CM Plus prepared a URB (User Requirements Brief) for the production volume of the product to be manufactured (pharmaceutical labels), the utility conditions of the production facility, and the requirements for the facility and equipment.

In the conceptual design phase, CM Plus worked with the client on a land use plan that took into account future concepts in the site utilization plan, and studied the layout plan (first phase plan).
In order to realize one of the project concepts, “meeting global quality requirements” we adopted a concept that conforms to GMP-compliant facilities.
Specifically, we aimed for the quality of a pharmaceutical plant, with clear and step-by-step area separation, air conditioning, insect control, and a product transfer system/plan and cross-sectional plan that links the automated warehouse and production system.

In order to get the project right, we provided a rough estimate and assisted the client in developing a budget.

At the construction inquiry stage, CM Plus prepared specifications and books for quotation inquiries with clear specifications. This made it possible to conduct quotations from multiple construction companies and evaluate their quotations fairly.
In selecting a construction company, we evaluated the cost and technical evaluation using a comparison table, and conducted interviews with each company together with the client to select the best construction company.

During the construction phase, we attended regular meetings held at the site and contributed to ensuring good construction quality by supervising construction progress, checking construction quality, confirming changes, and assessing additional construction costs.

After the operation started, we have been informed that many end-user pharmaceutical manufacturers have commented that the plant complies with GMP in their manufacturing process (labeling) inspections and plant inspections, and we believe that the plant meets the needs of our customers.