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  6. [Technology and Achievements] Setting Manufacturing Methods According to Development Stages

[Technology and Achievements] Setting Manufacturing Methods According to Development Stages

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last updated:May 19, 2022

スペラファーマ
スペラファーマ
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Examples of cost reduction and high-activity compounds explained with diagrams! We have succeeded in minimizing the containment process.

Sperapharma builds and proposes manufacturing methods that satisfy customer needs. The manufacturing methods for active pharmaceutical ingredients vary depending on the development stage and situation of the compounds, with different needs generally arising at different stages: speed is prioritized in the early development phase, robustness and R&D cost reduction in the mid-phase, and commercial cost competitiveness and advanced process management strategy development in the late phase. Our company designs manufacturing routes based on structure-activity relationships and has succeeded in minimizing containment processes. This has enabled flexible manufacturing, shortened production times, reduced costs, alleviated workload, and decreased environmental impact. We have illustrated examples of cost reduction and cases involving highly active compounds, which you can view through the related links below. 【Features】 ■ Implementation of manufacturing route design based on structure-activity relationships ■ Successful minimization of containment processes ■ Achieved flexible manufacturing, shortened production times, reduced costs, alleviated workload, and decreased environmental impact *For more details, please refer to the PDF materials or feel free to contact us.

    Other contract servicesTechnology Development
2022-05-18_15h56_09.png

[Technology and Achievements] Setting Manufacturing Methods According to Development Stages

2022-05-18_15h56_09.png
2022-05-18_15h56_09.png
  • Related Link - https://www.spera-pharma.co.jp/technology/drug/dev…

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Sperapharma Co., Ltd. Company Profile

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[Web Seminar] Equipment Design for Continuous Production of Active Pharmaceutical Ingredients / Process Integration and GMP Compliance

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Mitsuhiro Yamano from our Pharmaceutical Research Headquarters will be speaking at the seminar hosted by the Technical Information Association titled "Equipment Design/Process Integration and GMP Compliance in Continuous Production of Active Pharmaceutical Ingredients," in Part 3. Under the title "Challenges and Prospects for Implementing Continuous Production of Active Pharmaceutical Ingredients - Aiming for Application to GMP Processes," he plans to discuss the challenges of implementing continuous production, which has recently garnered attention, in the context of active pharmaceutical ingredients. Event Details: Date: June 20, 2022 (Monday) 10:00 AM - 5:00 PM Venue: Live streaming via Zoom (No in-person lectures will be held) Participation Fee: 60,500 yen per person (including tax and materials) [55,000 yen per person if two or more participants from the same company register simultaneously] For more details, please check with the Technical Information Association or visit our website. https://www.gijutu.co.jp/doc/s_206114.htm

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スペラファーマ

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Our company is a pharmaceutical CMC research and development contract company that spun out from the CMC research division of Takeda Pharmaceutical Company Limited in July 2017. We support excellent pharmaceutical development as experts in CMC research. Our research team consists of experts with extensive experience and achievements in process chemistry, formulation research and development, and analytical testing development related to CMC research. We provide high-level services and solutions tailored to our customers' needs across each process from the early stages of pharmaceutical development to application, while flexibly collaborating. We have established a collaborative system with partner companies, enabling us to offer a one-stop service. Please utilize us as a platform for your pharmaceutical development.

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