We truly believe that we are the best partner of choice with our ‘Right Chemistry for a Healthier tomorrow’ at all stages – from tailor-made development methods to production in a more efficient, green and safer way, and from regulatory compliance to global commercialization. Our well-equipped R&D labs, pilot plants, and cGMP facilities at our manufacturing sites enable development, efficient technology transfer, and scale-up of New Chemical Entities (NCEs), Regulatory Starting Materials (RSMs), Intermediates, APIs, HPAPIs (up to OEB4 levels), and Peptides.

We have been helping our clients for the last 20+ years to bring their molecules to market quickly and efficiently from clinical development through commercial stage manufacturing. We have containment facilities to manufacture HPAPIs, Corticosteroids, Cytotoxic and Oncology products.

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Drawing on more than four decades of success as the manufacturing division of AbbVie, we have the depth of experience and the technical knowledge to navigate issues and deliver the innovative solutions customers need. We are much more than a CMO – we are your partner for success.

With foresight, scientific expertise, and passion we anticipate the technical and compliance challenges along the entire pharmaceutical development journey through to commercialization. We see the complete picture to deliver our customer’s vision.

With full access to global state-of-the-art facilities and world-class talent, our customers have come to depend on our service and quality to deliver real-world results.

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Headquartered in Germany, abcr GmbH provides a comprehensive catalog of high-purity compounds along with custom manufacturing and sourcing services. Their product range supports drug discovery, materials science, and advanced R&D applications. With ISO-certified quality systems and a commitment to sustainable practices, abcr is a trusted partner for research institutions and global pharma companies alike.

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With a global network and deep industry expertise, Actalent partners with organizations to provide scalable, flexible talent solutions and project-based services. Our teams support every stage of the product lifecycle, from discovery through commercialization, enabling clients to accelerate innovation and meet regulatory demands.

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Our state-of-the-art facilities and experienced R&D team enable us to support complex synthesis and scale-up projects across various therapeutic areas. We maintain strict compliance with global regulatory standards and offer flexible manufacturing capabilities.

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Agno Pharma is a fully integrated company with in-house business development, R&D, manufacturing, and regulatory compliance capabilities. Agno Pharma is your strategic CRO & CMO for drug discovery, development, and commercialization.

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AMI operates state-of-the-art, GMP-compliant manufacturing facilities and emphasizes continuous improvement and regulatory compliance. The company’s product portfolio spans therapeutic areas including anti-infectives, cardiovascular, anti-inflammatory, and central nervous system (CNS) drugs. AMI is committed to sustainable practices and long-term partnerships with customers worldwide.

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Operating eight manufacturing sites and supported by over 90 scientists and 1,700+ employees, Anupam Rasayan excels in complex molecule manufacturing and scalable production—with over 30,000 MTPA installed capacity :contentReference[oaicite:1]{index=1}.

The company’s integrated R&D and chemistry capabilities enable tailored, sustainable solutions, backed by strong ESG initiatives such as renewable energy, waste recycling, and UN Global Compact membership :contentReference[oaicite:2]{index=2}.

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Based in Poland, Apeiron Synthesis provides high-performance ruthenium-based catalysts and technical support to optimize complex chemical processes. Their catalysts are trusted by pharma and CDMO partners worldwide for improving yields, simplifying steps, and advancing sustainable chemistry. With ongoing R&D and scalable supply, Apeiron accelerates the adoption of olefin metathesis in both development and commercial manufacturing.

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Apeloa operates seven USFDA-inspected API manufacturing sites and two drug product facilities. The company supports preclinical through commercial-stage programs with capabilities in synthetic chemistry, biocatalysis, peptide synthesis, and HPAPI handling. Apeloa also maintains a U.S.-based R&D center in Billerica, Massachusetts, offering advanced support for complex molecules, including PROTACs and ADC payloads.

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Arevipharma operates a state-of-the-art, USFDA-inspected manufacturing site in Germany with more than 140 years of pharmaceutical heritage. Through its U.S. presence, Arevipharma offers direct support and streamlined access to over 30 commercial APIs and custom development services. The company specializes in complex chemistries, niche generics, and exclusive synthesis tailored to client needs.

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Operating from a single 15,000 m² site in Alnwick, England, Arcinova offers seamless project management from preclinical development through Phase II. The company provides expertise in process chemistry, radiolabeling, solid form sciences, and GMP manufacturing—enabling accelerated timelines and cost-effective development strategies.

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With cGMP-compliant facilities and a strong commitment to quality and innovation, Ascensus supports pharmaceutical customers across the drug development lifecycle—from process development to commercial production. The company offers a range of proprietary products and also provides CDMO services tailored to complex, highly specialized chemistries.

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Asymchem’s commitment to excellence and innovation has positioned it as a trusted partner in the industry. Through its advanced technologies and dedicated team, Asymchem strives to provide high-quality solutions that accelerate drug development and commercialization for clients worldwide.

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By providing access to our resources, knowledge, and experience, we create success for our clients and ultimately for patients. We offer integrated and standalone services for medicinal chemistry, biology, preclinical services, DMPK studies, development, and manufacturing for clinical phase I-III programs, regulatory submission batches, and commercial manufacturing. A differentiating factor is the integrated API and formulations service that spans from key starting material, advanced intermediates, APIs to finished products such as oral solids, sterile products, nasal solutions, etc. Our development services in India are complemented by cGMP commercial manufacturing facilities in the UK, Mexico, USA, and India.

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We collaborate with leading pharmaceutical companies and institutes, offering services such as FTE and FFS for discovery medicinal chemistry, and CDMO for the commercial manufacturing of KSMs (ISO) and registered intermediates (c-GMP). Renowned for meeting tight timelines, we support critical trials with our breakthrough scientific innovations and expediting time to market.

Our laboratories are outfitted with state-of-the-art instruments to provide reliable data crucial for decision-making. To meet client demands, we employ > 330 scientists and have expanded our R&D laboratory space to 20,000 m².

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Headquartered in Australia with expanding global operations, Boron Molecular supports pharmaceutical and biotech companies with services spanning early R&D through to GMP manufacturing. Their core strength lies in boron-based chemistry, process optimization, and scale-up of novel compounds. The company offers custom synthesis, route scouting, and development of key intermediates and APIs, serving clients across North America, Europe, and Asia.

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CatScI Ltd provides a wide range of services to enhance the efficiency and effectiveness of chemical processes. With a focus on catalysis, CatScI works with various industries to improve reaction pathways and develop sustainable processes. Their expertise extends to training and consultancy services, making them a trusted partner for both new and established clients.

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Our mission is to help make research possible. That starts by employing a talented and highly qualified group of experts to develop the tools to support research scientists across academic, biotechnology, and pharmaceutical institutions. Our scientists are experts in the synthesis, purification, and characterization of a wide range of biochemicals. We are highly skilled in all aspects of assay and antibody development and are fully accomplished at protein expression, crystallization, and structure determination.

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Founded in 1981, Chem-Impex supports pharmaceutical, biotech, and academic research with ISO-certified operations and a commitment to quality and speed. The company offers custom manufacturing services from milligram to kilogram scale and continues to expand its catalog to meet evolving research needs.

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Compared to traditional chemistry synthesis CRO services, the AI and automation platform not only improves quality consistency and delivery efficiency, but also reduces cost and provides significant ESG values via its quantitative green chemistry system.

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Chieron’s core strengths include custom synthesis, process optimization, and reliable commercial supply of complex small molecules. The company operates GMP-certified facilities and maintains a strong focus on innovation, documentation, and meeting international quality standards.

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The combined company has more than 100,000 L of manufacturing capacity, with expertise in high pressure asymmetric hydrogenation and cryogenic reactions. The company has successfully developed and scaled up many processes for the commercial manufacture of both chiral and achiral intermediates. Chiral Quest’s chiral technology portfolio combined with Long Life’s low-cost manufacturing provides a unique service offering in China.

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Backed by multiple USFDA- and EU-approved manufacturing facilities, Cohance Lifesciences serves both innovator and generic companies with end-to-end chemistry capabilities. The company operates across key therapeutic segments and emphasizes operational excellence, regulatory compliance, and sustainable manufacturing practices.

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With more than four decades of experience, Colonial Metals provides metal sales, pool accounting, and on-site refining for rhenium and ruthenium, maintaining close ties to mines and major metal suppliers to ensure supply integrity. :contentReference[oaicite:1]{index=1}

The company supports advanced manufacturing capabilities including custom synthesis, CVD/ALD/PLD precursor production, energetic beam chemical services (EBCS), and semiconductor-grade packaging under ISO cleanroom environments. :contentReference[oaicite:2]{index=2}

Its modern analytical laboratory offers R&D method development, method validation, impurity and stability testing, and advanced instrumentation (ICP-MS/OES, SEM, XRD, UV-VIS, FT-IR, and more), supporting diverse sectors from pharma to semiconductors. :contentReference[oaicite:3]{index=3}

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CordenPharma experts translate complex ideas, processes, and projects at any stage of development into high-quality products. Our integrated services support clients in bringing their products to market efficiently and reliably.

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With GMP-certified facilities in the United States and China, CPC Scientific provides a full range of services including custom peptide synthesis, peptide library production, process development, scale-up, and large-scale manufacturing. The company’s expertise spans complex modifications, peptide–drug conjugates, and therapeutic oligonucleotides, making it a trusted partner for drug discovery and development worldwide.

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Based in South Korea, Curachem serves pharmaceutical and biotech clients worldwide with advanced capabilities in 13C, 15N, 2H, and tritium labeling. The company supports projects from discovery to clinical development, including IND-enabling studies, and operates under strict quality systems with global regulatory compliance. Curachem also provides peptide synthesis and radiolabeling services for drug metabolism, pharmacokinetic, and tracer studies.

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Our capabilities include providing materials for preclinical trials or large-scale manufacturing under non-GMP and GMP conditions. With support from our expert team of analysts, chemical engineers, and QA professionals, we rapidly and efficiently develop scalable manufacturing processes to meet any need, including high-potency APIs and DEA-licensed controlled substances.

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We focus on cost-effective API syntheses, supplier backup, and technology solutions. Areas of focus include developing robust syntheses to lower API costs, backup supplier mitigation, and technology-based solutions to overcome manufacturing challenges. Our alliance partners provide services across the R&D continuum, including medicinal chemistry, in vivo studies, in vitro studies, process research, cGMP API manufacturing, RSM manufacturing, commercial manufacturing, formulation, crystallization R&D, drug product manufacturing, sourcing, generic API sourcing, GMP audits, CMC consulting, regulatory consulting, and support with licensing and fundraising activities.

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Dipharma offers high-containment capabilities, specialized technologies like hydrogenation and cryogenic reactions, and full regulatory support for global submissions. We serve clients worldwide with a strong track record in complex chemistry, sustainability, and long-term reliability.

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DOTTIKON ES manufactures high-quality intermediates and exclusive APIs, from the kilogram to the multi-ton range, for the world’s leading pharmaceutical and chemical industries. Hazardous reactions often allow to shorten production and synthetic procedures, reduce waste, improve yields, selectivity, and purity, and therefore reduce overall costs.

Among the core strengths of DOTTIKON ES are hazardous reactions, such as reductions with complex hydrides, alkylations, azide chemistry, nitrations and oxidations, as well as heterogeneous and homogeneous catalytic hydrogenations, continuous reaction technologies, and low-temperature reactions.

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Our portfolio includes dye-labeled compounds, coupling reagents, and purification media tailored to customer specifications. Headquartered in Germany with a U.S. presence, emp Biotech delivers flexible, responsive solutions to global life science clients with a commitment to quality and innovation.

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For biologics, our expertise lies in the development and scaling of monoclonal antibodies (mAbs) and other mammalian-based therapeutic proteins. Our comprehensive service offerings include testing of drug substance, final product, intermediates, and starting materials for both small and large molecule drug products.

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As a global leader in HPAPI manufacturing, we can seamlessly take your project from lab scale through to large commercial multi-ton quantities. Our global development and manufacturing network provides increased flexibility to meet your demanding requirements. At our facility in Lafayette, IN, which has been producing commercial quantities of HPAPIs for two decades, we operate with OELs <0.1 µg/m3. Evonik has experienced people with the right expertise, the right equipment, and the right motivation to see your high potency projects from clinical stages through commercialization.

Our offering also includes the manufacture of non-exclusive intermediates and APIs such as L-tert-leucine based building blocks, Lisinopril, Lorazepam, and Nifedipin. We also offer amino acids, amino acid derivatives, and small chain peptides for parenteral or oral nutrition, or as building blocks for synthesis.

For your formulation needs, Evonik produces functional excipients for modified oral delivery (EUDRAGIT®) and bioresorbable polymers for extended release parenteral formulations or medical devices (Resomer®). We offer formulation development services for both oral and injectable forms. Evonik has expertise in solubility and bioavailability enhancement of oral formulations utilizing spray drying, hot melt extrusion, and other proprietary technologies. We also have expertise in injectable extended release formulations including microsphere, gel, and implants.

Custom manufacturing services for oral drug products from preclinical to clinical phases as well as parenteral drug manufacturing from clinical through drug commercialization are also offered.

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Fareva’s capabilities span crystallization, hydrogenation, spray drying, particle size control, grinding, wet milling, and sterile micronization. With three production sites, over 100 developed chemical processes, and 800+ employees, Fareva ensures quality through regular inspections by EMA, FDA, and other agencies.

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With two state-of-the-art manufacturing facilities and advanced R&D operations—including a modern pilot-scale unit—Fermion operates entirely within Finland. The company has made significant, ongoing investments in its capabilities, particularly in the production of highly potent active pharmaceutical ingredients (HPAPIs).

All Fermion sites adhere to current Good Manufacturing Practice (cGMP) standards and uphold rigorous environmental, health, safety, and sustainability protocols. These facilities are regularly inspected by global regulatory authorities, including the U.S. Food and Drug Administration (FDA), and are frequently audited by partners and customers.

Fermion’s Contract Development and Manufacturing Organization (CDMO) services support customers from Phase I clinical trials through to commercial production. With a track record in NCE development dating back to the 1990s, Fermion has played a pivotal role in the development of approximately 15 NCEs currently marketed worldwide, including in the United States, European Union, Japan, and China.

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We provide a range of services from process development to routine production, handling quantities from grams to tons. Our services include:

• Micronization
• Milling
• Cryogenic Milling
• Sterile Micronization
• Micronization in Isolator
• Fractionated Sieving
• Homogenization & Blending
• PSD Analysis
• PSD Development, Transfer & Validation

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Located in the Gracefield Innovation Quarter in Wellington, New Zealand, we are passionate about creating life-changing drugs. Our experience in current good manufacturing practice (cGMP) means we can help you take your products from concept to the lab and into the clinic.

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Headquartered in Madrid, Grupo Juste operates USFDA and GMP-certified manufacturing facilities and offers comprehensive services including ROS design, process development and commercial supply for Human and Animal Health.

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Harman Finochem operates two advanced manufacturing sites that have been inspected by global regulatory authorities such as the USFDA, EDQM, PMDA, KFDA, TGA, ANVISA, and other PIC/S agencies. The company offers CRAMS/CDMO services including contract API and finished dosage form manufacturing—all supported by strong R&D and quality systems.

Its portfolio includes widely used APIs like Metformin HCl, Allopurinol, Fenofibrate, Divalproex Sodium, Riboflavin Phosphate, and Glycopyrrolate. The company also holds regulatory certifications such as COS/CEP, USDMFs, and EU dossiers and provides services like custom manufacturing, solid dosage, and full regulatory support.

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As a subsidiary of Heidolph Instruments GmbH, Heidolph North America supports pharmaceutical and chemical development with world-class rotary evaporators, overhead stirrers, shakers, and benchtop reactors. Known for German engineering, unmatched service, and user-friendly design, Heidolph solutions help optimize workflows from discovery through pilot scale. Their team provides dedicated application support and fast, responsive service across the U.S. and Canada.

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Operating through our two core verticals—Honour Synthesis and Honour Specialty—we embrace the science of partnership and the possibilities it creates. Our team of over 2,500 professionals collaborates closely with pharmaceutical, biotechnology, and specialty industries worldwide to develop practical, scalable solutions that make a real difference.

For more than a decade, we’ve been at the forefront of process development, custom manufacturing, and custom synthesis solutions. Our commitment to sustainability, quality, and collaboration underpins every partnership, as we work to improve everyday life and help shape a better, more advanced future.

Our state-of-the-art R&D facility, spanning 45,000 ft² and backed by over 300 scientists, empowers us to support projects from discovery through to commercialization. By combining advanced chemistry with cutting-edge technology, we provide tailored solutions that meet the unique challenges of each client.

At Honour, we’re not just transforming molecules—we’re transforming possibilities.

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Custom services and strong partnerships with clients have been a company focus since the very beginning and, thanks to a meticulous activity done over the last 30 years, nowadays those represent one of the Indena’s key strengths.

Today, Indena manufactures 12 commercial HPAPIs from different origin: synthetic, semi-synthetic and fermentation molecules. This positioning has been achieved thanks to Indena capacity to handle HPAPI with an OEL from 1 Microgram/m³ to 1 ng/m³; the onsite availability of complementary technologies such as GMP microbial fermentation/biotransformation, synthesis and extraction capabilities and its qualified and cohesive CDMO team.

Moreover, with over 30 years’ experience in the spray drying from organic solvents, Indena has expanded and upgraded its mid- and large-scale spray dryers. These represent Indena’s major technological pillars securing customized solutions to its partners.

Products and Services:
– HPAPI development & manufacturing (down to an OEL of 1 ng/m³ – OEB 6), including ADC payloads
– Fermentation of HPAPI and complex APIs
– Complex API development & manufacturing
– Chromatography services
– Spray drying from organic solvents, also in presence of excipients

Target Audience:
Indena is looking to connect with biotech and pharma companies that are looking for a CDMO partner for their HPAPIs and complex API small molecules to support for clinical trials (phase I, II and III) and commercialization.

Differentiation:
Its extensive capabilities and expertise in highly potent small molecule manufacturing. Its capacity to develop and manufacture complex small molecules irrespective of their source. Analytical expertise. State-of the art equipment and glove boxes. Commitment to start a new project within 90 days.

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With decades of R&D experience, the team is capable of pharmaceutical research on various dosage forms, leveraging key technological platforms for multiple delivery systems.

Jiuzhou Pharma’s Peptides platform provides services from preclinical pharmaceutical research to commercial manufacturing of peptide (including conjugated) APIs.

Talk to Jiuzhou Pharma about Custom Synthesis, Clinical Trial and Commercial Manufacturing, Formulation R&D/Production, AR&D, and FDA Inspected Facilities.

Molecule to Market: Your Trusted Partner. With facilities in North Carolina, USA – Germany – Japan – China.

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Services span structural biology, computational and medicinal chemistry, synthetic chemistry, in‑vitro/in‑vivo biology, DMPK, toxicology, process R&D, technology transfer, and GMP manufacturing—from preclinical through commercial stages :contentReference[oaicite:1]{index=1}.

Jubilant Biosys operates six plants, a pilot plant, kilo lab, and ~180 reactors (10 L–15,000 L), supporting small-scale to large-volume programs with a focus on quality, sustainability, and flexibility :contentReference[oaicite:2]{index=2}.

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Our expertise in the pharmaceutical sector allows us to deliver tailored solutions for small molecule synthesis, ensuring high quality and compliance with global standards.

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With decades of experience and a strong reputation for quality, Juzen Chemical provides advanced intermediates and contract manufacturing services tailored to client needs. The company specializes in complex multi-step synthesis and supports projects from early-stage development to commercial scale. Juzen maintains high standards for environmental responsibility and operates under strict quality and regulatory systems.

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Headquartered in China, JYMed operates multiple GMP-certified facilities and supports a wide range of peptide formats, including long-chain, modified, and complex peptides. The company’s services cover custom synthesis, process development, and commercial API supply, backed by strong regulatory experience in the U.S., EU, and other major markets.

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As a manufacturer, we are known for our cGMP Services for intermediates, APIs and excipients at our St. Francis, Wisconsin USA plant, and for its upstream integration with our plant at Fuxin, Liaoning China for RSMs, intermediates building blocks, specialty chemicals.

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With decades of expertise in complex multi-step synthesis, LANXESS / Saltigo offers comprehensive CDMO services from process development to commercial-scale manufacturing. The company operates state-of-the-art, cGMP-compliant facilities and is known for its excellence in handling hazardous reactions, high-potency compounds, and demanding regulatory requirements. LANXESS / Saltigo’s partnership-driven approach ensures flexibility, reliability, and top-tier quality for customers worldwide.

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LIOS offers integrated services across medicinal chemistry, custom synthesis, route development, and process optimization. With extensive expertise in heterocyclic and chiral chemistry, the institute supports pharmaceutical partners worldwide in the early development pipeline. It operates under ISO-certified systems with a strong focus on high-quality research, IP generation, and technology transfer.

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Leveraging 15 USFDA-approved facilities and a proven track record in quality and compliance, Lupin Manufacturing Solutions supports partners from clinical supply to commercial production. Its capabilities span high-potency APIs, complex oral solids, injectables, and more—making it a strategic partner for pharma companies worldwide.

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Headquartered in Himachal Pradesh, Morepen operates USFDA-approved manufacturing facilities and offers expertise in large-scale production of antihistamines, cardiovascular, anti-diabetic, and other therapeutic category APIs. The company is committed to quality, compliance, and sustainable manufacturing practices, and continues to expand its global footprint through strategic partnerships and innovation.

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For more information and to better understand what we can offer, please check our official website: [website]

Contact sales@mingchemical.com to discuss your upcoming development or manufacturing project with our experts.

We manufacture APIs and Drug Products under Drug Manufacturing License from California Department of Public Health and have passed quality audits by Merck and other major pharmaceutical companies with no observed violations.

Custom labeling, custom synthesis, custom radiolabeling, cGMP, GMP, GLP, Radiochemistry, Radiolabeling, Radiochemicals, carbon-14, C14, tritium labeling, tritiation, radiochemistry, radiosynthesis, API, active pharmaceutical ingredients, clinical trials, 3H, drug product, analysis, analytical, radio-GMP, radio-cGMP.

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In addition to formulation capabilities, we offer a Foreign Trade Zone to securely move materials into the USA, even before an IND is complete. Our comprehensive services include analytical, stability, and logistical support tailored to meet client needs.

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Our strength is our expertise in manufacturing of APIs and advanced intermediates from our US FDA approved facilities. Our core competency lies in the application of strong process chemistry to manufacturing in a regulatory compliant environment, which is supported by a strong, well-qualified team of more than 1600 employees.

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Backed by world-class R&D and manufacturing facilities in India, NFIL USA delivers complex fluorination solutions for early-stage development through to commercial supply. The company is known for its expertise in niche chemistries including halex, electrochemistry, and multi-step synthesis, serving innovators across regulated markets.

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PBL’s capabilities include clinical labeling, packaging & kitting, global distribution, returns/reconciliation, comparator sourcing, aliquoting, and secure GDP/GMP storage within its 25,000 sq ft facility—operating 24/7 with fully backup-supported systems.
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Founded in 2017 and located in the Greater San Diego area, PBL supports biotech, pharmaceutical, vaccine, and medical device clients with agile, cost-effective clinical trial logistics. It offers customized study kit designs and reliable delivery to clinical sites worldwide. :contentReference[oaicite:2]{index=2}

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The company provides a wide range of services, including formulation development, analytical testing, clinical trial manufacturing, and regulatory support. Pace operates FDA-registered, cGMP-compliant facilities and combines scientific expertise with cutting-edge technology to support both small molecule and biologic programs.

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