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    Pharma Services Category of Eurofins CDMO

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    HTL Biotechnology is the world leader in the responsible development and production of pharmaceutical-grade biopolymers.
    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
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    01 API Development (12)

    02 Active Pharmaceutical Ingredients (1)

    03 Analytical Method Development (1)

    04 BioAnalytical Services (1)

    05 Biologic Drugs (2)

    06 Biologics, Bioprocess & Fermentation (1)

    07 Capsule (3)

    08 Clinical Services (5)

    09 Clinical Supply (1)

    10 Contract Services (5)

    11 Cream / Lotion / Ointment (1)

    12 Cytotoxic Compound (1)

    13 Emulsion (1)

    14 Formulation Development (16)

    15 Gel (1)

    16 High Potency APIs (HPAPIs) (1)

    17 Injectable / Parenteral (3)

    18 Liquid (2)

    19 Lyophilization (1)

    20 Packaging & Logistics (3)

    21 Powder (2)

    22 Preformulation & Material Science (9)

    23 Protein / Peptide (1)

    24 Regulatory Affairs / Pharmacovigilance (2)

    25 Scale Up (1)

    26 Small Molecules (1)

    27 Solution (1)

    28 Stability Studies (2)

    29 Suspension (1)

    30 Tablet (3)

    31 Technologies (2)

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    01 Eurofins CDMO (87)

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    01 France (87)

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    Eurofins CDMO

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    DMPK

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    Eurofins Contract Development & Manufacturing Organization is the leading partner for specialized preclinical services for a complete IND/IMPD package that includes Drug Metabolism and Pharmacokinetic (DMPK) studies.

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    Pharma Service: API & Drug Product Development

    Category: Preformulation & Material Science

    Sub Category: PK / PD / TK
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    API DEVELOPMENT & CONTRACT MANUFACTURING

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    Eurofins CDMO provides API technology development services for the scale-up of complex small molecules with biotechnology and pharmaceutical applications including more potent APIs (HPAPIs) and cytotoxic compounds.

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Overview
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    API DEVELOPMENT & VALIDATION

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    Eurofins CDMO is experienced with the development & validation of several molecule API processes that are in various stages of regulatory approval across the globe. Their cGMP units are equipped with cryogenic, hydrogenation & chromatography capabilities.

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Overview
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    API COMMERCIALIZATION SUPPORT

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    Combining process chemistry expertise with analytical solutions, Eurofins CDMO provides Active Pharmaceutical Ingredient (API) development services, route scouting & commercialization support to pharma companies.

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    Pharma Service: Sales, Marketing, Registration

    Category: Active Pharmaceutical Ingredients

    Sub Category: France
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    SOLID STATE

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    Through the integration of synthetic process R&D, solid state R&D, preformulation and formulation development, Eurofins CDMo offers a knowledge-based quality-by-design approach throughout the API development and manufacturing.

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    Pharma Service: API & Drug Product Development

    Category: Preformulation & Material Science

    Sub Category: Solid State Characterization
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    FATE & PURGE SERVICES

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    Eurofins CDMO has strong experience in impurity control strategy from IND through to commercial stages and have demonstrated track-record in the design and execution of fate and purge studies.

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Overview
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    IMPURITY SYNTHESIS

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    Eurofins CDMO identifies, isolates & synthesizes process related impurities to support process development, analytical control & regulatory requirements. They offer services for the whole drug development process & manage impurities synthesis & control.

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Impurity / Reference Standard
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    PROCESS DEVELOPMENT & OPTIMIZATION

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    Eurofins CDMO has a high degree of expertise process development, successfully introducing hundreds of chemical steps to cGMP scale up and advancing several APIs from route scouting through to commercialization.

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    Pharma Service: API & Drug Product Development

    Category: Formulation Development

    Sub Category: Process Development & Optimization
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    API DEVELOPMENT PROCESS OPTIMIZATION

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    Eurofins CDMO team has considerable experience with process development, cGMP scale up & advancing several API’s to commercialization. It performs different CDMO services such as process optimization, analytical method development, stability studies, etc.

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Process Development & Optimization
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    PRE-FORMULATION / FORMULATION

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    Early formulation development compliments Eurofins CDMO's IND enabling services through a targeted formulation design. Their scientists use strategies and technologies focused on bioavailability and steered by client's objective.

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    Pharma Service: API & Drug Product Development

    Category: Preformulation & Material Science

    Sub Category: Overview
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    DRUG PRODUCT DEVELOPMENT OF SMALL MOLECULES

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    Eurofins provides integrated, end-to-end CDMO development and manufacturing services for drug substance/API and drug product manufacturing for biologics and small molecules.

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    Pharma Service: API & Drug Product Development

    Category: Formulation Development

    Sub Category: Overview
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    HPAPIs / CYTOTOXICS TABLET MANUFACTURING

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    Eurofins CDMO's state-of-the-art dedicated cGMP facilities are equipped and contained to offer diverse range of High Potency API development manufacturing solutions both in early as well as late stage development programs.

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    Pharma Service: Drug Product Manufacturing

    Category: Tablet

    Sub Category: High Potency APIs (HPAPIs)
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    HIGHLY POTENT APIs CAPSULE

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    Eurofins CDMO offers integrated product development services through the entire drug product life cycle, from highly potent active pharmaceutical ingredients (HPAPIs) forward.

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    Pharma Service: Drug Product Manufacturing

    Category: Capsule

    Sub Category: High Potency APIs (HPAPIs)
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    HPAPI / CYTOTOXICS INJECTABLE MANUFACTURING

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    Eurofins CDMO offers integrated development services through the entire drug product life cycle, from highly potent active pharmaceutical ingredients (HPAPI) forward.

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    Pharma Service: Drug Product Manufacturing

    Category: Injectable / Parenteral

    Sub Category: High Potency APIs (HPAPIs)
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    CELL BANKS

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    Eurofins CDMO offers expert capabilities for the development, preparation & characterization of a variety of microbial, mammalian & insect cell banks. They offer complete portfolio of cell banking services, with the manufacture of cell banks under cGMP.

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    Pharma Service: API & Drug Product Development

    Category: Formulation Development

    Sub Category: Overview
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    BIOLOGICAL DRUG PRODUCT MANUFACTURING

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    Eurofins CDMO delivers solutions to its customers for the development and biomanufacturing of a broad range of biological molecules and product types (antibodies, proteins, enzymes, vaccines. etc.)

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    Pharma Service: Drug Product Manufacturing

    Category: Biologic Drugs

    Sub Category: Overview
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    BIOLOGICS PRE-FORMULATION / FORMULATION

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    During the pre-formulation phase, Eurofins CDMO determines the physical & chemical properties of the API. Their team has experience with a wide range of different drug delivery routes, drug delivery systems and drug production technologies.

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    Pharma Service: API & Drug Product Development

    Category: Preformulation & Material Science

    Sub Category: Overview
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    HPAPI / CYTOTOXICS - BIOLOGICS MANUFACTURING

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    Eurofins CDMO offers integrated development services through the entire drug product life cycle, from highly potent active pharmaceutical ingredients (HPAPI) forward.

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    Pharma Service: Drug Product Manufacturing

    Category: Biologic Drugs

    Sub Category: High Potent
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    LYOPHILIZATION / FREEZE DRYING CYCLE

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    Eurofins CDMO can to help you in formulation transition from liquid to freeze dry form, solubilization & formulation study for injection, freeze drying cycle development & optimization.

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    Pharma Service: API & Drug Product Development

    Category: Formulation Development

    Sub Category: Lyophilization
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    INJECTABLE - EMULSION MANUFACTURING

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    The Eurofins CDMO teams are highly experienced in the development of all galenic form. Powder or liquid, using water, non-aqueous phases and available solvants for sterile administration.

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    Pharma Service: Drug Product Manufacturing

    Category: Emulsion

    Sub Category: Injectable
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    INJECTABLE SOLUTION MANUFACTURING

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    The Eurofins CDMO teams are highly experienced in the development of all galenic form. Powder or liquid, using water, non-aqueous phases and available solvents for sterile administration.

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    Pharma Service: Drug Product Manufacturing

    Category: Solution

    Sub Category: Injectable
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    INJECTABLE - SUSPENSION MANUFACTURING

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    The Eurofins CDMO teams are highly experienced in the development of all galenic forms including powder or liquid for sterile administration. They have expertise for various formulations such as sterile powders, suspensions, sterile semi-solids, etc.

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    Pharma Service: Drug Product Manufacturing

    Category: Suspension

    Sub Category: Injectable
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    POWDER

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    All types of APIs can be manufactured in Eurofin's facilities where they develop specific expertise for the fill & finish of other liquid formulations than standard ones such as sterile powders, suspensions, sterile semi-solids, etc.

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    Pharma Service: Drug Product Manufacturing

    Category: Powder

    Sub Category: Injectable
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    LIQUIDS

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    Eurofins offers drug product development contract services encompassing preclinical development, formulation screening and development of liquid dosage forms for nasal, parenteral, ophthalmic and oral drug delivery.

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    Pharma Service: Drug Product Manufacturing

    Category: Liquid

    Sub Category: Overview
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    SEMI-SOLIDS

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    Eurofins CDMO offers drug development contract services encompassing preclinical development, formulation screening and development, analytical development of semi-solid dosage forms for skin, mucosal or oral delivery.

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    Pharma Service: Drug Product Manufacturing

    Category: Cream / Lotion / Ointment

    Sub Category: Overview
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    SOLIDS - POWDER MANUFACTURING

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    All type of APIs can be manufactured in Eurofins facilities where they develope specific expertise for the fill & finish of other liquid formulations than standard ones such as sterile powders, suspensions, sterile semi-solids etc.

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    Pharma Service: Drug Product Manufacturing

    Category: Powder

    Sub Category: Overview
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    SOLIDS - TABLET MANUFACTURING

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    Eurofins offer a full suite of drug development services encompassing preclinical development, formulation screening and development, analytical development of solid dosage forms for oral delivery.

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    Pharma Service: Drug Product Manufacturing

    Category: Tablet

    Sub Category: Overview
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    SOLIDS - CAPSULE MANUFACTURING

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    Eurofins CDMO offers a full suite of drug product development services encompassing preclinical development, formulation screening & development, analytical development of solid dosage forms for oral delivery, etc.

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    Pharma Service: Drug Product Manufacturing

    Category: Capsule

    Sub Category: Overview
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    PRIMARY PACKAGING

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    Eurofins CDMO can provide primary packaging services for non-sterile solid forms (capsules & tablets) in HDPE bottles or blister packagings in class C rooms. They provide a large range of bottles from 15 to 600 mL with several options for caps.

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    Pharma Service: Packaging

    Category: Clinical Services

    Sub Category: Overview
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    SECONDARY PACKAGING

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    Eurofins CDMO can perform customized labeling and secondary packaging at every clinical trial phase for sterile and non-sterile dosage forms (blisters, blister-cards, vials, syringes, bottles).

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    Pharma Service: Packaging

    Category: Clinical Services

    Sub Category: Secondary Packaging
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    CLINICAL TRIAL PACKAGING & LABELING

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    Eurofins CDMO can perform customized labeling and secondary packaging at every clinical trial phase for sterile and non-sterile dosage forms (blisters, blister-cards, vials, syringes, bottles).

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    Pharma Service: Packaging

    Category: Clinical Services

    Sub Category: Label
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    QP SERVICES FOR CLINICAL SUPPLIES

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    Eurofins CDMO provides QP services including all the quality and regulatory support for clinical trial supplies. They can also provide GMP certification, documentation review, audits of manufacturing sites, QP agreement, and final batch release.

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    Pharma Service: Packaging

    Category: Clinical Services

    Sub Category: Overview
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    GMP STORAGE & DISTRIBUTION

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    Eurofins CDMO (Contract Development & Manufacturing Organization) offers GMP storage of 560 m3 at 15-25°C, 146 m3 at 2-8°C, 2.6 m3 at 20°C and 0.5 m3 at -80°C.

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    Category: Clinical Services

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    IND / IMPD SERVICES

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    Eurofins CDMO offers the skills & capability to prepare & review documents for clinical trial application (IND/IMPD). This includes manufacture & support for Phase I, II & III studies, IND/IMPD quality sections related to drug substance & drug product.

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    Pharma Service: Sales, Marketing, Registration

    Category: Regulatory Affairs / Pharmacovigilance

    Sub Category: France
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    NDA / CTD SERVICES

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    Eurofins CDMO regulatory experts will draft, review and manage the necessary documents to enable the building of Common Technical Document (CTD) for product registration and life-cycle submissions.

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    DRUG PRODUCT DEVELOPMENT - BIOLOGICS

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    Eurofins provides integrated, end-to-end CDMO development and manufacturing services for drug substance/API and drug product manufacturing for biologics and small molecules.

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    STABILITY STUDIES

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    Eurofins performs ICH compliant stability studies including stress studies, accelerated and long-term stability studies to support regulatory CMC programs and process development.

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    PHOTOSTABILITY STUDIES

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    Eurofins offers ICH photostability testing capability including stability studies including stress studies, accelerated and long-term stability studies to support regulatory CMC programs and process development.

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    PARTICLE SIZE REDUCTION & MICRONIZATION

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    To support API solid form R&D programs, Eurofins CDMO applies particle-size reduction and screening technology for discovery of new polymorphs or automated crystallization scale-up development.

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    BIOANALYTICAL SERVICES

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    Eurofins CDMO, a leading partner for specialized preclinical services offers a complete IND/IMPD package that includes ADME/DMPK, genotoxicity studies, safety pharmacology, safety assessment/toxicology, bioanalytical support (small & large molecule).

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    IMPURITIES ISOLATION & IDENTIFICATION

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    Eurofins CDMO offers a complete CMC gap analysis & risk assessment including fate & purge studies & impurities markers synthesis. They offer chromatography for the isolation of process impurities, LC/MS-MS/MS and multi-nuclear NMR for characterization.

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    Category: Analytical Method Development

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    cGMP SCALE-UP CAPABILITIES

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    Eurofins CDMO's cGMP scale-up facility can handle potent compounds to less than 30 ng/m (Safebridge™ Class 4) offering chemical steps to cGMP scale up and thus advancing several API’s to commercialization with their broad range of experience & knowledge.

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    API ROUTE DESIGN & SCOUTING SERVICES

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    Eurofins Contract Development & Manufacturing (CDMO) offers integrated development services including synthetic route design and route scouting through their process research & development (PR&D) expertise on scale-up synthesis of APIs.

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    INTERMEDIATES DEVELOPMENT

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    Eurofins CDMO offers process research & development (PR&D) expertise in R&D synthesis of starting materials, intermediates, impurities and reference standards, scale-up of APIs including synthetic route design / route scouting, etc.

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    DEVELOPMENT OF HPAPIs

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    Eurofins CDMO offers integrated development services through the entire drug product life cycle for highly potent active pharmaceutical ingredients (HPAPIs). Their R&D and analytical facilities are equipped to handle HPAPIs up to SafeBridge Class IV.

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    BUCCAL DELIVERY

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    Eurofins CDMO, with its expertise in small and large molecules, provides drug product development services for various oral liquid and solid dosage forms such as buccal drug delivery systems, parenteral formulations, ophthalmics, topical products, etc.

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    FORMULATION DEVELOPMENT FOR CAPSULES

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    Eurofins CDMO provides formulation development services for a wide range of drug delivery routes, drug delivery systems including liquid & solid oral forms (capsules, tablets), parenteral formulations, ophthalmics, topicals, etc.

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    IMMEDIATE & CONTROLLED RELEASE DOSAGE FORMS

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    Eurofins CMDO offers a wide range of drug product development and manufacturing technologies for immediate and controlled release with liquid, solid and semi-solid dosage forms for oral, nasal, buccal and topical delivery.

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    EMULSION FORMULATION DEVELOPMENT

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    Eurofins CDMO's newly commissioned HPAPI GMP suites in Ghent (Belgium), has state-of-the-art facilities for the development of emulsions, solutions, micro- and nanosuspensions of highly potent API's up to OEB5 level for early phase clinical studies.

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    FORMULATION DEVELOPMENT FOR NASAL DELIVERY

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    Eurofins CDMO provides formulation development services for a wide range of drug delivery routes, drug delivery systems including nasal & intranasal delivery, pulmonary delivery, parenteral formulations, ophthalmics, topicals, buccal delivery, etc.

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    PARENTERAL FORMULATION DEVELOPMENT

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    Eurofins CDMO provides formulation development services for a wide range drug delivery routes and drug delivery systems such as parenteral formulations, nasal and intranasal delivery, pulmonary delivery, ophthalmics, topicals, buccal delivery, etc.

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    Sub Category: Injectable / Parenteral
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    LIQUID FORMULATION DEVELOPMENT

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    Eurofins CDMO provides formulation development services for a wide range of drug delivery systems including liquid formulations such as parenteral formulations, ophthalmics, topicals, nasal, intranasal delivery, pulmonary delivery, etc.

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    OPHTHALMIC FORMULATION DEVELOPMENT

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    Eurofins CDMO provides formulation development services for a wide range of drug delivery routes, drug delivery systems including ophthalmics, oral liquid & solid formulations, parenteral formulations, topicals, buccal delivery, pulmonary delivery, etc.

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    MICRO & NANO SUSPENSIONS DEVELOPMENT

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    Eurofins CDMO's newly commissioned HPAPI GMP suites in Ghent (Belgium), has state-of-the-art facilities for the development of micro- and nanosuspensions, solutions, emulsions of highly potent API's up to OEB5 level for early phase clinical studies.

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    Sub Category: Suspension
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    FORMULATION DEVELOPMENT OF TABLETS

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    Eurofins CDMO offers strong experience in a wide range of different drug delivery routes, drug delivery systems and drug production technologies, including oral & solid formulations (tablets, capsules), buccal delivery, etc.

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    TOPICAL FORMULATION DEVELOPMENT

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    Eurofins CDMO provides formulation development services for a wide range of different drug delivery routes, including topicals such as gel, cream, lotion, ointment, parenteral formulations, ophthalmics, buccal delivery, nasal, intranasal delivery, etc.

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    CHIRAL RESOLUTION

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    Eurofins CDMO, offers diastereomeric crystallization, a chiral resolution technique based on differences that diastereomers or diastereomeric salts of enantiomers exhibit in their physicochemical properties such as different solubility.

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    Sub Category: Chiral Resolution Screening
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    POLYMORPH SCREENING

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    Eurofins CDMO offers polymorph screening contract services by investigating isolation and crystallization of the API to identify and characterize new solid forms (polymorph, hydrate and solvate).

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    Sub Category: Polymorph & Crystal Screening
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    PHARMACEUTICAL SALT SCREENING

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    Eurofins offers physicochemical characterization of solid state APIs & advanced intermediates for expeditious discovery of pharmaceutical salts, solvates, co-crystals, particle size engineering by using High-Throughput Screening Technology (HTST).

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    Sub Category: Salt Screening
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    SOLUBILITY SCREENING STUDY

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    Eurofins CDMO offers fast & accurate solubility screenings for a large number of solvents while using minimum quantities of materials & solvents as starting materials, intermediates & APIs, by utilizing high-throughput robotic technology.

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    BIOLOGICAL DRUG SUBSTANCE MANUFACTURING

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    Eurofins CDMO provides integrated, end to end solutions for preclinical & clinical outsourcing services of both drug substance/API and drug product for biologicals and small molecules for pharmaceutical and biopharmaceutical companies.

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    Category: Biologics, Bioprocess & Fermentation

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    MANUFACTURING OF CLINICAL TRIAL BATCHES

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    Eurofins CDMO offers a full suite of drug development & manufacturing services encompassing the development of bioprocesses, pre-clinical testing, sterile and non-sterile bio-manufacturing of clinical trial batches, etc.

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    Category: Clinical Supply

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    CYTOTOXIC COMPOUND MANUFACTURING

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    Eurofins CDMO has state-of-the-art and dedicated cGMP cytotoxic facilities that are well-equipped with state of the art isolators to offer a diverse range of cytotoxic API chemical development & manufacturing solutions.

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    HIGH POTENT APIs (HPAPI) MANUFACTURING

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    Eurofins CDMO offers integrated contract manufacturing services through the entire drug product life cycle, including highly potent active pharmaceutical ingredients (HPAPIs). Its cGMP manufacturing facilities can handle highly potent APIs.

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    Category: High Potency APIs (HPAPIs)

    Sub Category: Overview
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    CONTRACT MANUFACTURING FOR PROTEINS & ENZYMES

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    Eurofins CDMO provides a full suite of drug manufacturing services for antibodies, proteins, enzymes, vaccines and different types of bacteria encompassing development of the bioprocesses, sterile & non-sterile bio-manufacturing of clinical trial batches.

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    Category: Protein / Peptide

    Sub Category: Overview
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    API SCALE-UP SERVICES

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    Eurofins operate multiple cGMP kilo laboratories to scale-up processes to the 50 litre scale for clinical and niche commercial APIs. They have cGMP manufacturing units which can support process volumes upwards of 500L to provide larger quantities of API.

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    Category: Scale Up

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    PACKAGING & LOGISTICS FOR CLINICAL SUPPLIES

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    With more than 30 years experience in packaging and logistics of clinical trial material, Eurofins CDMO offers packaging & logistics services with cold chain capacities to store, manage and distribute a wide range of clinical trial material.

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    Pharma Service: Clinical Trials

    Category: Packaging & Logistics

    Sub Category: Clinical Trial Supplies
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    COLD CHAIN CAPABILITIES

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    Eurofins CDMO has significant cold chain capacities enabling them to store, manage and distribute a wide range of clinical trial material. They have provided distribution to over 50 different countries including the U.S, India, Australia, Europe, etc.

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    Pharma Service: Clinical Trials

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    Sub Category: Cold Chain Solutions
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    PACKAGING & LABELING FOR CLINICAL SUPPLIES

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    Eurofins CDMO offers clinical trial supply activities, including primary & secondary packaging, labelling, storage, and worldwide distribution. They also support global studies from clinical phase I through to clinical phase III in packaging & logistics.

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    Pharma Service: Clinical Trials

    Category: Packaging & Logistics

    Sub Category: Packaging & Labeling
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    BIOAVAILABILITY ENHANCEMENT TECHNOLOGY

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    Eurofins offers various bioavailability enhancement drug delivery technologies for nanosuspensions, nanoformulations, S(M)EDDS, amorphous solid dispersions, co-micronization, co-spray drying, etc.

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    Pharma Service: Drug Product Manufacturing

    Category: Technologies

    Sub Category: Bioavailability Enhancement
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    CONTROLLED DRUG RELEASE TECHNOLOGY

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    Eurofins offers various controlled release drug delivery technologies including sustained or delayed release (colon targeting) using functional coatings (pellets, (mini)tablets) or matrix dosage forms (tablets, bilayered tablets).

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    Pharma Service: Drug Product Manufacturing

    Category: Technologies

    Sub Category: Controlled / Immediate / Modified Release
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    CONTROLLED RELEASE CAPSULE MANUFACTURING

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    Eurofins CDMO offers a wide range of drug product manufacturing such as manufacturing of immediate & controlled release capsules, tablets, bi-layered tablets, etc. They also offer commercial manufacturing for small commercial batches and orphan drugs.

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    Pharma Service: Drug Product Manufacturing

    Category: Capsule

    Sub Category: Controlled / Immediate / Modified Release
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    GEL MANUFACTURING

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    Eurofins offers development and manufacturing of semi solid dosage forms such as gel, cream, lotion, ointment for skin, mucosal or oral delivery. The developed drug products can be scaled-up for clinical trial manufacturing.

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    Pharma Service: Drug Product Manufacturing

    Category: Gel

    Sub Category: Overview
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    STERILE FILL & FINISH SERVICES

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    Eurofins CDMO offers sterile fill & finish activities for large and small molecule products under full global, GMP-compliance with finished dosage forms according to their customer requirements and drug product specifications.

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    Pharma Service: Drug Product Manufacturing

    Category: Injectable / Parenteral

    Sub Category: Overview
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    MANUFACTURING FOR STERILE INJECTABLES

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    Eurofins CDMO offers sterile manufacturing services to support lyophilized drug products. They also offer formulation transition from liquid to freeze dry form, freeze drying cycle development for HPAPI and cytotoxics up to OEL 4, BSL 2 products, etc.

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    Pharma Service: Drug Product Manufacturing

    Category: Injectable / Parenteral

    Sub Category: Controlled Substance
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    LIQUID DOSAGE FORMS FOR CLINICAL SUPPLY

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    Eurofins CDMO provides integrated, end-to-end drug development solutions supporting from the earliest clinical phases of API research and development through finished products of liquid dosage forms for oral, nasal, parenteral and ophthalmic delivery.

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    Pharma Service: Drug Product Manufacturing

    Category: Liquid

    Sub Category: Clinical Supply
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    LYOPHILIZED DRUG PRODUCT MANUFACTURING

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    Eurofins CDMO offers sterile manufacturing services to support lyophilized drug products such as formulation transition from liquid to freeze dry form, freeze drying cycle development for HPAPI and cytotoxics up to OEL 4, BSL 2 products, etc.

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    Pharma Service: Drug Product Manufacturing

    Category: Lyophilization

    Sub Category: Overview
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    CONTROLLED RELEASE TABLET MANUFACTURING

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    Eurofins CDMO offers a wide range of drug product manufacturing such as manufacturing of immediate & controlled release tablets, bi-layered tablets, capsules, etc. They also offer commercial manufacturing for small commercial batches and orphan drugs.

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    Pharma Service: Drug Product Manufacturing

    Category: Tablet

    Sub Category: Controlled / Immediate / Modified Release
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    BLISTER CONTRACT PACKAGING SERVICES

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    Eurofins CDMO provides the primary packaging services of non-sterile solid forms (capsules, tablets and over encapsulation) in HDPE blisters or bottles and in class C rooms with several options for caps (child proof, temper evident, desiccant).

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    Pharma Service: Packaging

    Category: Contract Services

    Sub Category: Blister
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    BOTTLE CONTRACT PACKAGING SERVICES

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    Eurofins CDMO can provide the primary packaging services of non-sterile solid forms (capsules, tablets and over encapsulation) in HDPE bottles or blisters and in class C rooms with several options for caps (child proof, temper evident, desiccant).

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    Pharma Service: Packaging

    Category: Contract Services

    Sub Category: Bottle
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    PREFILLED SYRINGES PACKAGING

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    Eurofins CDMO offers the secondary packaging of every clinical trial phases (I, II, III) for sterile & non-sterile dosage forms in pre filled syringes (PFS) & pens, blisters & blister-cards, bottles, medical devices, infusion kits, small packaging vials.

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    Pharma Service: Packaging

    Category: Contract Services

    Sub Category: Pre-Filled Syringe
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    CONTRACT SECONDARY PACKAGING SERVICES

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    Eurofins CDMO offers the secondary packaging of every clinical trial phases (I, II, III) for sterile & non-sterile dosage forms in blisters & blister-cards, bottles, pre filled syringes (PFS) & pens, medical devices, infusion kits, small packaging vials.

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    Pharma Service: Packaging

    Category: Contract Services

    Sub Category: Secondary Packaging
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    VIALS CONTRACT PACKAGING

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    Eurofins CDMO offers the secondary packaging of every clinical trial phases (I, II, III) for sterile & non-sterile dosage forms in small packaging vials, infusion kits, blisters & blister-cards, bottles, pre filled syringes (PFS) & pens, medical devices.

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    Pharma Service: Packaging

    Category: Contract Services

    Sub Category: Vial
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    PEPTIDE DEVELOPMENT & BIOMANUFACTURING

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    Eurofins CDMO offers custom peptide services such as peptide development and manufacturing for complex peptide APIs. Its peptide capabilities include custom peptide synthesis, peptide API development, peptide biomanufacturing & peptide drug development.

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Protein / Peptide
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    SMALL MOLECULE API DEVELOPMENT SERVICES

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    Eurofins CDMO provides drug substance development services with pharmaceutical and biotechnology applications for complex small molecule API programs from preclinical to phase III and commercial manufacturing.

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Small Molecules
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    SMALL MOLECULE API MANUFACTURING

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    Eurofins CDMO offers small molecule API manufacturing and development services with pharmaceutical and biotechnology applications for complex, niche, small molecule programs from preclinical to phase III and commercial manufacturing.

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    Pharma Service: API Manufacturing

    Category: Small Molecules

    Sub Category: Overview
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    DEVELOPMENT OF COMPLEX SMALL MOLECULE APIs

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    Eurofins CDMO Alphora is a full service contract research, development and manufacturing organization for complex and niche small molecule active pharmaceutical ingredients (APIs).

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Complex APIs
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