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    Pharma Services Category of UPM Pharmaceuticals

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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 Analytical Method Development (1)

    02 Analytical Testing Services (5)

    03 Capsule (2)

    04 Contract Services (5)

    05 Cream / Lotion / Ointment (1)

    06 Formulation Development (4)

    07 Stability Studies (1)

    08 Tablet (2)

    09 Technologies (1)

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    01 UPM Pharmaceuticals (22)

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    01 U.S.A (22)

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    UPM Pharmaceuticals

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    WET AND DRY GRANULATION TECHNIQUES

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    UPM has extensive experience and expertise in formulation development capabilities include blending, high shear granulation, fluid bed granulation technology, extrusion-spheronization, roller compaction, bi-layer compression, etc.

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    Pharma Service: Drug Product Manufacturing

    Category: Technologies

    Sub Category: Granulation & Extrusion
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    IMMEDIATE RELEASE SOLID ORAL DOSAGE FORMS

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    UPM has extensive experience and oral drug delivery expertise in the formulation development of solid oral dosage forms, including immediate and controlled release formulations (tablet/capsule).

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    Pharma Service: API & Drug Product Development

    Category: Formulation Development

    Sub Category: Controlled / Immediate / Modified Release
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    BILAYER, COATED, ENCAPSULATED MINI TABLETS

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    Formulation development capabilities include blending, high shear granulation, fluid bed granulation, extrusion-spheronization, roller compaction, bi-layer compression, mini-tablets, encapsulated tablets and beads, coated tablets.

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    Pharma Service: API & Drug Product Development

    Category: Formulation Development

    Sub Category: Tablet
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    TOPICAL FORMULATIONS

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    UPM also has expertis with development, testing, formulation and manufacture of semi-solid drugs, including creams and ointments

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    Pharma Service: API & Drug Product Development

    Category: Formulation Development

    Sub Category: Cream / Gel / Lotion / Ointment
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    TECHNOLOGY TRANSFER FOR DEVELOPMENTAL PROCESSES

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    UPM’s analytical group has a diverse background in analytical method development and in-depth understanding of all facets of the drug development process.

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    Pharma Service: API & Drug Product Development

    Category: Formulation Development

    Sub Category: Tech Transfer
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    MICROBIAL TESTING

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    UPM’s analytical group has a diverse background in analytical method development and in-depth understanding of all facets of the drug development process.

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    Pharma Service: Analytical

    Category: Analytical Testing Services

    Sub Category: Microbiology
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    PURITY TESTING

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    UPM’s analytical group has a diverse background in analytical method development and in-depth understanding of all facets of the drug development process.

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    Pharma Service: Analytical

    Category: Analytical Method Development

    Sub Category: Impurity Isolation and Identification
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    FULL ICH STABILITY CONDITIONS

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    UPM’s analytical group has a diverse background in analytical method development and in-depth understanding of all facets of the drug development process.

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    Pharma Service: Analytical

    Category: Stability Studies

    Sub Category: Overview
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    PARTICLE SIZE DETERMINATION BY LASER

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    UPM’s analytical group has a diverse background in analytical method development and in-depth understanding of all facets of the drug development process.

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    Pharma Service: Analytical

    Category: Analytical Testing Services

    Sub Category: Particle Size
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    GC -HEADSPACE, HPLC & UPLC WITH DUAL WAVE PDA DETECTORS

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    UPM’s analytical group has a diverse background in analytical method development and in-depth understanding of all facets of the drug development process.

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    Pharma Service: Analytical

    Category: Analytical Testing Services

    Sub Category: Chromatography (TLC / LC / HPLC / UPLC / GC)
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    DRUG RELEASE TESTING BY DISSOLUTION STUDIES

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    UPM’s analytical group has a diverse background in analytical method development and in-depth understanding of all facets of the drug development process.

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    Pharma Service: Analytical

    Category: Analytical Testing Services

    Sub Category: Dissolution
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    PARTICLE SIZE ANALYZERS & 3 TOC ANALYZERS

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    UPM’s analytical group has a diverse background in analytical method development and in-depth understanding of all facets of the drug development process.

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    Pharma Service: Analytical

    Category: Analytical Testing Services

    Sub Category: Particle Size
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    COMMERCIAL MANUFACTURING OF TABLETS

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    UPM Pharmaceutical’s commercial manufacturing facility encompasses 475,000 square feet on almost seven acres. This facility provides UPM with large scale commercial capabilities for manufacturing and packaging of solid oral dosage tablets and capsules, as well as semi-solid manufacturing

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    Pharma Service: Drug Product Manufacturing

    Category: Tablet

    Sub Category: Overview
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    SEMI-SOLID BULK MANUFACTURING & PACKAGING

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    UPM's manufacturing facility encompasses 475,000 square feet on almost seven acres. This facility provides UPM with large scale commercial capabilities for bulk manufacturing & packaging solid oral tablets & capsules, as well as semi-solid manufacturing.

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    Pharma Service: Drug Product Manufacturing

    Category: Cream / Lotion / Ointment

    Sub Category: Overview
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    COMMERCIAL MANUFACTURING OF CAPSULES

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    UPM Pharmaceutical’s commercial manufacturing facility encompasses 475,000 square feet on almost seven acres. This facility provides UPM with large scale commercial capabilities for manufacturing and packaging of solid oral dosage tablets and capsules, as well as semi-solid manufacturing

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    Pharma Service: Drug Product Manufacturing

    Category: Capsule

    Sub Category: Overview
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    cGMP MANUFACTURING OF TABLET FOR CLINICAL PHASES

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    UPM provides cGMP manufacturing for clinical Phase I, II, and III products, including tablets, capsules and semi-solids. We are capable of producing batch sizes ranging from a few thousand units to over a million units per batch.

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    Pharma Service: Drug Product Manufacturing

    Category: Tablet

    Sub Category: Clinical Supply
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    cGMP MANUFACTURING OF CAPSULE FOR CLINICAL PHASES

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    UPM provides cGMP manufacturing for clinical Phase I, II, and III products, including tablets, capsules and semi-solids. We are capable of producing batch sizes ranging from a few thousand units to over a million units per batch.

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    Pharma Service: Drug Product Manufacturing

    Category: Capsule

    Sub Category: Clinical Supply
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    PACKAGING SERVICES FOR SOLID & SEMI-SOLID DOSAGE FORMS

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    We have packaging capabilities for filling of tablets and capsules into bottles; and filling of semi-solids into jars and tubes. We have an additional site with 300,000 square feet of warehousing space.

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    Pharma Service: Packaging

    Category: Contract Services

    Sub Category: Overview
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    BOTTLING FOR TABLETS & CAPSULES

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    We have packaging capabilities for filling of tablets and capsules into bottles; and filling of semi-solids into jars and tubes. We have an additional site with 300,000 square feet of warehousing space.

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    Pharma Service: Packaging

    Category: Contract Services

    Sub Category: Bottle
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    JARS FOR SEMI SOLID PREPARATIONS

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    We have packaging capabilities for filling of tablets and capsules into bottles; and filling of semi-solids into jars and tubes. We have an additional site with 300,000 square feet of warehousing space.

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    Pharma Service: Packaging

    Category: Contract Services

    Sub Category: Jar
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    TUBES FOR SEMI SOLID PREPARATIONS

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    We have packaging capabilities for filling of tablets and capsules into bottles; and filling of semi-solids into jars and tubes. We have an additional site with 300,000 square feet of warehousing space.

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    Pharma Service: Packaging

    Category: Contract Services

    Sub Category: Tube
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    PACKAGING FOR CONTROLLED SUBSTANCES

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    UPM offers handling and packaging of DEA Schedule I–V controlled substances. With over 15,800 square feet of approved vault space, an extensive track record of controlled substance is maintained.

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    Pharma Service: Packaging

    Category: Contract Services

    Sub Category: Controlled Substance
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