Packaging & Labeling CDMOs

Laboratorios Farmaceuticos ROVI S.A. is a major Spanish CDMO and pharmaceutical company, one of the leading European contract manufacturers for high-value-added injectable products. Their CDMO division (ROIS) operates three industrial complexes: two for injectables (Madrid and San Sebastian de los Reyes) and one for oral solid forms and packaging (Alcala de Henares). They also have two facilities in Granada for their own products (bemiparin and enoxaparin). ROVI's Madrid injectables plant is approved by EMA, FDA, and regulators in Korea, Brazil, and Gulf States, with ISO 9001, ISO 14001, and OSHAS certifications. They recently acquired a Bristol-Myers Squibb injectable drug product manufacturing site in Phoenix, Arizona for $250 million, expanding their capacity. ROVI provides end-to-end services from development to final product release, including clinical trials, stability studies, and analytical services. They have collaborated with Roche for manufacturing new medicines in development.

PiSA (Grupo PiSA / PiSA Farmaceutica) is a major Mexican pharmaceutical company manufacturing 1,500+ branded medications across 17 specialty lines in 14 production plants strategically located in Mexico. Employs approximately 30,000 workers. PiSA USA serves as the nearshore contract manufacturing arm, offering pharmaceutical and medical device CMO services. Company is a Socially Responsible Enterprise (ESR) for 15 consecutive years. Offers 'Maquila de Productos' (contract manufacturing) as a core service.

Lisapharma S.p.A. is an Italian pharmaceutical company specializing in the contract manufacturing of sterile injectable products, located in Erba (Como), Italy. The company provides sterile fill/finish services for vials, syringes, and cartridges, with capabilities in lyophilization. The website domain lisapharma.com is no longer active, but the company operates from lisapharma.it and is FDA-registered for manufacturing.

LTS Lohmann Therapie-Systeme

Germany

LTS Lohmann Therapie-Systeme AG is a leading CDMO specializing in non-invasive drug delivery systems for nearly 40 years. They are platform specialists in Transdermal Therapeutic Systems (TTS), Oral Thin Films (OTF), and Microneedle Array Patches (MAP). Their full-service CDMO offer covers the entire product lifecycle from API evaluation and feasibility through prototyping, clinical trial supply, and commercial-scale manufacturing. They have manufactured transdermal systems for nicotine, nitroglycerin, and hormone patches, as well as platforms for Parkinson's, Alzheimer's, and pain management.

mAbxience

Spain

mAbxience, a Fresenius entity, is a global CDMO with 14+ years of experience in the development and manufacture of biopharmaceuticals, specializing in biosimilars and monoclonal antibodies. They are FDA-registered with two FEI numbers for analysis and API manufacture. They have partnered with HP to develop AI solutions for optimizing monoclonal antibody and biosimilar production. Their CDMO platform offers tailored solutions with quality, agility, and flexibility in manufacturing.

Macleods Pharmaceuticals Ltd

India

Macleods Pharmaceuticals Ltd is one of India's top 10 pharmaceutical companies, operating as a CDMO for developing, manufacturing, and globally distributing pharmaceutical products. They produce diverse dosage forms including solid orals, liquid orals, topical formulations, injectables, metered dose inhalers, and dry powder inhalers across therapeutic areas including anti-TB, antimalarials, antiretrovirals, antidiabetics, antihypertensives, and antiasthmatics. They have 152 FDA-approved products, WHO prequalified medicines, and manufacturing facilities compliant with UK MHRA, US FDA, TGA, and WHO guidelines. They operate in 100+ countries.

National Resilience Inc.

Canada

Major North American biomanufacturing CDMO (branded as 'Resilience') focused on complex medicines including large molecule biologics, cell therapies, and aseptic drug product manufacturing. Operates facilities across the US and Canada. Delivers 100+ million vials and pre-filled syringes annually. Secured $825 million in financing to accelerate CDMO strategy. Offers proprietary technology platforms including Sprout Solutions, Auto-T, DAR-T (next-gen CAR-T), and Idea to Clinic services. FDA registered with 7 FEI numbers, 17 inspections.

Naveh Pharma Ltd.

Israel

Israeli pharmaceutical CDMO providing contract development and manufacturing services for solid oral dosage forms, oral liquids, and semi-solid/topical products. Offers formulation development through commercial manufacturing.

Nectar Lifesciences Ltd.

India

Indian pharmaceutical company with vertically integrated API and formulation manufacturing. FDA registered with 2 FEI numbers (operations: ANALYSIS, API, FDF). Offers CDMO services alongside own branded products. Manufactures both APIs (including beta-lactam antibiotics) and finished dosage forms across oral solids, injectables, and lyophilized products.

NovaCina is a sterile injectable CDMO based in Perth, Western Australia, launched by Bridgewest Group. The company manufactures sterile injectable drug products for all phases from development through commercial production. NovaCina has expanded its facility with a high-tech SA25 GMP filling line for small-batch sizes and has since merged with BioCina to create an end-to-end CDMO offering integrated biopharmaceutical and small molecule contract manufacturing services.

OLIC (Thailand) Limited is one of the largest toll and contract manufacturers in Southeast Asia for branded pharmaceutical and healthcare products. The company is a subsidiary of Fuji Pharma and serves over 30 multinational companies including most Big Pharma organizations. OLIC's PIC/S-compliant manufacturing facility produces a wide range of dosage forms including sterile liquids, oral solids, semi-solids, and liquids, serving markets in Thailand, Southeast Asia, Japan, Australia, the US, and Europe.

Olive HealthCare is a fully-integrated Indian pharmaceutical company specializing in the development, manufacturing, and marketing of soft gelatin capsule formulations for pharmaceutical, OTC, and dietary supplement products. Operating three state-of-the-art manufacturing units in India, the company provides CDMO services including toll manufacturing and full development for global partners.

Oman Pharmaceutical Products Co. LLC is a pharmaceutical manufacturer based in Salalah, Oman, engaged in inhouse formulation manufacturing, out-licensing, and CDMO business. The company produces oral solid dosage forms including tablets and offers contract manufacturing services to partners in the region and beyond.

PHIL Inter Pharma is a CMO/CDMO operating two manufacturing sites in the same industrial park in Vietnam. The company is a soft capsule manufacturer offering CMO/CDMO services from a UK MHRA GMP-accredited facility for pharmaceuticals. PHIL Inter Pharma has 250-499 employees and also manufactures generics/biosimilars. Products include the KOSENA and CALEDO brands. The company has South Korean origins (KR) and a US presence (PHIL Inter Pharma USA). No website data was available for detailed analysis.

Pii (Pharmaceutics International, Inc.), acquired by Jabil in February 2025, is a US-based CDMO specializing in complex formulations. With over 30 years of experience and 300+ scientists and support staff, Pii handles potent compounds, complex formulations, aseptic injectables, complex oral dosage forms, and high-potency soft gels. Offers phase-appropriate support from early development through commercial manufacturing. Located in Hunt Valley, Maryland. 100% FDA licensed with 5 drug product approvals in 2023.

Reig Jofre (Laboratorio Reig Jofre, S.A.) is a Spanish pharmaceutical company founded in 1929 that operates both as a pharmaceutical company with its own products and as a CDMO. They have four development and production centres in Europe (two in Toledo, one in Barcelona, one in Sweden) with over 1,100 employees. Their CDMO capabilities include sterile lyophilizates, sterile liquids, non-sterile liquids, and beta-lactam manufacturing. Known for excellence in freeze-drying technology and advanced sterile manufacturing. FDA-registered with manufacturing and analysis operations, though regulatory history shows 3 OAI inspections.

Ropack Pharma Solutions is a privately held CMO/CDMO based in Montreal, Canada, specializing in solid oral dose contract manufacturing and comprehensive packaging services. With nearly 50 years of experience, the company provides drug development, tech transfer, clinical and commercial manufacturing, and serialized packaging services for solid oral dosage forms.

Savi Pharmaceutical Joint Stock Company (Savipharm J.S.C, SVP) is a Vietnamese pharmaceutical company founded in 2005 in Ho Chi Minh City. The company operates an oral solid dose factory and provides contract manufacturing of dosage form drugs, franchising, and technology transfer services.

Shree Venkatesh International Limited (SVIL) is an Indian manufacturer and exporter of male and female human hormonal products, including both APIs and finished dosage forms. The company offers contract manufacturing services for pharmaceutical drug products and APIs, with a focus on hormonal therapies. SVIL markets its products internationally through branded and generic channels.

Sovereign Pharmaceuticals, LLC is a U.S.-based CDMO located in Fort Worth, Texas, specializing in small-batch prescription drugs. The company packages both solid and liquid pharmaceutical products and has a high potency pharma suite. Sovereign has over 30 years of expertise and was acquired through bankruptcy proceedings by Alora Pharmaceuticals.

Tirupati Group is one of India's largest contract development and manufacturing organizations (CDMOs), providing end-to-end solutions across pharmaceuticals, nutraceuticals, Ayurveda, and sports nutrition. Founded in 2005, the company operates state-of-the-art manufacturing facilities in Paonta Sahib (Himachal Pradesh) and Noida (Uttar Pradesh), serving 350+ clients including Abbott, Pfizer, Dr. Reddy's, and Sun Pharma.

Topa Thermal

Netherlands

Topa Thermal is a Netherlands-based global leader in thermal packaging systems for temperature-controlled pharmaceutical logistics. With over a century of packaging expertise, the company designs and supplies advanced thermal solutions to ensure safe temperature-controlled distribution of pharmaceutical products. It is a thermal packaging supplier, not a drug manufacturer.

E-Pharma Trento S.p.A. is an Italian CDMO specialized in solid oral dosage forms, offering a high level of outsourcing from drug development to private label manufacturing. The company is known for its sublingual technology and serves pharmaceutical companies with contract development and manufacturing services.

Flagship Biotech International is an Indian pharmaceutical company headquartered in Mumbai with manufacturing facilities across India (Tarapur, Navsari, Naroda, Baddi). It manufactures a broad range of pharmaceutical dosage forms including tablets, capsules, injectables, LVP, SVP, inhalers, ointments, and suppositories for its own brands and contract manufacturing for organizations globally in 45+ countries.

Genuone Sciences Inc. is a South Korean pharmaceutical CDMO valued at approximately $752 million, offering specialized contract development and manufacturing services including formulation development through finished product production. The company provides pharmaceutical manufacturing and analytical services for both domestic and international clients. Genuone is 100% owned by IMM Private Equity.

Glatt Pharmaceutical Services is a CDMO division of the Glatt Group that supports pharmaceutical and biotech companies from initial formulation design to commercial-scale manufacturing. The company specializes in oral solid dosage forms using advanced technologies including fluidized bed systems, spray granulation, Wurster coating, hot-melt extrusion, and amorphous solid dispersions for solubility enhancement and modified release.

LubecaFill

Germany

LubecaFill is a German contract filling company offering sterile filling services for liquid dosage forms using Ready-to-Fill (RTF) technology. They provide filling into pre-sterilized vials, syringes, and cartridges, as well as contract filling of ampoules, oral and topical liquid dosage forms, and diagnostics/laboratory consumables. GMP certification is in preparation.

Luye Pharma (EU CDMO)

China

Luye Pharma's EU CDMO operation is based in Germany and is among the largest and most respected European manufacturing sites for Matrix Transdermal Therapeutic Systems (TDS). They offer one-stop-shop CDMO services for transdermal patches covering feasibility, formulation, upscaling, clinical trial material supply, analytical services, blending & coating, cutting/packaging, and full-scale manufacturing. They have a dedicated facility for hormone-containing patches and are fully compliant for handling controlled substances.

Lyomark Pharma GmbH

Germany

Lyomark Pharma GmbH is a German CDMO specializing in sterile medicinal products. They organize contract manufacturing based on dossiers they compile and maintain, and offer regulatory services. Through their subsidiary Lyocontract, they operate a state-of-the-art pharmaceutical manufacturing site. They have 39 FDA-approved products across injectable, oral solid, and liquid dosage forms. The company focuses on niche indications for the hospital market with global distribution.

Morgen Pharmaceutical Services (MPhS), operating as Stason Pharmaceuticals, is a US-based CDMO offering end-to-end drug development and manufacturing services. Located in Irvine, California, the facility can produce over 2 billion oral doses per year with batch sizes from 0.5 kg to 600 kg. The company offers API synthesis (through offshore affiliates), formulation development, pre-formulation studies, solid dosage manufacturing (tablets and capsules), high-containment operations for highly potent compounds (OEL < 1 µg/m³), and injectable/liquid manufacturing through a partner facility in Tainan, Taiwan. FDA-registered with 2 FEI numbers and 11 FDA inspections (8 NAI, 3 VAI).

Indian pharmaceutical CDMO specializing in pre-finished formulation intermediates (PFI) and finished dosage forms (FDF). Manufactures oral solids, oral liquids, injectables, ophthalmics, topicals, and inhalation products. Strong focus on pellet technology and nanotechnology-based drug delivery systems. CRAMS (Contract Research and Manufacturing Services) provider.

Nanjing Sino Pharmaceutical Ltd.

China

Chinese pharmaceutical company specializing in production, R&D, and export of generic medicines globally. Covers 1,000+ products across antibiotic, antimalarial, analgesic-antipyretic, cardiovascular, respiratory, antiviral/anti-cancer, hormone, and other therapeutic categories. 20+ years of international registration and export experience in dozens of countries. FDA registered with 3 FEI numbers.

NEON LABORATORIES LTD

India

Indian pharmaceutical company (established 1984) that emerged as a leader in anesthesia and critical care products. Manufactures 500+ products sold in 70+ markets. Multi-located manufacturing facilities including API and formulations. Started as contract manufacturer for anesthesia products (1992) and grew into branded generics. Major plant at Palghar with 460 million units capacity. Has dedicated manufacturing units for cephalosporins and oncology to avoid cross-contamination. 2000+ employees. FDA registered with 3 FEI numbers, 29 inspections (13 NAI, 15 VAI, 1 OAI). Began API production in 2008. Also has medical devices division (HOSPRO).

Pharmatis is a leading European CDMO specializing in liquid and gel pharmaceutical forms packed in sachets, stick-packs, and bottles. The company manufactures pharmaceutical products in liquid forms including aqueous and hydro-alcoholic solutions, suspensions, and syrups. Based in France, Pharmatis is described as the world leader in pharmaceutical sachet packaging. Note: the pharmatis.com domain is currently for sale; the company appears to operate via pharmatis.fr. The website data available was only the domain-for-sale page, so classification is based primarily on search results and CPHI listings.

Eubioco is a Polish contract development and manufacturing organization (CDMO) offering contract manufacturing of medicines, supplements, and veterinary products. The company has an office and production complex in Dywity and employs more than 150 people, with capabilities spanning pharmaceutical and nutraceutical liquid and semi-solid forms.

Fischer Soehne AG is a Swiss company specializing in life science packaging solutions, including injection-moulded parts, printed containers, tubs, and nests for pharmaceutical products. It provides R&D and contract manufacturing of packaging components, not pharmaceutical drug products.

FRIKE Pharma AG is a Swiss pharmaceutical contract manufacturer (CMO) providing GMP-compliant contract manufacturing, filling, and packaging services for pharmaceutical products. The company specializes in liquid, semi-solid, and solid dosage forms including pump sprays, suppositories, lotions, ointments, and tinctures.

Hubert De Backer nv is a Belgian company specializing in the manufacture of intramammary and paste syringes and pharmaceutical packaging materials. The company provides packaging solutions and medical devices for the pharmaceutical industry.

Klass Pack Limited (now a subsidiary of Borosil Scientific Limited) is an Indian manufacturer of primary pharmaceutical glass packaging, specifically tubular glass vials. Borosil acquired a majority stake to enter the primary pharma glass packaging business. Klass Pack manufactures borosilicate glass vials for pharmaceutical use and has been expanding production capacity. They are a primary packaging component supplier, not a contract drug manufacturer.

Lucent Biotech Limited

India

Lucent Biotech Limited is an Indian third-party pharmaceutical manufacturer founded in 2006 in Roorkee (Haridwar). They manufacture a wide spectrum of pharmaceutical formulations and serve as suppliers for multiple Indian and multinational pharmaceutical companies. They are a contract manufacturer (third-party manufacturer) of pharmaceutical finished dosage forms.

Lyophilization Technology, Inc. (LTI)

United States

Lyophilization Technology, Inc. (LTI) is a US-based CDMO focused on lyophilization (freeze-drying) development and sterile clinical supply manufacturing. They offer development sciences (formulation development, thermal analysis, cycle design, product characterization, pilot plant scale-up), clinical manufacturing (Phase I, II, and toxicology), and technical services. They have specialized capabilities in dual chamber cartridges and syringes, and isolation/containment for potent compounds.