Oral Solid Dose CDMOs

CD Formulation

United States

CD Formulation provides formulation development, analytical services, drug packaging, and pharmaceutical excipient solutions for pharmaceutical and biotechnology companies. The company offers contract manufacturing and contract research services including liposome cGMP manufacturing, accelerated stability studies, and a wide range of formulation types including oral solid, injectable, and topical formulations. They also supply pharmaceutical excipients and active pharmaceutical ingredients.

Cenexi

Belgium

Cenexi is a Belgian/French CDMO specializing in sterile products, biological and injectable pharmaceutical manufacturing. The company operates four manufacturing sites in Europe, including sites in Fontenay-sous-Bois and Herouville-Saint-Clair (France), Osny (France, for highly active solid pharmaceutical forms), and Belgium. Cenexi offers services from development to commercial production for pre-filled syringes, vials, lyophilized products, tablets, capsules, and syrups, with FDA-registered manufacturing operations.

Chempro Pharma

India

Chempro Pharma Pvt. Ltd. is an Indian CDMO and exporter of APIs, intermediates, KSM, impurities, pellets, and finished dosage forms (FDF). The company operates WHO/EU GMP-approved facilities and is ISO 9001 certified, with manufacturing sites in Vapi, Gujarat and Maharashtra. It provides contract manufacturing services for both APIs and finished formulations.

Coating Place Inc

United States

Coating Place Inc is a Wisconsin-based pharmaceutical CDMO founded in 1976, specializing in Wurster fluid bed coating technology for oral solid dosage forms. The company operates FDA- and EMA-approved GMP facilities in Verona and Sauk City, Wisconsin, with 24 proprietary Wurster fluid bed coaters handling batches from 0.010 kg to 800 kg, and is DEA-licensed for Schedule I-V controlled substances. The company celebrated its 50th anniversary in 2026.

Codis

United States

Codis is a global CDMO specializing in commercial-scale spray drying, amorphous solid dispersions (ASD), and particle engineering technologies. Formed through the integration of Particle Dynamics in the US and the Haverhill, UK facility previously operated by EUROAPI, the company operates over 400,000 sq ft of cGMP manufacturing space across three sites with a 30-year regulatory track record, and is the world's leading manufacturer of Sevelamer API producing hundreds of metric tons annually.

Confab Laboratories

Canada

Confab Laboratories is a well-established CDMO located on Montreal's South Shore, Canada, specializing in non-sterile pharmaceutical manufacturing of liquid, solid, and semi-solid dosage forms. The company provides end-to-end services including formulation development, technology transfer, analytical services, and commercial manufacturing for prescription, OTC, generic, controlled drugs, and veterinary products. Confab operates a 100,200 square-foot GMP facility with 32 manufacturing suites and 17 packaging suites, approved by both the FDA and Health Canada.

Contract Pharmacal Corp (CPC)

United States

Contract Pharmacal Corp (CPC) is a leading CDMO for the nutraceutical and pharmaceutical industries, headquartered in Hauppauge, New York. The company has over 50 years of experience in developing and manufacturing solid-dose OTC drugs, dietary supplements, and Rx products, with an annual capacity of 25 billion solid doses. CPC manufactures tablets, bilayered tablets, capsules, banded capsules, pellets, granules, powders, and effervescents, and partners with major brands including Tylenol, Centrum, and Breckenridge Pharmaceutical.

Contract Pharma Solution UAB

Lithuania

Contract Pharma Solution UAB is a Lithuanian contract manufacturer providing manufacturing and packaging services for dietary supplements, cosmetics, and medical devices. The company produces liquids, capsules, tablets, and powders, and offers custom formulation development, ingredient sourcing, and packaging solutions including glass bottles, plastic bottles, sticks, blisters, and cartons. CPS is ISO 22000, ISO 13485, and GMP certified, serving over 100 clients in 15+ countries.

CorePharma LLC

United States

CorePharma LLC, founded in 1998 and headquartered in Middlesex, NJ, is a CDMO specializing in oral solid dosage forms including IR and ER tablets and capsules. The company offers end-to-end services from product development and contract manufacturing to packaging and analytical testing, with cGMP-compliant FDA & DEA registered facilities producing over 2 billion units annually.

CRAMSN Research Park

India

CRAMSN Research Park is an India-based contract research, development, and manufacturing organization offering end-to-end CRO, CDMO, and CMO solutions. The company provides drug substance (API) and drug product manufacturing with multiple facilities in India and a facility in New Jersey, USA, committed to sustainable practices including green chemistry and solar-powered operations.

Crystal Pharmatech

Canada

Crystal Pharmatech is a global pharmaceutical CRO/CDMO headquartered in Canada specializing in solid-state research, advanced formulation development, and GMP manufacturing for small molecule drugs. The company offers a First-Time-Right 3-STEP approach from API form selection through crystallization development to clinical and commercial manufacturing, with sites in Canada, the US, and China.

Custom Pharma Services

United Kingdom

Custom Pharma Services is a UK-based CDMO founded in 1979 in Brighton, specializing in oral solid dose manufacturing and packaging for clinical and commercial use. The company is MHRA-approved and FDA-inspected, with capacity exceeding 1.5 billion tablets and 250 million capsules annually. Custom Pharma handles controlled drugs, hormonal products, and has launched Centrix Pharma Solutions for early-stage development.

Danhson

Bulgaria

Danhson is a Bulgaria-based pharmaceutical holding company established in 2015, with group companies including Vetprom AD (65+ years of manufacturing history) and Danapha Pharmaceutical in Vietnam. The company develops, produces, and markets pharmaceutical products (Rx and OTC), food supplements, and cosmetics, with CMO/CDMO services. Danhson has invested BGN 50 million in a new production site with separate workshops for ampoule forms, liquid forms, semisolid, and biological products.

Davipharm

Vietnam

Davipharm (Dat Vi Phu Pharmaceutical JSC) is a Vietnamese pharmaceutical manufacturer and member of the Adamed group, holding EU GMP certification. The company manufactures over 300 generic drug products at its facility in Binh Duong, Vietnam, and offers CMO/CDMO services including high-potency drug manufacturing. Davipharm recently expanded its capacity and capabilities in high-potency manufacturing.

Delpharm

Canada

Delpharm is one of the world's top five CDMOs, specializing in the development and manufacture of medicines across solid, sterile, semi-solid, and liquid dosage forms with particular expertise in nasal sprays and injectables. The company operates 18 manufacturing sites and 3 development centers across Europe and North America, with 6,500 employees and over 1.1 billion EUR in turnover. Delpharm produces over 650 million units annually and recently received a $60 million Canadian government investment to modernize its Boucherville injectable facility.

DifGen Pharmaceuticals

United States

DifGen Pharmaceuticals is a US-based CDMO specializing in complex generics and advanced drug delivery systems, providing end-to-end solutions from product development through commercial manufacturing. Through its 2023 acquisition of Aveva Drug Delivery Systems Inc., DifGen gained a 455,000 sq. ft. US manufacturing footprint producing over 300 million transdermal patches annually, including controlled substances like buprenorphine transdermal systems.

Emil Pharmaceutical Industries Pvt Ltd

India

Emil Pharmaceutical Industries Pvt. Ltd. is an Indian CDMO founded in 1989, headquartered in Mumbai with three manufacturing units in MIDC Tarapur, Maharashtra. The company manufactures pharmaceuticals, nutraceuticals, and OTC formulations including tablets, capsules, powders, liquids, creams, and ointments. Emil has partnered as a CDMO with global companies including Abbott, Mylan, Pfizer, GSK, USV, and MSD, and exports to over 25 countries with certifications from WHO, ISO 9001, NAFDAC Nigeria, and FDA Ghana.

Fisher BioServices (Thermo Fisher)

Netherlands

Fisher BioServices is part of Thermo Fisher Scientific's Patheon pharma services division, one of the world's largest CDMOs offering end-to-end 360-degree CDMO and CRO solutions. The Patheon platform covers drug substance and drug product manufacturing for small molecules, large molecules, and advanced therapies, along with clinical supply and commercialization services.

Galenicum Health

Spain

Galenicum Health is a Spanish specialty pharmaceutical company founded in 2003 in Barcelona, operating as a CDMO with a manufacturing facility near Madrid. The company produces finished dosage forms in multiple formats including liquids, ointments, creams, sachets, powders, nasal sprays, tablets, and capsules, with a production capacity of over 50 million packs per year. Galenicum operates in 58+ countries with 800+ employees and consolidated revenues of 213M EUR (2023).

Glenmark (incl. API arm Glenmark Life Sciences)

Argentina

Glenmark Pharmaceuticals is a global innovation-driven pharmaceutical company focused on branded and generic formulations, with an API manufacturing arm called Glenmark Life Sciences. The company manufactures APIs and finished dosage forms primarily for its own portfolio, spanning dermatology, respiratory, oncology, and cardiovascular therapeutic areas. Glenmark Life Sciences produces over 120 APIs across multiple manufacturing sites in India.

Global Pharma HealthCare (India)

India

Global Pharma HealthCare is an Indian pharmaceutical CDMO offering contract development and manufacturing services for sterile and non-sterile dosage forms. The company provides end-to-end services from formulation development through commercial manufacturing, including oral solids, liquids, sterile injectables, and lyophilized products. It serves regulated markets including the US, EU, and other global markets.

Globela Pharma Pvt Ltd

India

Globela Pharma Pvt Ltd is an Indian pharmaceutical company founded in 2006, offering CDMO, CRAMS, and API manufacturing services. The company has specialized EU GMP-certified facilities for oncology (cytotoxic) and cephalosporin manufacturing, with a DSIR-approved R&D center and exports to over 50 countries. It provides end-to-end services from API and intermediate manufacturing through finished dosage form production.

Goodwill Pharma PLC

Hungary

Goodwill Pharma PLC is a Hungarian pharmaceutical company founded in 1997 that develops, manufactures, and distributes medicines and dietary supplements across Central and Eastern Europe. The company explicitly offers CDMO services covering early-stage development through commercial manufacturing, with GMP-licensed production facilities. It operates in 12+ countries with 200+ products and 300+ employees.

Granules (Granules India)

India

Granules India Limited is a vertically integrated pharmaceutical company and CDMO specializing in high-volume oral solid dosage manufacturing from APIs through finished dosage forms. The company is one of the largest manufacturers of core molecules such as paracetamol, metformin, guaifenesin, and ibuprofen, operating multiple FDA- and EU GMP-approved manufacturing facilities across India and the US. It provides contract manufacturing services for global pharmaceutical companies.

H C CLOVER PRODUCTOS Y SERVICIOS SL (Clovert y / Cloverty)

Spain

Cloverty (formerly HC Clover PS) is a Spanish pharmaceutical CDMO specializing in soft gelatin capsules. The company also develops and manufactures products in various dosage forms including hard capsules, sachets, sticks, ampoules, and vials, with primary and secondary packaging capabilities.

Hebei Yiyang Jingcheng Technology Co., Ltd

China

Hebei Yiyang Jingcheng Technology Co., Ltd (Yiyang Pharma) is a full-service contract manufacturer with facilities and warehouses in China, Canada, and Italy. Formerly a pharmaceutical factory, the company produces tablets, capsules, softgels, gummies, beverages, and oral dissolving films, certified by ISO, BRC, US FDA, NSF, cGMP, and Health Canada.

Helba İlaç İç ve Dış San. Tic. A.Ş.

Turkey

Helba Pharma is a Turkish pharmaceutical manufacturer established in 2008, with roots in Welfar Pharma founded in Azerbaijan in 1995. The company produces solid and semi-solid form medicines at its GMP-certified production facility with 50 million box manufacturing capacity, and actively exports to CIS countries, Balkans, and Middle Eastern markets.

Help S.A. (HELP Pharmaceuticals)

Greece

HELP Pharmaceuticals is a Greek pharmaceutical company founded in 1971, operating an EU-GMP certified production facility in Ioannina, Greece. The company manufactures pharmaceuticals, medical devices, nutraceuticals, and cosmeceuticals across sterile and non-sterile lines, including solid, liquid, and semi-solid dosage forms. HELP serves partners in more than 50 countries and provides clinical manufacturing and packaging services.

HERMES PHARMA

Austria

HERMES PHARMA is an Austrian CDMO and the leading expert in developing and manufacturing user-friendly oral dosage forms. A sister company of HERMES Arzneimittel (100+ years of pharmaceutical excellence), HERMES PHARMA offers a one-stop-shop from product design through GMP manufacturing. The company recently announced a 25 million euro investment to expand oral drug production capabilities. Their dosage form portfolio includes effervescent tablets, chewable tablets, orally disintegrating granules, instant drinks, and lozenges.

Hovid Bhd

Malaysia

Hovid Bhd is a Malaysia-based pharmaceutical company with over 80 years of history, operating as both a branded generic producer and contract manufacturer. The company offers a portfolio of over 400 products including generic drugs, OTC supplements, disinfectant solutions, medical devices, and consumer products, with distribution in more than 50 countries.

Hovione

China

Hovione is a specialist integrated CDMO dedicated to helping pharmaceutical customers bring new and off-patent drugs to market. Founded in 1959, the company provides API development and manufacturing, drug product development, and particle engineering services across four GMP manufacturing sites worldwide.

Iberfar – Industria Farmaceutica, S.A.

Portugal

Iberfar, Industria Farmaceutica, S.A. is a privately owned Portuguese pharmaceutical contract manufacturer founded in 1924. The company specializes in contract manufacturing of solid forms and non-sterile liquid products, including controlled drugs, at its EU cGMP-certified facility near Lisbon.

Importfab Inc

Canada

Importfab Inc (now Labomar Canada) is a well-established Canadian contract manufacturer acquired by Labomar S.p.A., a leading Italian CDMO. The company specializes in manufacturing pharmaceuticals, natural health products, cosmetics, nutraceuticals, and veterinary products. It recently completed an FDA audit and expanded its headquarters facility in Montreal.

Ind-Swift

India

Ind-Swift Laboratories Ltd., established in 1995 and headquartered in Chandigarh, India, is a leading API manufacturer and CDMO providing contract research and manufacturing services (CRAMS). The company operates multi-locational cGMP manufacturing facilities in Punjab with 22 manufacturing blocks and additional capacity in Jammu, producing APIs and oral solid dosage forms including tablets, hard gelatin capsules, and soft gelatin capsules.

InnoGenerics

Netherlands

InnoGenerics was the largest Dutch generics manufacturer, producing three billion pills per year before going into bankruptcy. The company was subsequently acquired by Ofichem and restarted as Ofimedicine, continuing as a CMO for oral solid dosage forms (capsules and tablets). InnoGenerics received funding from Nordic governments during COVID-19 to support generic drug production.

Ion Labs, Inc.

United States

Ion Labs, Inc. is a US-based contract manufacturer of dietary supplements and nutritional products, part of HBI Health & Beauty Innovations (now Ourvita Group). With 40+ years of experience, 300+ employees, and 300,000 sq ft facilities in Largo, Florida, Ion Labs manufactures capsules, gummy vitamins, liquid capsules, cap-in-cap, powders, and tablets. The company recently completed a $30 million gummy production expansion increasing capacity to 50 million gummies per month.

Krewel Meuselbach GmbH

Germany

Krewel Meuselbach GmbH is a German owner-operated, medium-sized pharmaceutical company headquartered in Eitorf (NRW) with a production facility in Gehren, Thuringia. They are primarily a manufacturer of herbal (pflanzliche) medicines and also offer contract manufacturing (Lohnherstellung) services for third parties. Their contract services include manufacturing of liquids and tablets, packaging with serialization and aggregation capabilities, warehouse/logistics, and sales support. They produce exclusively in Germany.

LABIANA

Spain

LABIANA is a Spanish pharmaceutical group founded in 1958 with over 60 years of history, now listed on BME Growth. They operate as a CDMO serving both human and veterinary pharmaceutical sectors. LABIANA has three EU-GMP manufacturing plants: Labiana Pharmaceuticals in Corbera de Llobregat (Barcelona) for human pharma with sterile liquids, non-sterile liquids, and non-sterile solids; and Labiana Life Sciences in Terrassa (Barcelona) plus Veterinarski Zavod Subotica in Serbia for veterinary products including biologicals (viral, bacterial, and autogenous vaccines). The company is a benchmark in contract manufacturing for sterile forms and also manufactures/distributes Fosfomycin Trometamol under its own brand. Their subsidiary Zoleant Pharmaceuticals handles global marketing of niche alternative brand medicines.

Lannett CDMO

United States

Lannett CDMO is the contract development and manufacturing arm of Lannett Company, a generic pharmaceuticals company. Specializes in oral solid dose (OSD) and liquid formulations, including high-potency compounds and DEA-controlled substances. Operates a 425,000 sq ft cGMP-certified manufacturing facility in Seymour, Indiana with dedicated suites for potent drugs. Capabilities include technology transfers, modified release technology, complex formulations, and reformulation. Has over 100 product families currently in distribution. Acquired by Aurobindo Pharma USA Inc. for $250 million in July 2025. Revenue of $306 million in FY 2025.

Losan Pharma GmbH

Germany

Losan Pharma GmbH is a German full-service CDMO with 30 years of experience in the development and manufacturing of medicinal products, including solids, semi-solids, and liquids. The company's products are distributed in over 70 countries. Losan Pharma has been successfully inspected by the US FDA, ANVISA (Brazil), Saudi FDA, and Turkish authorities. The company specializes in improving API performance through enhanced bioavailability, stability, and customized release profiles.

Magle Chemoswed AB

Sweden

Magle Chemoswed AB is a Swedish CDMO serving pharmaceutical and medical device companies with comprehensive services from development through manufacturing on a contract basis. The company operates a full cGMP and ISO 13485 production site in Malmo with five dedicated manufacturing suites. Services include analytical development, process development, solid state characterization, freeze drying (lyophilization), small-scale vial fill and finish, and inhalation drug product development. FDA inspected (3 inspections: 1 NAI, 2 VAI).

Matrix Pharma Corp. Private Ltd. (CDMO BU)

India

Matrix Pharma Corp. Private Ltd. (CDMO BU) is a leading Indian integrated API manufacturer and CDMO specializing in active pharmaceutical ingredients with particular expertise in complex molecules, high-potency drugs, and APIs across therapeutic areas including antiretrovirals, antivirals, antihypertensives, cardiovascular, and CNS therapies. The company operates six state-of-the-art manufacturing facilities with over 3,850 kL installed capacity, including dedicated units for ARVs, peptides, and iron complexes. FDA-registered with 5 FEI numbers and extensive inspection history (25 inspections: 9 NAI, 15 VAI, 1 OAI). Recently inaugurated an oncology manufacturing facility in Vizag.

Medicair

Greece

Medicair is a privately-owned Greek pharmaceutical company founded in 1998, operating with vertical integration from development and manufacturing to commercialization. The company offers contract manufacturing services for solid, semi-solid, and liquid dosage forms including OTCs and food supplements. Their manufacturing specialization is in pMDI inhalers, external use sprays, foam sprays, unit dose ampoules, semi-solids, and capsules, with a production capacity of 8 million canisters. They invest over 10% of turnover in R&D and have 80+ INNs and 150+ branded generic products. Medicair also offers product development, licensing, and distribution partnerships globally.

Medisky Pharmaceuticals Pvt Ltd

India

Medisky Pharmaceuticals Pvt Ltd is a WHO-GMP certified Indian pharmaceutical company based in Ahmedabad, Gujarat, manufacturing tablets, capsules, ointments, gels, creams, lotions, and shampoos. The company provides contract manufacturing services and has manufacturing facilities with international standards. Their equipment includes rapid mixer granulators, fluid bed dryers, tablet compression machines, capsule filling machines, coating pans, tube filling machines, blister and alu-alu packing machines. They operate non-beta-lactam production lines for tablets, capsules, ointments/creams/gels, and packaging sections.

Medreich Limited

India

Medreich Limited is a fully integrated pharmaceutical company and CMO/CDMO headquartered in Bengaluru, India, with global presence including UK (Medreich PLC) and Australia. The company operates seven state-of-the-art manufacturing facilities and specializes in contract manufacturing of pharmaceutical preparations in various dosage forms for global regulated markets. Medreich offers services including proof of concept, formulation development, analytical services, clinical manufacturing, commercial manufacturing, and packaging design & development. The company has developed formulations as patent non-infringing and niche generics in differentiated dosage forms. Medreich is a subsidiary of Meiji Holdings Co., Ltd. Major clients include Sanofi, Berlin Pharma (Thailand), and others.

Meenaxy Pharma Pvt Ltd.

India

Meenaxy Pharma Pvt Ltd is an Indian pharmaceutical company with over 20 years of experience specializing in the manufacture of pharmaceutical pellets and capsules. WHO GMP and ISO 9001:2015 certified, the company is a pioneer in novel drug delivery systems, producing neutral pellets (non-pareil seeds, sugar spheres USP, tartaric acid pellets, di-calcium phosphate pellets, MCC pellets), active drug coated pellets (doxycycline, omeprazole, curcumin, orlistat, indomethacin ER, itraconazole, dexlansoprazole, ketoprofen ER, mebeverine HCl SR), enteric coated pellets, and blended pellets (iron folic, mineral & vitamin). They serve clients including GSK, Aurobindo, and Dr. Reddy's, and export to 20+ countries. The company operates two manufacturing facilities with capsule filling capabilities and contract manufacturing services.

Meribel Pharma Solutions

France

Meribel Pharma Solutions is a mid-sized European end-to-end CDMO launched with 13 sites across France, Spain, and other European locations. The company specializes in sterile multidose products, sterile and non-sterile lyophilized products, API, sachets and stick packs, along with oral solid dose, liquid and semi-solid dosage forms. Meribel provides comprehensive services from development through commercialization including regulatory affairs, analytical development, process development, tech transfer, packaging, and manufacturing.

Micro-Sphere SA

Switzerland

Micro-Sphere SA is a Swiss pharmaceutical CDMO based in Ticino, Switzerland, specializing in spray drying, capsule filling, and a wide range of R&D services. The company has a 100% regulatory track record, has served over 200 clients from all continents, and worked with over 500 drug substances and drug products. Micro-Sphere operates ISO 8 clean rooms and is FDA-registered for manufacturing. The company has a partnership with Sferalp and provides spray drying of both aqueous and organic solutions.