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Pharmaceutical manufacturing services

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last updated:Mar 01, 2023

片山製薬所
片山製薬所
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Accumulating about 50 types of organic synthesis techniques. Supporting the pharmaceutical business from development to market launch.

We provide comprehensive support for the pharmaceutical business, from process development to prototyping and full-scale production. We flexibly and swiftly respond to a wide range of needs, including the exploration of synthetic routes for target compounds, sample synthesis, production of intermediates and active pharmaceutical ingredients under development, support for approval applications of developed products, and large-scale production of active pharmaceutical ingredients after market launch. We fully support your pharmaceutical business. Please feel free to contact us with your requests. 【Support Services】 ■ Research and Development Support - Development of synthetic routes - Manufacturing process development and scale-up considerations - Process safety evaluations ■ Manufacturing Support *For more details, please download the PDF or feel free to contact us.

    Pharmaceutical intermediate manufacturing services
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Pharmaceutical manufacturing services

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  • Related Link - https://www.katayama-finechem.co.jp/

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【Features】 ■Quality Assurance System  ・Strict validation implemented for all equipment and processes ■GMP System  ・Global GMP system recognized by authorities in Europe and the United States ■Research System  ・Appropriate proposals based on cultivated knowledge and technical expertise *For more details, please download the PDF or feel free to contact us.

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Katayama Pharmaceutical Co., Ltd. Company Profile

Katayama Pharmaceutical Co., Ltd. Company Profile

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片山製薬所

片山製薬所

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Since our establishment in 1922, we have been developing our business in the manufacturing of photographic printing paper chemicals, fine chemicals, and contract manufacturing of pharmaceutical active ingredients and intermediates. During this time, we have built a cGMP-compliant pharmaceutical manufacturing management system and have undergone GMP inspections by the US FDA, European AIFA (EMA), and Japan's PMDA, earning high evaluations and trust from many pharmaceutical companies as a CMO capable of supporting all three regions. In the future, we will continue to strive to be a partner in "medicine manufacturing" by expanding our facilities, enhancing our process development capabilities, and improving our technical services. Please feel free to contact us with any requests.

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