobacteria and people at risk of TB progression, supported by patents and clinical trials. The company targets clinical, public health and research users seeking advanced TB diagnostic tools.

Peristaltic Pumps

CDMO & Manufacturing

Watson-Marlow Fluid Technology Solutions (WMFTS) is a leading manufacturer of peristaltic pumps and fluid-path technologies used in life sciences, pharma, biotech, and process industries. Its Watson-Marlow pump ranges provide sterile, low-shear, contamination-free fluid handling from lab to production scale, supported by specialized tubing, validation resources, and global applications expertise.

Pharmaceutical

CDMO & Manufacturing

Emerson provides integrated automation, measurement, and control solutions tailored to pharmaceutical manufacturing, from lab development to commercial scale. Its portfolio covers reaction control, purification, PAT, electronic records, and real-time equipment health, helping manufacturers improve yields, quality, and compliance while shortening time to market.

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

← Back to Supplier Hub · A–Z directory