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    Pharma Services Category of UQUIFA

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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 (3)

    02 Analytical Method Development (1)

    03 Chiral Synthesis (1)

    04 Clinical Supply (1)

    05 Fine Chemical / Intermediate (1)

    06 GMP Manufacturing (1)

    07 Halogenation (1)

    08 Hydrogenation (1)

    09 Lyophilization (1)

    10 Organometallic Chemistry (1)

    11 Ozonolysis (1)

    12 Preformulation & Material Science (1)

    13 Reference Standard (1)

    14 Regulatory Affairs / Pharmacovigilance (1)

    15 Scale Up (2)

    16 Small Scale Batch (1)

    17 Stability Studies (1)

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    01 UQUIFA (20)

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    UQUIFA

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    STABILITY STUDIES

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    Uquifa has capabilities for stability studies, impurity profile characterization, process transfer, reference standards synthesis, process transfer, polymorphism studies,etc.

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    Pharma Service: Analytical

    Category: Stability Studies

    Sub Category: Overview
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    ANALYTICAL METHOD VALIDATION

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    Uquifa has capabilities for analytical method validation, stability studies, process validation, working standard supply, scale up to commercial, process transfer, etc.

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    Pharma Service: Analytical

    Category: Analytical Method Development

    Sub Category: Method Development and Validation
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    IMPURITY PROFILE CHARACTERIZATION

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    Uquifa is a leading company for APIs and advanced intermediates offering capabilities including impurity profile characterization, stability studies, process validation and analytical method development services.

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Impurity / Reference Standard
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    POLYMORPHISM STUDIES

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    Uquifa offers polymorphism studies, stability studies, scale up, analytical method validation, working standard supply, impurity profile characterisation,etc.

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    Pharma Service: API & Drug Product Development

    Category: Preformulation & Material Science

    Sub Category: Polymorph & Crystal Screening
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    ADVANCED INTERMEDIATE DEVELOPMENT

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    Uquifa is a leading company for API and advanced intermediate development and manufacturing. They can offer R&D and cGMP compliant manufacturing across two continents, America and Europe.

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Fine Chemical / Intermediate
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    SYNTHETIC ROUTE DEVELOPMENT

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    Uquifa offers the development of novel synthetic routes with the team working on the development and transfer of chemical processes suitable for the efficient manufacture of APIs and key intermediates.

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    Pharma Service: API & Drug Product Development

    Category: API Development

    Sub Category: Route Evaluation & Development
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    GMP COMPLIANT MANUFACTURING

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    Uquifa is a leading company for API and advanced intermediate development and manufacturing. They can offer R&D and cGMP compliant manufacturing across two continents, America and Europe.

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    Pharma Service: API Manufacturing

    Category: GMP Manufacturing

    Sub Category: Overview
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    PROCESS DEVELOPMENT, OPTIMIZATION & TRANSFER

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    Uquifa offers process development and improvement, stability studies, method validation, process transfer, impurity characterization, scale up to commercial, etc.

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    Pharma Service: API Manufacturing

    Category: Scale Up

    Sub Category: Overview
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    SCALE-UP FROM PILOT PLANT TO COMMERCIAL SCALE

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    Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services including DMF/CTD/COS application, stability studies, process validation and analytical method validation, working standard supply or impurity,

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    Pharma Service: API Manufacturing

    Category: Scale Up

    Sub Category: Overview
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    REFERENCE STANDARD SYNTHESIS

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    Uquifa provides opportunities to manage the development activities of any drug life cycle by offering capabilities for reference standards synthesis, stability studies, process validation and analytical method validation, working standard supply, etc.

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    Pharma Service: API Manufacturing

    Category: Reference Standard

    Sub Category: Overview
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    SMALL SCALE API & NCE PRODUCTION

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    Uquifa works on the development & transfer of chemical processes suitable for the efficient manufacture of APIs & key intermediates, synthesizing products from 1 g to 1 kg and developing processes which are scalable, safe & environmentally friendly.

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    Pharma Service: API Manufacturing

    Category: Small Scale Batch

    Sub Category: Overview
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    OZONOLYSIS REACTIONS

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    Uquifa's production units are designed to be flexible, allowing many combinations of reactors, filters & dryers to perform reactions that are conducted at industrial scale, reactions such as ozonolysis, nitrations, hydrogenations, etc.

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    Pharma Service: API Manufacturing

    Category: Ozonolysis

    Sub Category: Overview
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    HYDROGENATION REACTIONS

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    Uquifa's production units are designed to be flexible allowing many combinations to be used in order to perform the same type of reactions that are conducted at an industrial scale. Reactions such as hydrogenation, nitration and ozonolysis are performed.

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    Pharma Service: API Manufacturing

    Category: Hydrogenation

    Sub Category: Overview
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    PHARMACEUTICAL INTERMEDIATE MANUFACTURING

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    Uquifa is a contract manufacturer of Active Pharmaceutical Ingredients (APIs) & intermediates for the pharmaceutical & animal health industries globally. It has been inspected & approved by leading global pharmaceutical companies & regulatory authorities.

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    Pharma Service: API Manufacturing

    Category: Fine Chemical / Intermediate

    Sub Category: Overview
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    API MANUFACTURING FOR CLINICAL SUPPLY

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    Uquifa has pilot plants producing 1 kg to multi-kg quantities for preclinical & clinical trials and for small scale commercial production. Large commercial scale batches are produced at the manufacturing plants after validation runs have been completed.

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    Pharma Service: API Manufacturing

    Category: Clinical Supply

    Sub Category: Overview
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    FREEZE DRYING (LYOPHILIZATION)

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    Uquifa's technical tool box has various equipment and reactors for freeze drying (lyophilization), centrifugation, micronisation, compaction, pellets formulation, ozone generator, etc.

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    Pharma Service: API Manufacturing

    Category: Lyophilization

    Sub Category: Overview
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    HALOGENATION REACTIONS

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    Uquifa engages with many pharmaceutical and animal health companies to manufacture products for both human and animal health use with chemical expertise in bromination & nitration reactions, sulfur chemistry, borane derivatives, etc.

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    Pharma Service: API Manufacturing

    Category: Halogenation

    Sub Category: Overview
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    CHIRAL ASYMMETRIC SYNTHESIS

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    Uquifa manufactures products for both human and animal health use with chemical expertise in chiral – asymmetric synthesis, sulfur chemistry, borane derivatives, etc.

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    Pharma Service: API Manufacturing

    Category: Chiral Synthesis

    Sub Category: Overview
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    ORGANOMETALLIC REACTIONS

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    Uquifa engages with many pharmaceutical & animal health companies to manufacture products for both human & animal health use with chemical expertise in grignard & organometallic reactions, triphosgene reactions, sulfur chemistry, borane derivatives, etc.

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    Pharma Service: API Manufacturing

    Category: Organometallic Chemistry

    Sub Category: Overview
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    REGULATORY SUPPORT & VALIDATION

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    Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering capabilities for regulatory support and file submission and maintenance, stability studies, working standard supply or impurity characterization.

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    Pharma Service: Sales, Marketing, Registration

    Category: Regulatory Affairs / Pharmacovigilance

    Sub Category: Spain
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