We will consider not only the hardware aspect but also the software aspect from a practical perspective! We will help resolve your concerns.
We will support you in preventing "cross-contamination" at your pharmaceutical manufacturing facility from a position that aligns with your company. Are there any issues such as "the same staff member is responsible for both weighing tasks and the manufacturing of different products" or "multiple production equipment for different products are installed in the same manufacturing room"? Our experienced engineers will carefully identify the issues by conducting on-site investigations and interviewing workers about your current situation. We will share the identified issues with you as challenges and decide on a course of action for solutions. 【Do you have any such challenges?】 ■ There have been comments related to cross-contamination during inspections, and upper management is urging consideration of countermeasures. ■ You would like to receive support from knowledgeable and experienced experts regarding the current evaluation of cross-contamination and future enhancements. ■ You want to implement necessary minimum measures while keeping the budget in check. *For more details, please refer to the PDF document or feel free to contact us.
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【Situations Prone to Cross-Contamination】 ■ Powder that has flowed out from the manufacturing room is adhering to the floor. ■ The same staff member is responsible for both weighing operations and the production of different products. ■ Residual powder from previous operations is remaining and accumulating in the process room (floor, stage, air conditioning intake). ■ Multiple production machines handling different products are installed in the same manufacturing room. ■ A large room is divided by simple partitions and used for different purposes. *For more details, please refer to the PDF document or feel free to contact us.
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[Examples of Achievements] ■ Existing factory that manufactures a variety of solid dosage forms *For more details, please refer to the PDF document or feel free to contact us.
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Our company was founded in September 2012 and specializes in engineering services that include validation and calibration, focusing on consulting, planning, design, and construction related to the establishment and renovation of pharmaceutical manufacturing facilities and research facilities based on GxP. With the motto of "User's Engineering," we prioritize the quality of pharmaceuticals and work closely with our clients involved in pharmaceutical manufacturing. We emphasize practicality and feasibility, collaborating with our clients to visualize and solve the challenges faced by each manufacturing site.