Liquid & Semi-Solid CDMOs

Rioja Nature Pharma

Spain

Rioja Nature Pharma is a Spanish CDMO specializing in nutraceuticals and food supplements, founded in 2009 in Calahorra, La Rioja. The company manufactures softgels, capsules, tablets, powders/sachets, and liquid products under contract for third-party brands. While described as a CDMO on industry platforms, their core focus is food supplement and nutraceutical contract manufacturing rather than pharmaceutical drug manufacturing.

Rommelag CDMO GmbH (Rommelag Pharma Service)

Germany

Rommelag CDMO GmbH (Rommelag Pharma Service) is a German company that invented Blow-Fill-Seal (BFS) technology for aseptic packaging of liquid pharmaceutical products. The CDMO division provides contract filling services and product development support for liquid and semi-solid pharmaceutical products using BFS technology. Rommelag also manufactures the bottelpack BFS filling machines (up to 37,500 containers/hour) and provides comprehensive lifecycle services including qualification, validation, and factory planning.

SIDEFARMA

Portugal

SIDEFARMA is a Portuguese CMO with over 45 years of experience, specialized in the manufacture of small and medium-size batches of solid dosage forms (coated tablets, tablets, capsules), semi-solids (creams, gels, ointments), and liquid pharmaceuticals. The company provides contract manufacturing, contract packaging, and contract development services following European quality standards, while also commercializing its own branded pharmaceutical products.

Softgel Healthcare Pvt Ltd

India

Softgel Healthcare Pvt Ltd is an Indian CDMO with over 18 years of expertise in formulating, developing, and manufacturing soft gelatin capsules. Operating USFDA and EU-GMP approved facilities, the company serves over 100 partners in 60+ countries. Key products include Enzalutamide, Cyclosporine, Tafamidis, Nintedanib, and other complex softgel formulations. The company was acquired by Everstone Capital.

Special Product’s Line – CDMO Services

Italy

Special Product's Line (SPL) is an Italian CDMO founded in 1978, specializing in the production of non-sterile pharmaceutical products. The company operates a 50,000 sqm state-of-the-art facility with over 500 employees, serving more than 60 international pharmaceutical companies. SPL offers full-service CDMO capabilities from development to production and registration across a wide range of dosage forms including tablets, capsules, powders, oral liquids, creams, suppositories, ovules, and softgel capsules.

Titan Laboratories Pvt Ltd

India

Titan Laboratories Pvt Ltd is an integrated Indian pharmaceutical company and the first Indian pellet company to receive EU-GMP Written Confirmation. Established in 2004, it manufactures and exports pharmaceuticals and APIs across 47 countries, with specialization in pellets, granules, tablets, capsules, and creams/ointments. The company holds EU-GMP, TGA, ANVISA, WHO-GMP, MFDS, and other international approvals.

Tosca Pharmachem (Tosco Pharmachem Pvt Ltd)

India

Tosco Pharmachem Pvt Ltd is an Indian pharmaceutical contract manufacturing company providing third-party/contract manufacturing services for formulated pharmaceutical products. The company's website has been compromised by spam, but search results confirm it operates as a CMO offering pharmaceutical manufacturing across multiple dosage forms including tablets, capsules, liquids, and topicals.

Trident Lifeline Limited

India

Trident Lifeline Limited is an Indian pharmaceutical company established in 2014, engaged in manufacturing and marketing finished dosage forms. The company offers contract manufacturing services (hybrid model: own products + third-party manufacturing) for tablets, capsules, dry powder, liquid, ointment, gel, and injectable products. WHO-GMP compliant with global presence in 40+ countries. 3133+ products registered with India FDA, 989+ globally registered products.

Unilab Chemicals & Pharmaceuticals Pvt Ltd

India

Unilab Chemicals & Pharmaceuticals Pvt Ltd is an Indian manufacturer of Active Pharmaceutical Ingredients (APIs), bulk drugs, and finished dosage forms, established in 1978 near Mumbai. Their product portfolio focuses heavily on antiseptic and disinfectant APIs and formulations including Chlorhexidine Gluconate, Povidone Iodine, Cetrimide, Benzalkonium Chloride, and related topical/liquid formulations. They also manufacture APIs like Guaifenesin, Phenothiazine, and other pharmaceutical chemicals.

Vefa İlaç San. ve Tic. A.Ş.

Turkey

Vefa Ilac San. ve Tic. A.S. is a Turkish pharmaceutical manufacturer based in Beylikduzu, Istanbul, established in 2012 with GMP certification obtained in 2013. They manufacture pharmaceuticals, traditional herbal medicines, food supplements, and personal care products for both domestic and export markets. They have significant production capacity: 902 million tablets/year, 270 million capsules/year, 252 million coated units/year, 48 million bottles/year, and 15 million cream & gel units/year. Products are exported to Azerbaijan, Georgia, Ukraine, Iraq, Yemen, Saudi Arabia, and Romania. They hold WHO GMP and ISO 9001:2015 certifications. Their vision focuses on becoming a leading private label (contract) production base in Eurasia for pharmaceutical and nutraceutical products.

Vianex S.A.

Greece

Vianex S.A. is a prominent Greek pharmaceutical company listed on PharmaSource as a CDMO. The company is described as specializing in contract development and manufacturing. While the website content is primarily in Greek and could not be fully parsed, PharmaSource confirms CDMO services. The company appears to have multiple manufacturing facilities (Factory A, B, C, D mentioned in navigation) and covers a broad range of dosage forms. Founded by Paul J. Giannacopoulos.

West Coast Pharmaceutical Works Ltd

India

West Coast Pharmaceutical Works Ltd is an Indian manufacturer of pharmaceutical formulations primarily for human and veterinary use. The company also produces nutraceutical products. West Coast is FDA-registered and operates contract manufacturing services for pharmaceutical formulations.

Contract Packaging Resources is a member of the Aenova Group, a worldwide leading CDMO for the pharmaceutical and healthcare industry. The Aenova Group provides comprehensive pharmaceutical manufacturing including solid dosage forms, sterile fill and finish, semi-solids, non-sterile liquids, softgels, gummies, and packaging services. The Latina site in Italy serves as the central sterile manufacturing facility with capacity for over 100 million units per year, handling biologics including monoclonal antibodies, peptides, and vaccines with isolator technology.

CordenPharma is a full-service CDMO providing integrated development and manufacturing of APIs, drug products, and lipid excipients across a global network of cGMP facilities in Europe and North America. The company offers capabilities spanning peptides, oligonucleotides, highly potent and oncology compounds, small molecules, injectables, lipid nanoparticles (LNPs), and oral solid dosage forms. CordenPharma is investing over EUR 500M in a new peptide manufacturing facility in Muttenz, Switzerland, and expanding its Colorado site for large-scale peptide production.

DPT Laboratories, LTD.

United States

DPT Laboratories, Ltd., a Mylan company with over 80 years of experience, is a leading CDMO specializing in semi-solid and liquid dosage forms including creams, gels, ointments, lotions, solutions, suspensions, emulsions, and aerosol formulations. The company provides integrated services from pre-formulation through commercial-scale cGMP manufacturing and packaging.

Eromol UK Ltd (Eramol)

United Kingdom

Eramol (formerly Eromol UK Ltd) is a UK-based CDMO specializing in bespoke clinical trial manufacturing services, founded by two Qualified Persons. The company provides end-to-end services including formulation development, primary manufacturing, clinical packaging, QP release, and global distribution from MHRA and HPRA-approved facilities, with a new sterile injectable site opening in early 2026.

European Medical Contract Manufacturing (EMCM)

Netherlands

European Medical Contract Manufacturing (EMCM) is a Dutch full-service contract manufacturer and centre of excellence in developing and manufacturing sterile medicinal products for the pharmaceutical and medical device markets. The company has 2000m2 of GMP-accredited facilities with cleanrooms from class D to class A, handling liquids, suspensions, gels, and powders in ampoules, vials, pre-filled syringes, and pouches.

FAMAR

Greece

FAMAR is a leading European pharmaceutical CDMO headquartered in Greece with a network of 7 production sites and 2 R&D centers across Europe, employing approximately 1,800 people. The company provides development, manufacturing, quality, regulatory, and logistics services for a wide range of pharmaceutical and consumer care products across 80+ international markets, with capabilities spanning from oral solid dose to sterile injectables and HPAPI products.

Fareva

Brazil

Fareva is a family-owned French CDMO and the largest in France, employing 13,000 people across 41 production sites in 13 countries with EUR 2.22 billion revenue in 2025. The company provides comprehensive pharmaceutical subcontracting from API manufacturing (including HPAPIs, cytotoxics, hormones, steroids, and controlled substances) to finished drug product manufacturing and packaging across oral, sterile injectable, nasal, ophthalmic, and semi-solid dosage forms.

Fermion, a wholly owned subsidiary of Orion Corporation (Finland), is a CDMO specializing in developing, manufacturing, and marketing small molecule Active Pharmaceutical Ingredients (APIs), including HPAPIs, cytotoxics, steroids, generics, and controlled substances. Together with its parent Orion, it offers integrated contract development and manufacturing services for both drug substances and drug products, covering the full lifecycle from preclinical to commercial scale. FDA-approved since 1979 and EMA-approved since 1971.

Formulated Solutions

United States

Formulated Solutions is a U.S.-based CDMO providing formulation development, analytical development, manufacturing, regulatory affairs, and packaging services for pharmaceutical and consumer health products. The company offers flexible manufacturing from small-scale clinical batches to large-scale commercial production across multiple dosage forms.

Formulytica

Australia

Formulytica is an Australian specialty contract research, development and manufacturing organisation (CRDMO) with expertise in formulation, analytical method development, and drug product development. The company specializes in developing innovative drug formulations and analytical methods essential for clinical trial entry.

Galentic Pharma (India) Pvt Ltd

India

Galentic Pharma (India) Pvt Ltd is an Indian contract manufacturer established in 1992, specializing in sterile ophthalmic products and non-sterile dermatological products. The company operates two US FDA cGMP compliant and WHO-GMP approved manufacturing facilities with both aseptic and non-sterile capabilities. Galentic exports over 80 products to multiple countries including ophthalmic ointments/gels and a diverse range of derma topicals.

GMP Laboratories of America, Inc.

United States

GMP Laboratories of America, Inc. is a US-based CDMO providing contract development and manufacturing services for oral solid dosage forms, liquids, semi-solids, and topical products. The company offers formulation development, analytical testing, stability studies, and commercial-scale manufacturing from its FDA-registered facility. It serves pharmaceutical and dietary supplement markets.

Gofarm Sp. z o.o. Sp.k

Poland

Gofarm Sp. z o.o. Sp.k is a Polish CDMO providing contract development and manufacturing services for pharmaceutical products, dietary supplements, and cosmetics. The company offers formulation development, analytical testing, stability studies, and commercial manufacturing for oral solid dosage forms, liquids, and semi-solid products. It operates from EU GMP-compliant facilities in Poland.

Groupe PARIMA

Canada

Groupe PARIMA is a Canadian CDMO founded in 1994 specializing in the development and manufacturing of non-sterile liquids, suspensions, and semi-solid drug products. Operating from a 67,000 sq ft facility in Montreal, the company provides turnkey services from formulation development through commercial production, supplying drug products to over 30 global markets.

Groupe SYNERLAB CDMO

France

Groupe SYNERLAB (now operating as Meribel Pharma Solutions) is a mid-size European CDMO with an integrated network of manufacturing sites across Europe, providing end-to-end services from API manufacturing through finished dosage forms. The company specializes in sterile multidoses, sterile and non-sterile lyophilized products, sachets, stick packs, oral solid dose, liquids, and semi-solids.

Grünenthal PRO (Grünenthal CDMO)

Chile

Duplicate entry of Grunenthal PRO (company ID 8756785b). Grunenthal PRO is the contract manufacturing arm of Grunenthal Group, operating five specialized plants with vertically integrated manufacturing from active substance to finished products. Approximately 50% of total production is for third-party clients across 100+ countries.

Grupo Azevedos (Sofarimex)

Portugal

Grupo Azevedos, operating through its Sofarimex manufacturing unit, is a Portuguese CDMO specializing in freeze-dried injectables and sterile eye drops, with over 20 years of contract manufacturing experience. The company manufactures pharmaceutical medicines and health products for third parties across non-sterile solid, semi-solid, and liquid forms, as well as sterile products, and holds manufacturing licenses from INFARMED and multiple international authorities.

Grupo Medinfar

Portugal

Grupo Medinfar is a Portuguese pharmaceutical company founded in 1970, with an industrial unit that has provided contract manufacturing services for over 20 years. The company manufactures non-sterile solid, semi-solid, and liquid pharmaceutical products for third-party clients, offering turnkey and custom services including bulk manufacturing, packaging, analytical release, and scale-up support.

Gruppo Farma Impresa S.r.l.

Italy

Gruppo Farma Impresa is an Italian contract manufacturer specializing in medical devices based on substances, food supplements, and dermocosmetics, offering private label production (conto terzi) and out-licensing of over 1,000 ready-to-market products. The company provides formulation development, R&D with over 200 new formulations annually, regulatory affairs support, and clinical trial services across multiple therapeutic areas.

Hubot CDMO | Tri-Pac, Inc.

United States

Hubot CDMO (Tri-Pac, Inc.) is a U.S.-based contract manufacturer providing CDMO solutions for consumer healthcare (medical devices, OTC) and personal care products. The company focuses on aerosol filling, liquid filling, and proprietary dispensing solutions with an emphasis on sustainability and quality.

IDI Integratori Dietetici Italiani srl is an Italian pharmaceutical company engaged in the development and manufacturing of pharmaceutical products, dietary supplements, and medical devices. The company has FDA-registered facilities and produces a range of products including tablets, creams, oral solutions, and injectable formulations across multiple therapeutic areas.

ICE Pharma (Industria Chimica Emiliana) is an Italian integrated pharmaceutical company with over 70 years of experience and 1,500 employees worldwide. The company is a leading global producer of Ursodeoxycholic acid (UDCA) and bile acid derivatives, offering CDMO services for solid and liquid finished dosage forms and complex carbohydrates. ICE Pharma operates 7 manufacturing facilities across North and South America, Europe, Asia, and Oceania.

Jubilant HollisterStier CMO

Canada

Jubilant HollisterStier CMO (subsidiary of Jubilant Pharma) specializes in sterile fill-finish, lyophilization, injectables, ophthalmics, otics, topicals, and liquids for pharmaceutical and biopharmaceutical clients. End-to-end services from process development to inspection and packaging. Facilities in Spokane, WA and Montreal, QC. Won AWB Manufacturer of the Year 2024 and Manufacturing Excellence Award 2025. Largest manufacturer by employees in Spokane area. 92% repeat customer rate. FDA registered with 4 FEI numbers, 28 inspections (6 NAI, 18 VAI, 4 OAI -- elevated regulatory risk).

Labialfarma

Portugal

Labialfarma is a Portuguese CDMO established in 1981, specializing in the development and contract manufacturing of nutraceuticals, medicines, cosmetics, medical devices, and complementary feed products. They serve over 15 million people worldwide annually. Their capabilities span solid, semi-solid, and liquid dosage forms, with proprietary technologies including flavoring, sealed benefit protection, rapid disintegration, and SmartPACKAGING innovations. They offer end-to-end services from formulation development to finished product packaging. Labialfarma is primarily focused on the nutraceutical/food supplement space rather than prescription pharmaceuticals.

LABOMAR S.P.A.

Italy

LABOMAR S.p.A. is an Italian CDMO with 25+ years of experience, specializing in the research, development, and contract manufacturing of innovative food supplements, medical devices, foods for special medical purposes, and cosmetics. The company is a portfolio company of Charterhouse Capital Partners. LABOMAR operates as a one-stop-shop CDMO producing solid, liquid, and semi-solid dosage forms. They have expanded internationally through acquisitions including Finnish company Pharmia and Canadian company ImportFab. LABOMAR is a Certified B Corporation and primarily serves the nutraceutical rather than prescription pharmaceutical market.

Laboratorios Basi – Indústria Farmacêutica

Portugal

Laboratorios Basi - Industria Farmaceutica S.A. is a Portuguese pharmaceutical company whose mission is to develop, manufacture, market, and globally distribute medicines and therapeutic solutions built on European quality excellence with innovative technologies. They have over 240 pharmaceutical products registered across 17 therapeutic areas and are present in more than 60 countries. They operate two industrial units and offer contract manufacturing services for injectable products (small and large volume), gels, creams, ointments, syrups, oral solutions and suspensions, cutaneous solutions, and enemas. They also offer licensing, quality control, and R&D services. Their innovation arm operates through Basinnov.

Laboratorios Salvat, S.A.

Spain

Laboratorios Salvat is a Spanish pharmaceutical company with over 60 years of experience offering CDMO services. Listed on CPHI Online as a contract development and manufacturing organization, the company is recognized in the ophthalmic drugs contract manufacturing market alongside major players like Lonza and Siegfried. Their Pharmaloop facility enhances production capabilities. Primarily focused on sterile ophthalmic and otolaryngology products.

Lavipharm

Greece

Lavipharm is a dynamic, international healthcare company listed on the Athens Stock Exchange since 1995, based in Greece. Their manufacturing plant is one of the few pharmaceutical manufacturing sites in Europe with fully integrated production lines, including dedicated lines for transdermal drug delivery systems (TDDS). The production facility covers 8,000 m2 and produces tablets, capsules, transdermal systems, oral liquids, creams, and ointments under strict GMP conditions. Lavipharm collaborates with FAMAR for contract manufacturing and has launched the first locally produced medical cannabis prescription product in Greece. They also partner with other companies for manufacturing services.

Mapaex Consumer Healthcare Private Limited

India

Mapaex Consumer Healthcare Private Limited is an Indian contract manufacturer and CDMO specializing in Oral Care, Personal Care, Consumer Healthcare, and Vitamin & Mineral supplements. The company provides end-to-end services from ingredient sourcing through product development, manufacturing, packaging, compliance, and supply chain management. Mapaex also offers white label and private label manufacturing services. The company is focused on consumer healthcare products rather than prescription pharmaceuticals.

Marifarm proizvodnja in storitve d.o.o.

Slovenia

Marifarm d.o.o. is a Slovenian pharmaceutical company providing contract manufacturing services including finished dosage form manufacturing, project management, analytical services, logistics (GDP certified), herbal extract production, serialization systems, and microbiological quality control. The company is listed in pharmaceutical CMO industry databases and serves as a contract manufacturing partner for finished pharmaceutical products.

Mipharm S.p.A

Italy

Mipharm S.p.A. is a Milan-based pharmaceutical CDMO and one of the largest pharma CDMO sites in Italy. The company specializes in contract development and manufacturing of pharmaceutical products including production, packaging, R&D, and clinical trial logistics. 20% of staff is dedicated to quality. FDA-inspected (6 inspections, 1 NAI, 5 VAI).

MoNo chem-pharm Produkte GmbH

Austria

MoNo chem-pharm Produkte GmbH is an Austrian pharmaceutical contract manufacturer founded in 2000, affiliated with Sigmapharm Arzneimittel GmbH (70+ years in healthcare). The company specializes in the development and production of all types of pharmaceutical liquids — sterile and non-sterile, aqueous, oily, alcoholic, and viscous. State-of-the-art facilities for aseptic production of sterile liquids and filling into vials. Listed on CPHI for contract manufacturing, logistics/distribution, and regulatory services.

Softigel (by Procaps Group)

Brazil

Softigel, a subsidiary of Procaps Group, is a CDMO headquartered in Brazil specializing in the development and manufacturing of soft gelatin capsules (softgels). With over 4 decades of experience, 7 manufacturing plants across the Americas, and 8+ patented softgel technologies, the company has developed 500+ products and has presence in 50+ countries.

Sunny Pharmtech Inc. is a Taiwan-headquartered integrated specialty pharmaceutical CDMO specializing in high-potency APIs and drugs, including small molecules, peptides, and ADC linker-payloads. The company develops complex, high-barrier, niche drugs including ANDAs and 505(b)(2) filings, with state-of-the-art facilities offering OEB 5 containment and capabilities from early-stage formulation development to commercial manufacturing.

Swiss American CDMO is a contract development and manufacturing organization headquartered in Carrollton, Texas, specializing in topical skin care, sun care, and wound care products. The company operates a 134,200 sq. ft. cGMP facility and a second 131,070 sq. ft. facility in the Dallas Metroplex. With over 35 years of experience, they develop, manufacture, package, and commercialize topical drug, skincare, wound care, and medical device formulations.

US-based topical and transdermal pharmaceutical CDMO, now merged with MedPharm (Durham, NC). Provides end-to-end services from formulation development through commercial manufacturing for topical, transmucosal, and transdermal drug products. Specializes in semi-solids, aerosols, liquids, injections, and transdermal patches. Offers in-vitro permeation testing (IVPT), in-vitro release testing (IVRT), disease activity models, tissue protein binding, and continuous flow technologies. GMP-certified manufacturing for generics, OTC, and prescription products.