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    Pharma Services Category of ACTA Laboratories Inc

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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 (6)

    03 Stability Studies (1)

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    01 ACTA Laboratories Inc (8)

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    ACTA Laboratories Inc

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      ANALYTICAL SERVICES - GC ANALYSIS & TESTING

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      ACTA Laboratories is an analytical testing laboratory offering pharmaceutical analysis for APIs & drug products. Its analytical services include GC & HPLC testing, analytical chemistry, method validation along with other analytical testing services.

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      Pharma Service: Analytical

      Category: Analytical Testing Services

      Sub Category: Chromatography (TLC / LC / HPLC / UPLC / GC)
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        HPLC ANALYSIS & TESTING

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        ACTA Laboratories, Inc. is a cGMP FDA Registered Testing Laboratory that performs HPLC analyses on Pharmaceutical APIs (Active Pharmaceutical Ingredients) and Drug Products. ACTA can follow USP, BP, JP, and EP methods or develop methods of analysis for your API or Drug Product.

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        Pharma Service: Analytical

        Category: Analytical Testing Services

        Sub Category: Chromatography (TLC / LC / HPLC / UPLC / GC)
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          HEAVY METALS TESTING USP <231>, <232>, AND <233>

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          ACTA Laboratories, Inc. is a cGMP FDA Registered Testing Laboratory that performs USP <231> (wet chemistry testing for heavy metals) and USP <232>/<233> (ICP-MS testing for Elemental Impurities) on Pharmaceutical APIs (Active Pharmaceutical Ingredients) and Drug Products.

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          Pharma Service: Analytical

          Category: Analytical Testing Services

          Sub Category: Trace / Elemental / Heavy Metals
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            USP <231> HEAVY METALS TESTING

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            The current procedure in the USP for Heavy Metals testing is a wet chemistry test that utilizes sulfide to precipitate certain heavy metals (Pb, Hg, Bi, As, Sb, Sn, Cd, Ag, Cu, and Mo). The test sample preparation is visually examined to see if it is darker than the standard.

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            Pharma Service: Analytical

            Category: Analytical Testing Services

            Sub Category: Trace / Elemental / Heavy Metals
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              USP <232> ELEMENTAL IMPURITIES – LIMITS

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              The new ICP-MS procedures are quantitative and will provide an accurate assessment of elemental impurities. The USP <232> Elemental Impurities Limits lists the proposed limits for allowable levels of elemental impurities in drug products and drug substances.

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              Pharma Service: Analytical

              Category: Analytical Testing Services

              Sub Category: Trace / Elemental / Heavy Metals
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                cGMP MICROBIOLOGICAL TESTING

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                ACTA offers comprehensive microbiological services to support your needs. ACTA uses well-maintained and calibrated instrumentation to perform your microbiological testing.

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                Pharma Service: Analytical

                Category: Analytical Testing Services

                Sub Category: Microbiology
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                  cGMP COMPLIANT STABILITY STUDY PROTOCOLS

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                  ACTA can write stability protocols for you or provide assistance to ensure your stability projects are fully cGMP compliant and meet the stringent requirements of the FDA. ACTA tracks your stability projects carefully to ensure that they are tested in a timely manner.

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                  Pharma Service: Analytical

                  Category: Stability Studies

                  Sub Category: Overview
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                    cGMP METHOD VALIDATION & DEVELOPMENT

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                    ACTA performs cGMP method validation in accordance with USP and ICH requirements. Parameters normally validated are accuracy, precision, specificity, limit of detection, limit of quantitation, linearity, range and robustness. ACTA’s staff is highly experienced with method development for

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                    Pharma Service: Analytical

                    Category: Analytical Method Development

                    Sub Category: Method Development and Validation
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