Find and compare companies providing Drug Product (CMO) services for:
Oral solid products
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CMO
Plants in:
Established in: 1975
Production scale:
small
medium
large
Employees: 234

45+ years of experience in oral solid and nonsterile oral liquid

Specialization in pediatric, geriatric, and controlled-substance

Reliable and flexible full-service production partner
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Plants in:
Established in: 2023
Production scale:
small
medium
large
Employees: 1000+

Expertise in Conventional, Complex, and Niche Chemistries

End-to-end Support from early development to Commercial Phases

Comprehensive Analytical Support Facilities
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CMO

Specialized in complex product development and manufacturing.

High-quality standards with a focus on customer-specific needs.

Agile and innovative approach to CDMO services.
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CMO
Plants in:
Established in: 2008
Production scale:
large
small
medium
Employees: 4.000

With 14 production sites in Europe and the USA

7 Development Centers of Excellence covering all dosage forms

13 locations with Technology Services on site for seamless Tech Transfer and product Life-Cycle Management
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Plants in:
Established in: 1886
Production scale:
medium
small
Employees: 275+

Raw materials, CMO and OTC products

Two GMP certified locations

Customisable (small-sized) packages
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CMO
Plants in:
Established in: 1964
Production scale:
small
medium
large
Employees: 135+

Market leader in Switzerland

Small and medium batch sizes

Pharmaceutical raw materials with a herbal or synthetic basis
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CMO
Plants in:
Established in: 2005
Production scale:
medium
small
Employees: 200+

Portfolio of over 2,000 APIs

Precise quality control

End-to-end global regulatory support
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Plants in:
Established in: 2016
Production scale:
small
medium
large
Employees: 200

PFAS-Free Peptides

Certified Quality & Sustainability with ISO 9000 certification and RSPO audited supplier & GMP

Specialized in APIs & Pharmaceutical Intermediates
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Plants in:
Established in: 1987
Production scale:
medium
small
large
Employees: 50+

ISO 9001:2015 & SGS audited supplier

One-stop CDMO Solutions for APl and Key intermediates

Specialized in APIs & Pharmaceutical Intermediates for 38 years
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Plants in:
Established in: 1989
Production scale:
large
Employees: 5000+

6 production facilities approved by USFDA, AGES-Austria, PMDA, WHO

R&D Centers with capabilities of ANDAs, DMFs and NDDS

462+ patents filed for drug substances and polymorphs
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CMO
Plants in:
Established in: 1972
Production scale:
medium
Employees: 1,000+

EU-GMP for APIs and CEP for certain APIs

Exporting to over 50 countries worldwide

Long-standing technological advantage in adamantane, quinuclidine and nitrofurane chemistry
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CMO
Plants in:
Established in: 1955
Production scale:
small
medium
large
Employees: 500+

BFS expertise with FDA Approval for Sterile Manufacturing

USA and European Quality

Innovative solutions for ophthalmology and otorhinolaryngology
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Plants in:
Established in: 2014
Production scale:
small
medium
large
Employees: 1000+

24 years of production experience

6 workshops and 9 production lines which has 100t/month production capacity

4 USDMFS & 8 CEPS & 200+ Patents
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CMO
Plants in:
Established in: 2006
Production scale:
small
medium
Employees: 20

Quality Assurance: Products are manufactured from the finest raw materials and undergo rigorous testing.

Tailored Customisation & Compliance: Providing end-to-end solutions to meet your business

Dependable Expertise and Supply: Backed by years of industry experience and a robust supply chain.
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CMO

Comprehensive drug development services from molecule to market.

Expertise in nanomedicine and drug repurposing.

Tailored project management ensuring efficiency and transparency.
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Replies slower than most
CMO

Advanced polymers technology for optimized drug delivery systems.

Global capabilities in complex formulations and specialty chemicals.

Emphasis on collaborative partnerships for innovative solutions.
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Replies slower than most
CMO
Plants in:
Established in: 1942
Production scale:
large

Over 100 unique marketed pharmaceutical products and 17 approved product applications since 2019

Manufacturing capacities : 3.5B Oral Solid doses and 2.0M liters of liquids per year

We specialize in contract manufacturing of Oral Solid Dose (OSD) and Liquids, including high potency substances and small molecules.
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Replies slower than most
CMO

Pioneering in advanced delivery technologies and development solutions.

Extensive global network ensuring supply chain resilience.

Tailored services across biologics, gene therapies, and pharmaceuticals.
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Replies slower than most
Plants in:
Established in: 1962
Production scale:
large

500 millions of lozenges per year at the Aignan site

143 million packs per year at the Gien site

252 formulations per year at the Cahors site
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Replies slower than most
CMO

Leaders in dermatological product development and testing.

Innovative solutions for skin permeation and absorption studies.

Strong focus on client-centric, scientifically driven services.
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Replies slower than most
CMO

Successfully inspected by TGA, PMDA, MHRA, ANVISA, Health Canada, MPA, IMB, & FDA

All facilities are in good standing with all regulatory authorities, including DEA, EPA, OSHA

Quality Management System and supporting analytical processes are almost 100% electronic
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CMO

Specialized in sterile ophthalmic and injectable formulations.

Focus on flexibility and customization for client-specific needs.

Advanced manufacturing capabilities in a controlled environment.
All certificates
Replies slower than most
Looking for Drug Product (CMO) Services?
Find a list of providers specializing in CMOs/CDMOs Services for Oral solid products. Navigate through our extensive selection to identify the supplier that aligns with your specific needs.
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Drug Product (CMO)
Drug Product CMOs (contract pharmaceutical manufacturing) specialize in formulating, manufacturing, and packaging finished dosage forms such as tablets, capsules, injectables, and liquids. These organizations enable pharmaceutical companies to bring safe, effective, and compliant medicines to market by offering GMP-certified production capabilities, scalability, and regulatory support.
Oral solid products
Oral solid outsourcing means working with a Contract Manufacturing Organization to manufacture tablets, capsules,
granules, or powders as finished dosage forms. Typical steps include blending, granulation, compression or encapsulation, coating,
in-process controls, and packaging into bottles, blisters, or stick packs.
Key constraints include content uniformity, moisture sensitivity, tooling availability, and dissolution performance. A strong oral solid CMO
also manages packaging component lead times and serialization needs for your target markets.
Use this guide to evaluate oral solid contract manufacturing services and avoid delays during tech transfer and scale-up.
Short answers to common questions about oral solid dosage form outsourcing and tablet manufacturing CMOs.
An oral solid products CMO manufactures tablets, capsules, powders, and granules as finished dosage forms. Services often include blending, granulation, compression, coating, encapsulation, and packaging. Yes. Tablet manufacturing focuses on compression tooling, hardness, friability, and coating, while capsule filling centers on fill weights and shell compatibility. A qualified CMO can offer both and advise on equipment fit. Many CMOs provide wet and dry granulation services to improve flow and content uniformity. Ask about equipment scale, binder systems, and moisture control for your formulation. Common formats include blisters, bottles, stick packs, and sachets. Packaging line compatibility and component lead times are frequent decision factors. Key tests include assay, content uniformity, dissolution, hardness, and stability. Your CMO should align methods and specifications to target markets. Some do. For high-potency APIs, confirm containment, occupational exposure limits, and cleaning validation strategies. Batch size depends on scale-up, market demand, and equipment capacity. Share your clinical or commercial forecast to confirm line fit early. It includes documentation review, trial blends or engineering batches, process validation, and stability initiation. Timelines vary with tooling and packaging readiness. Many CMOs offer packaging, but capabilities vary by line and format. Confirm serialization, labeling, and artwork management support. Common issues include blend segregation, compression scale-up surprises, and coating defects. Early process characterization and realistic timelines help reduce risk. Compare equipment capabilities, regulatory history, capacity windows, and packaging flexibility. Use this directory to shortlist CMOs by oral solid fit. Oral solid outsourcing is a subset of finished dosage form manufacturing focused on tablets and capsules. A drug product CMO can also support other dosage forms if needed. Many CMOs support stability storage and release testing, sometimes via in-house or partner labs. Clarify scope and data ownership in your RFQ. Provide formulation details, target dose, granulation method, tooling requirements, batch sizes, packaging format, and target markets. Clear inputs reduce RFQ back-and-forth.What is oral solid products outsourcing (CMO)?
When to choose a CMO for oral solid products
Common buyer requirements
Drug Product buyer guide (CMO)
How to choose the right Contract Manufacturing Organization for oral solids
RFQ template: what to include for oral solid products
Common pitfalls in oral solid contract manufacturing
Validation and regulatory notes for oral solid products
Oral Solid Products CMO services FAQ
What does an oral solid products CMO manufacture?
Is tablet manufacturing CMO support different from capsule filling?
Can a CMO help with granulation services for oral solids?
What packaging formats are common for oral solid drug product manufacturing?
Which quality tests matter most for oral solid dosage forms?
Do oral solid CMOs handle high-potency compounds?
How should I size batches for oral solid contract manufacturing?
What is the typical tech transfer workflow for oral solid products?
Do oral solid CMOs provide pharmaceutical packaging services?
What are common pitfalls in oral solid contract manufacturing?
How do I compare pharmaceutical contract manufacturing organizations for tablets?
Is finished dosage form manufacturing the same as oral solid outsourcing?
Can a pharma CMO services team support stability and release testing?
What documentation should I provide for a tablet manufacturing RFQ?























