Packaging & Labeling CDMOs

QuVA Pharma

United States

QuVA Pharma is a US-based FDA-registered 503B outsourcing facility specializing in sterile compounding of ready-to-administer injectable medicines for hospitals. They serve over 3,000 US hospitals and operate multiple manufacturing and forward distribution centers. They also offer AI-powered analytics (Quva BrightStream) for health-system pharmacy data insights. Notable regulatory history includes multiple OAI inspections and Class I/II recalls.

Raritan Pharmaceuticals, Inc.

United States

Raritan Pharmaceuticals is a US-based contract manufacturer specializing in OTC pharmaceuticals, consumer products, and high-end cosmetics. They develop, manufacture, and market generic OTC medicines and niche OTC brands. Their expertise includes chewable tablets, fast-dissolving tablets, powders, capsules, specialty liquids, gels, ointments, creams, and film-delivery systems. They operate from East Brunswick, NJ with FDA-registered manufacturing facilities. Notable regulatory history includes multiple recalls (15 Class II) and OAI inspection.

Recipharm AB

Sweden

Rechon Life Science AB is a subsidiary/entity within the Recipharm group, the global CDMO headquartered in Stockholm, Sweden. This entry represents the same Recipharm organization (same website: recipharm.com) with its extensive global manufacturing footprint of 15+ FDA-registered FEI numbers and 52 FDA inspections. The Perplexity research confirms Recipharm's specialization in oral solid dose, inhalation, sterile manufacturing, and HPAPI capabilities. Rechon may represent a specific Recipharm site or legacy entity. Duplicate of Recipharm AB entry -- capabilities are identical.

REMEDICA LTD

Cyprus

REMEDICA is a Cyprus-based pharmaceutical manufacturer that has been operating for over four decades, distributing products in more than 160 countries. They manufacture generics across multiple therapeutic areas and dosage forms (solid oral dose, liquids, semi-solids, sterile injectables) and offer contract manufacturing (CMO/CDMO) services. They have long-standing relationships with NGOs (UNICEF, WHO, UNRWA). They focus on B2B partnerships, own-brand commercialization (Cyprus, Eastern EU, Asia, Middle East, Africa, LATAM), and NGO supply.

Renejix Pharma Solutions

United States

Renejix Pharma Solutions (operating as HyCON Labs) is a US-based CDMO specializing in small molecule oral dosage form development and multi-modality manufacturing. The company offers end-to-end services from preformulation through commercial manufacturing, with 14+ technologies, 300+ pieces of equipment, 350+ employees, and 2+ facilities. They serve as a single-partner CDMO across all development stages.

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.

SCN BestCo

United States

SCN BestCo is a contract manufacturer of innovative pharmaceutical dosage forms for OTC drugs, vitamins, and dietary supplements. It specializes in gummy, soft chew, coated chew, and lozenge dosage forms and operates as a contract manufacturer of consumer healthcare products since 1976.

Selkirk Pharma

United States

Selkirk Pharma is a US-based sterile fill/finish contract manufacturing organization (CMO) located in Spokane, Washington. Purpose-built by fill/finish industry experts, Selkirk offers liquid-filled vial manufacturing (0.5mL to 50mL) with fully automated isolator filling, achieving >99% yield. The facility is harmonized for GMP regulatory compliance with US FDA and EU Annex 1 standards, with capacity for both clinical trials and commercial-scale production.

Serán BioScience

United States

Seran BioScience is a US-based CDMO headquartered in Bend, Oregon, recognized as a world leader in drug delivery and formulation development. The company provides comprehensive drug development and clinical/commercial manufacturing services, specializing in spray drying and particle engineering, preformulation, dosage form development, and cGMP manufacturing. Seran recently secured $200M+ from Bain Capital to build a new 100,000 sqft commercial manufacturing facility for non-sterile oral solid dose pharmaceuticals.

Sharp Sterile Manufacturing

United States

Berkshire Sterile Manufacturing (now Sharp Sterile Manufacturing, acquired by Sharp in 2023) is a specialist CDMO providing sterile injectable development and manufacturing services from its isolator-based facility in Lee, Massachusetts. All fills are 100% isolator-based using Colanar fillers, supporting clinical through small-to-mid-scale commercial production of vials, syringes, and cartridges. FDA-inspected with 8 inspections (7 NAI, 1 VAI), demonstrating strong regulatory compliance.

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.

Siegfried Group

China

Siegfried Group is a leading global CDMO with 150+ years of pharmaceutical and chemical heritage, operating 13 production sites across Switzerland, Germany, Spain, France, Malta, the USA, and China. The company provides integrated services from early-phase API development through commercial-scale drug substance and drug product manufacturing, including exclusive synthesis, generic APIs, controlled substances, HPAPI handling, sterile formulations, and viral vector manufacturing through subsidiary DINAMIQS. In January 2026, Siegfried announced acquisition of additional US-based small molecule drug substance capacity.

Singota Solutions

United States

Singota Solutions is a CDMO based in Bloomington, Indiana, focused on aseptic injectable drug development and manufacturing for pharmaceutical, animal health, and biotechnology clients. They specialize in small-batch aseptic filling using the gloveless robotic SA25 Aseptic Filling system (first commercial site in North America). Services include aseptic manufacturing of small volume parenterals (vials, syringes, cartridges), QC testing, formulation and method development, labeling and kitting, and supply chain management including GMP-compliant warehousing and cold chain storage. They recently expanded into Europe with a GDP-certified facility in Balerna, Switzerland.

SmaBio Labs

United States

SmaBio Labs is a USA-based CDMO located in Research Triangle Park, North Carolina, delivering end-to-end drug development solutions from molecule discovery to market launch. They specialize in Chemistry Manufacturing and Control (CMC) services for small molecules, peptides, biologics, and complex APIs. Their capabilities include analytical services (IND/ANDA support, method development and validation, ICH stability testing, HPLC/UPLC, LC-MS, ICP-MS, NMR, XRPD), drug discovery and process development, API manufacturing (kg-scale cGMP), product development (formulation for oral solid dose, injectables, lyophilized products), and clinical trial material manufacturing (Phase I-III). FDA registered for analytical services. They support HPAPI compounds up to OEB 5.

SMC Ltd.

Costa Rica

SMC Ltd. is a global contract manufacturer headquartered in Costa Rica with over 35 years of experience in medical device contract manufacturing and pharma services. The company offers end-to-end capabilities from device design through commercialization, including sterile fill/finish, analytical services, and drug delivery platform technologies. All facilities are FDA-registered and ISO 13485-certified.

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.

Solupharm GmbH

Germany

Solupharm Pharmazeutische Erzeugnisse GmbH is a German family-owned contract manufacturer specializing in sterile parenteral preparations in glass ampoules and glass vials since 1974. The company operates one of the most modern production facilities in Europe in Melsungen, Germany. Solupharm is FDA-registered as both an API and FDF manufacturer.

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.

Sterling Pharma Solutions

Ireland

Sterling Pharma Solutions is a global CDMO with over 50 years of experience providing API development and manufacturing services to pharmaceutical and biotech companies. The company specializes in high potency APIs, hazardous chemistry, controlled substances, peptides, flow chemistry, biocatalysis, and ADC bioconjugation across six facilities in the UK, Ireland, and US.

Sunsho Pharmaceutical Co., Ltd.

Japan

Sunsho Pharmaceutical Co., Ltd. is Japan's leading contract manufacturing pharmaceutical company, operating as a CDMO across three business verticals: health food (supplements), new applications (flavor capsules), and pharmaceuticals (generic drugs). The company specializes in capsule and formulation technologies, with the Nanryo Factory being one of the largest soft capsule manufacturing plants in Japan.

Swiss Garnier Life Sciences

India

Swiss Garnier Life Sciences is an Indian contract manufacturing organization operating multiple pharmaceutical manufacturing plants. The company produces tablets (coated and uncoated), capsules, sachets, liquids, and ointments across four manufacturing facilities. Plant 1 (Mehatpur, Himachal Pradesh) handles pharmaceutical products with 1,680 million units capacity, while Plant 2 focuses on nutraceutical and Ayush products with 2,520 million units capacity. The company achieved DIGEMID Peru certification with zero observations in September 2025.

Swiss Parenterals Limited

India

Swiss Parenterals Limited is an Indian pharmaceutical manufacturing company producing tablets, capsules, injections, and sterile eye preparations. The company has integrated with Eris Lifesciences Limited and operates as a CDMO/CMO partner. The company manufactures across a wide range of dosage forms and technologies, including parenteral drug products and oral solid dosage forms.

Synokem Pharmaceuticals Ltd

India

Synokem Pharmaceuticals Ltd is one of India's largest CDMOs, backed by TA Associates investment (2023). The company specializes in contract development and manufacturing, ethical marketing, and pharmaceutical exports. Synokem acquired Nitin Lifesciences Ltd and Parabolic Drugs Ltd to expand API production capacity. The company recently launched a modernized cephalosporin injectable manufacturing block for commercial production. Synokem's website is currently suspended but the company remains operational and expanding.

Tedor Pharma Inc

United States

Tedor Pharma is a US-based CDMO with 20+ years of experience specializing in solid oral dosage forms. Located in Cumberland, Rhode Island, they provide end-to-end outsourcing from IND/NDA/ANDA through commercial manufacture. Services include formulation development, clinical trial manufacturing (including placebo), commercial GMP manufacturing at various scales, analytical services (characterization, testing, development, QA), and clinical supply chain management. FDA-registered and inspected (5 inspections, all VAI), DEA-licensed for controlled substances Schedules II-V. They have 2 FDA-approved products (tablets, oral route). The company announced a recapitalization and new management.

Tekro Lab

Czechia

Czech pharmaceutical CRO and CDMO specializing in veterinary pharmaceuticals and animal health. Offers GMP-certified contract manufacturing of solid dosage forms (premixes, pellets, tablets) with various active substances including penicillins, tetracyclines, and potentiated sulphonamides. Also provides contract research (preclinical studies), pharmacovigilance services, and regulatory affairs for veterinary medicinal products. Over 30 years of experience in the pharma industry.

The Vanguard Utility Corporation

United States

US-based company using next-generation Blow-Fill-Seal equipment and prefabricated robotic packaging lines to fill-finish generic injectable medicines. Operational subsidiary of ApiJect. Two business approaches: (1) producing compounded pharmaceutical products for the US market through its Global Pharmacy Reserve division, and (2) licensing prefabricated fill-finish lines with their technology to pharma companies globally (Pharmaceutical Reserve Network). Focused on addressing drug shortages of generic injectables. Headquartered in Stamford, CT with operations in Newtown, PA. FDA-registered with 1 NAI inspection.

Thompson & Capper Ltd (HBI Thompson & Capper)

United Kingdom

UK-based contract manufacturer specializing in nutritional supplements and pharmaceutical tablets. Part of HBI (Healthy Business International) group, now joined Ourvita Group. Tailor-makes vitamins, minerals, health supplements, and specialty tablets. Offers a wide range of dosage formats including tablets, chewies, melts, effervescents, powders, hard gel capsules, soft gel capsules, and liquids. Handles 4,000+ raw materials. FDA-registered. Focused on nutritional and supplement contract manufacturing rather than prescription pharmaceutical manufacturing.

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.

Torbay Pharmaceuticals (Torbay Pharma)

United Kingdom

Torbay Pharma is a UK-based global CMO and licence holder specializing in contract manufacturing of terminally sterilized generic injectables. The company partners with the world's best-known pharmaceutical companies to manufacture and supply sterile injectable products to more than 20 countries. Services include sterile fill-finish (ampoules, glass/plastic vials, oral syringes), QP certification, labeling/packaging, TPN compounding, and product safety.

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.

UniD Manufacturing

Belgium

UniD Manufacturing is a Belgian CDMO fully dedicated to polymer-based long-acting formulations for sustained release and local delivery of drugs. They offer end-to-end services from proof of concept to commercialization, specializing in non-biodegradable (up to 9 years release), biodegradable (3-18 months), and resorbable (1 day to 3 months) polymer technology platforms. Applications include vaginal rings, ophthalmic implants, inserts, and other implantable dosage forms. They have 20+ years of expertise and GMP-approved cleanrooms accredited for multi-product manufacturing, with required facilities for high-potent APIs (hormones, peptides).

Valpharma Group

San Marino

Valpharma Group is a pharmaceutical and nutraceutical CDMO based in San Marino with 40+ years of experience. The group consists of Valpharma San Marino S.p.A. and Valpharma International S.p.A. (two CDMO pharmaceutical companies) plus Erba Vita Group S.p.A. (nutraceuticals). They specialize in modified-release products in capsules and tablets, including narcotic and psychotropic substances. Services include contract manufacturing, tech transfer, regulatory and e-CTD management, pharmaceutical development, stability studies, and IMP (investigational medicinal product) batch production. They operate three production plants and are routinely audited by Italian Health Authorities for GMP compliance. Products sold in 70+ countries.

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.

Vioser SA

Greece

Vioser S.A. is a Greek pharmaceutical company established in 1984 in Trikala, Greece, specializing in IV (intravenous) solution manufacturing. The company operates under GMP and offers contract manufacturing of IV solutions including custom product development. Expanding international business in Europe, Asia, and Africa. Contract manufacturing is described as a cornerstone of their strategy, with heavy investment in manufacturing facilities. Covers the full IV solution business from initial product idea to final delivery.

VUAB Pharma a.s.

Czech Republic

VUAB Pharma a.s. is a traditional Czech pharmaceutical manufacturer with over 75 years of experience, specializing in contract development and manufacturing of APIs and finished dosage forms. Part of the SAFICHEM group, the company operates multiple production centers including API manufacturing in Roztoky u Prahy, API in Brno, and biotechnology in Ceske Budejovice. VUAB is FDA-registered for API manufacturing.

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.

Wiewelhove

Germany

Wiewelhove GmbH is a German contract manufacturer specializing exclusively in solid dosage forms. The company provides galenic development, wet granulation, compaction, blending, tabletting, capsule filling, film coating, sugar coating, bottling, blistering, and packaging services. Wiewelhove positions itself as a reliable partner for all aspects of contract manufacturing of solid dosage forms.

Zile Bonbons (Zile Ltd.)

Switzerland

Zile Bonbons AG is a Swiss specialist contract manufacturer of lozenges, chews, and dragees for the pharmaceutical (OTC), nutraceutical, dietary supplement, and confectionery industries. Headquartered in Rupperswil, Switzerland, they have a dedicated OTC lozenges manufacturing plant. They provide full-service contract development and manufacturing from product conception through commercial production, including formulation development, prototyping, sourcing, manufacture, packaging, and logistics. Their technologies include stamping, cutting, moulding, and coating, with primary packaging options (wrapper/flow pack, bags, flip-top boxes, bars, blisters). They manufacture alternative drug delivery systems as centre-filled OTC lozenges with precise API dosage. They have pharmaceutical GMP expertise and are FDA-registered (FEI 3003236010) with 1 FDA inspection (VAI). Classified as CMO rather than CDMO because their development work is focused on lozenge formulation for third parties, but they do not position themselves as offering full drug development services beyond the lozenge/chew format.

ABC Farmaceutici, an ICE Pharma company, is an Italian CDMO established in 1925 specializing in oral solid and liquid formulation manufacturing. Their 76,000 sqm facility in Ivrea (near Turin) is fully GMP certified and regularly inspected by AIFA and FDA. As part of ICE Pharma, they manage the entire drug supply chain from API through finished dosage form manufacturing.

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.

Amapharm Group

Germany

Amapharm Group is a contract manufacturer specializing in gummy vitamins, jelly beans, chews, and innovative dosage forms for dietary supplements and nutraceuticals. Founded in 1977, the company pioneered the world's first vitamin gummy in 1996. They manufacture custom formulations for private label clients but do not manufacture pharmaceutical drugs.

AMW (AMW GmbH)

Germany

AMW GmbH is a specialty pharmaceutical CDMO based in Warngau, Germany, specializing in biodegradable implant formulations using hot melt extrusion technology. The company offers contract development and manufacturing of implant drug products with biotechnological active ingredients, operating under EU-GMP with capabilities spanning development, analytics, manufacturing, and regulatory affairs.

Aurena Laboratories AB

Sweden

Aurena Laboratories AB is a Swedish contract manufacturer specializing in bag-on-valve (BoV) aerosol technology for pharmaceutical and medical device applications. Based in Karlstad, Sweden, they have over 20 years of experience in clean room produced BoV aerosols, serving clients in over 50 countries. Their products include wound care sprays, ear sprays, eye wash sprays, nasal sprays, and emollient sprays. Aurena completed the transition from MDD to MDR for medical device compliance. They are primarily a medical device manufacturer rather than a pharmaceutical drug manufacturer.

Bushu Pharma is Japan's premier CDMO with over 25 years of experience, specializing in contract manufacturing of solid dosage formulations, sterile injectables, lyophilized products, and prefilled syringes for both clinical trial supplies and commercial products. The company operates five factories in Japan with GMP certifications from 56 countries including FDA, EMA, and PMDA, serving over 90 pharmaceutical companies globally with nearly 50% of sales from foreign-affiliated clients.

Caplin Point Laboratories is a fully integrated Indian pharmaceutical company with a dominant presence in Latin America and Francophone Africa, and a growing presence in the US and EU. Through its subsidiary Caplin Steriles, the company manufactures sterile injectables, ophthalmic products, pre-mix bags, and pre-filled syringes, with 46 FDA-approved products.