Drug Substance (CDMO/CRO)
Drug Product (CMO)

Find and compare companies providing Drug Product (CMO) services for:
Oral solid products

HIGHLIGHTED

Located in:

United States

Plants in:

United States

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

  • GMP

  • FDA

  • EMA

All certificates

  • fda

  • gmp

  • ema

Replies quickly

HIGHLIGHTED

Located in:

India

Plants in:

India

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

  • GMP

  • FDA

  • EMA

All certificates

  • fda

  • ema

  • gmp

Replies quickly

HIGHLIGHTED

Located in:

United States

Plants in:

GermanyFranceGreeceSwitzerlandNorwayJapan

Production scale:

large

medium

small

Specialized in complex product development and manufacturing.

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

Agile and innovative approach to CDMO services.

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

  • ema

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HIGHLIGHTED

Located in:

Germany

Plants in:

Germany

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

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

  • ema

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HIGHLIGHTED

Located in:

Germany

Plants in:

Germany

Established in: 1886

Production scale:

medium

small

Employees: 275+

Raw materials, CMO and OTC products

Two GMP certified locations

Customisable (small-sized) packages

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

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Plants in:

Switzerland

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

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

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Plants in:

United States

Established in: 2005

Production scale:

medium

small

Employees: 200+

Portfolio of over 2,000 APIs

Precise quality control

End-to-end global regulatory support

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

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Located in:

China

Plants in:

China

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

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies quickly

Plants in:

China

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

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

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Plants in:

India

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

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

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Plants in:

Latvia

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

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

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Plants in:

Spain

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

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

  • ema

Replies quickly

Plants in:

China

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

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies quickly

Located in:

United Kingdom

Plants in:

United Kingdom

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.

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies quickly

Located in:

Belgium

Plants in:

Belgium

Established in: 2018

Production scale:

large

Comprehensive drug development services from molecule to market.

Expertise in nanomedicine and drug repurposing.

Tailored project management ensuring efficiency and transparency.

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies slower than most

Located in:

United States

Plants in:

United States

Established in: 1928

Production scale:

large

Advanced polymers technology for optimized drug delivery systems.

Global capabilities in complex formulations and specialty chemicals.

Emphasis on collaborative partnerships for innovative solutions.

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

Replies slower than most

Plants in:

United States

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.

  • GMP

  • FDA

  • EMA

All certificates

    Replies slower than most

    Located in:

    United States

    Plants in:

    United States

    Established in: 1933

    Production scale:

    large

    Pioneering in advanced delivery technologies and development solutions.

    Extensive global network ensuring supply chain resilience.

    Tailored services across biologics, gene therapies, and pharmaceuticals.

    • GMP

    • FDA

    • EMA

    All certificates

    • gmp

    Replies slower than most

    Located in:

    France

    Plants in:

    France

    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

    • GMP

    • FDA

    • EMA

    All certificates

      Replies slower than most

      Located in:

      United States

      Plants in:

      United States

      Leaders in dermatological product development and testing.

      Innovative solutions for skin permeation and absorption studies.

      Strong focus on client-centric, scientifically driven services.

      • GMP

      • FDA

      • EMA

      All certificates

        Replies slower than most

        Plants in:

        United States

        Established in: 2018

        Production scale:

        large

        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

        • GMP

        • FDA

        • EMA

        All certificates

        • gmp

        Replies quickly

        Located in:

        Canada

        Plants in:

        Canada

        Established in: 2014

        Specialized in sterile ophthalmic and injectable formulations.

        Focus on flexibility and customization for client-specific needs.

        Advanced manufacturing capabilities in a controlled environment.

        • GMP

        • FDA

        • EMA

        All certificates

        • gmp

        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.

        Pharmaoffer makes it easy and convenient to send inquiries at no cost. Directly connect with your chosen supplier and take the first step towards fulfilling your pharmaceutical needs easily and efficiently.

        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

        What is oral solid products outsourcing (CMO)?

        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.

        When to choose a CMO for oral solid products

        • You have a stable formulation and need scalable tablet or capsule manufacturing.
        • You require granulation, coating, or modified-release capability.
        • You need reliable packaging execution across multiple markets.

        Common buyer requirements

        • Defined batch sizes, annual demand, and potency/containment needs.
        • Validated analytical methods and dissolution specifications.
        • Packaging formats, artwork, and serialization readiness.

        Drug Product buyer guide (CMO)

        Use this guide to evaluate oral solid contract manufacturing services and avoid delays during tech transfer and scale-up.

        How to choose the right Contract Manufacturing Organization for oral solids
        • Equipment fit: compression speed, capsule fill ranges, and coating capability.
        • Granulation options: wet, dry, or direct compression lines for your formulation.
        • Potency controls: containment and cleaning validation for high-potency compounds.
        • Packaging lines: blister, bottle, or sachet compatibility and serialization readiness.
        RFQ template: what to include for oral solid products
        • Dosage form: tablet, capsule, powder, or granule.
        • Process: granulation method, coating type, and compression parameters.
        • Batch size: clinical and commercial volumes.
        • Packaging: blister, bottle, stick pack, or sachet requirements.
        • Markets: target regions, inspections, and required certifications.
        Common pitfalls in oral solid contract manufacturing
        • Scale-up surprises: compression settings and blend flow behavior shift at scale.
        • Tooling delays: tablet tooling and change parts can add lead time.
        • Coating defects: insufficient process characterization affects appearance and dissolution.
        Validation and regulatory notes for oral solid products
        • Process validation: align protocol counts with clinical or commercial stage.
        • Cleaning validation: especially important for shared equipment and potent APIs.
        • Data integrity: confirm batch records and deviation systems meet target market expectations.

        Oral Solid Products CMO services FAQ

        Short answers to common questions about oral solid dosage form outsourcing and tablet manufacturing CMOs.

        What does an oral solid products CMO manufacture?

        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.

        Is tablet manufacturing CMO support different from capsule filling?

        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.

        Can a CMO help with granulation services for oral solids?

        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.

        What packaging formats are common for oral solid drug product manufacturing?

        Common formats include blisters, bottles, stick packs, and sachets. Packaging line compatibility and component lead times are frequent decision factors.

        Which quality tests matter most for oral solid dosage forms?

        Key tests include assay, content uniformity, dissolution, hardness, and stability. Your CMO should align methods and specifications to target markets.

        Do oral solid CMOs handle high-potency compounds?

        Some do. For high-potency APIs, confirm containment, occupational exposure limits, and cleaning validation strategies.

        How should I size batches for oral solid contract manufacturing?

        Batch size depends on scale-up, market demand, and equipment capacity. Share your clinical or commercial forecast to confirm line fit early.

        What is the typical tech transfer workflow for oral solid products?

        It includes documentation review, trial blends or engineering batches, process validation, and stability initiation. Timelines vary with tooling and packaging readiness.

        Do oral solid CMOs provide pharmaceutical packaging services?

        Many CMOs offer packaging, but capabilities vary by line and format. Confirm serialization, labeling, and artwork management support.

        What are common pitfalls in oral solid contract manufacturing?

        Common issues include blend segregation, compression scale-up surprises, and coating defects. Early process characterization and realistic timelines help reduce risk.

        How do I compare pharmaceutical contract manufacturing organizations for tablets?

        Compare equipment capabilities, regulatory history, capacity windows, and packaging flexibility. Use this directory to shortlist CMOs by oral solid fit.

        Is finished dosage form manufacturing the same as oral solid outsourcing?

        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.

        Can a pharma CMO services team support stability and release testing?

        Many CMOs support stability storage and release testing, sometimes via in-house or partner labs. Clarify scope and data ownership in your RFQ.

        What documentation should I provide for a tablet manufacturing RFQ?

        Provide formulation details, target dose, granulation method, tooling requirements, batch sizes, packaging format, and target markets. Clear inputs reduce RFQ back-and-forth.