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

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

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:

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:

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

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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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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

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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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Located in:

Germany

Plants in:

Germany

Established in: 1982

Production scale:

small

Employees: 30+

Modern GMP facility

Team of academics and technical experts

Small to large batch sizes possible

  • GMP

  • FDA

  • EMA

All certificates

  • gmp

  • fda

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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:

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:

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:

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

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

    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:

      United States

      Plants in:

      United States

      Established in: 1995

      Innovator in blow-fill-seal technology for sterile liquid dosages.

      Expertise in unit dose packaging for ophthalmics and respiratory solutions.

      State-of-the-art facilities ensuring precision and scalability.

      • GMP

      • FDA

      • EMA

      All certificates

        Replies slower than most

        Located in:

        United Kingdom

        Plants in:

        United Kingdom

        Specialized in sterile and non-sterile pharmaceutical manufacturing.

        Focus on flexibility and customization for client-specific needs.

        State-of-the-art technology ensuring quality and efficiency.

        • GMP

        • FDA

        • EMA

        All certificates

          Replies slower than most

          Looking for Drug Product (CMO) Services?

          Find a list of providers specializing in CMOs/CDMOs Services for Liquid Oral 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.

          Liquid Oral products

          What is liquid oral products outsourcing (CMO)?

          Liquid oral outsourcing is the use of a Contract Manufacturing Organization to compound, filter, fill, and package oral solutions, suspensions, or syrups. Core steps include mixing, pH adjustment, homogenization, filtration, filling, and labeling.

          Key constraints include viscosity control, sedimentation risk, microbial limits, and container compatibility. Oral liquid CMOs also manage flavor systems, preservatives, and stability programs to support supply continuity.

          When to choose a CMO for liquid oral products

          • You need scalable compounding and controlled liquid handling equipment.
          • Your formulation requires suspension stability or viscosity management.
          • You need bottle or unit-dose packaging with child-resistant components.

          Common buyer requirements

          • Target pH, viscosity range, and preservative strategy.
          • Container format, fill volume accuracy, and closure options.
          • Microbial control plan and stability protocol alignment.

          Drug Product buyer guide (CMO)

          Use this guide to evaluate oral liquid contract manufacturing services and avoid surprises in compounding and filling.

          How to choose the right Contract Manufacturing Organization for liquid oral products
          • Process capability: mixing, homogenization, filtration, and viscosity control.
          • Microbial control: clean utilities, preservative handling, and environmental monitoring.
          • Filling lines: bottle, cup, or oral syringe compatibility.
          • Stability support: real-time stability storage and testing access.
          RFQ template: what to include for liquid oral products
          • Formulation: solution, suspension, or syrup with key excipients.
          • Processing: mixing order, pH range, and filtration needs.
          • Volumes: batch size and annual demand estimate.
          • Packaging: bottle size, closure system, and labeling requirements.
          • Markets: target regions and required certifications.
          Common pitfalls in liquid oral contract manufacturing
          • Stability drift: viscosity and flavor changes over shelf life.
          • Microbial risk: insufficient preservative strategy or cleaning validation.
          • Container issues: leachables or compatibility challenges with plastics.
          Validation and regulatory notes for liquid oral products
          • Process validation: mixing and fill accuracy across batches.
          • Cleaning validation: focus on flavorings and preservatives.
          • Documentation: batch records aligned to target markets.

          Liquid Oral Products CMO services FAQ

          Answers to common questions about oral liquid contract manufacturing and liquid fill-finish.

          What does a liquid oral products CMO manufacture?

          Liquid oral CMOs manufacture solutions, suspensions, syrups, and oral drops. Services include compounding, mixing, filtration, filling, and packaging.

          What is oral suspension contract manufacturing?

          Oral suspension contract manufacturing covers controlled mixing, homogenization, and viscosity management to keep particles suspended. It also includes microbial control and stability testing.

          Do oral liquid CMOs provide bottle filling and capping?

          Most do, but line formats vary. Confirm bottle sizes, closure options, tamper evidence, and labeling requirements early.

          Can a CMO handle preservative-free oral liquids?

          Some CMOs support preservative-free oral liquids using clean processing, filtration, and packaging controls. Ask about microbial limits and shelf-life strategy.

          What quality tests are typical for oral liquid drug product manufacturing?

          Common tests include assay, pH, viscosity, microbial limits, and stability. Suspensions also require resuspendability and particle size checks.

          Is oral liquid fill finish different from solid dose packaging?

          Yes. Liquid fill finish requires controlled dosing equipment, liquid handling, and container closure integrity checks. Packaging components and compatibility are critical.

          How do I choose a syrup manufacturing CMO?

          Look for experience with viscosity control, sugar or sugar-free bases, flavoring, and microbial control. Verify line compatibility with your container format.

          What batch sizes are common for liquid oral CMOs?

          Batch sizes vary by equipment and formulation. Provide your clinical or commercial demand so the CMO can match tank and filler capacity.

          Do CMOs provide pharmaceutical packaging services for oral liquids?

          Many CMOs offer packaging including bottles, unit-dose formats, and labeling. Confirm child-resistant requirements and component sourcing responsibility.

          What are common pitfalls in oral liquid contract manufacturing?

          Pitfalls include sedimentation issues, flavor inconsistencies, and microbial excursions. Clear formulation data and stability plans reduce risk.

          How do I compare pharmaceutical contract manufacturing organizations for oral liquids?

          Compare liquid handling equipment, microbial control systems, packaging formats, and regulatory history. Use this directory to shortlist liquid oral CMOs.

          Can a pharma CMO services team support tech transfer for oral liquids?

          Yes. CMOs can support process mapping, scale-up batches, and validation runs. Share compounding parameters and critical quality attributes.

          What is finished dosage form manufacturing for oral liquids?

          It is the production of the final liquid medicine, including compounding, filling, and packaging. An oral liquid CMO focuses on manufacturing execution and supply.

          What should I include in an oral liquid RFQ?

          Include formulation type, viscosity range, target pH, batch size, container format, and target markets. These inputs help CMOs confirm line fit quickly.