IT Transformation in Indirect Departments and Factory Sites for the Pharmaceutical Industry
Achieving efficiency in both the field and indirect departments through IT implementation that supports GMP compliance.
In the pharmaceutical industry, strict adherence to GMP (Good Manufacturing Practice) standards is required to ensure product quality and safety. In particular, ensuring traceability in the manufacturing process and streamlining document management and approval processes in indirect departments are emphasized for both compliance and operational execution. Inadequate management poses risks of product quality issues and feedback from regulatory authorities. Our IT support aims to address these challenges by enhancing efficiency on the ground, reducing labor in indirect departments, and improving operational efficiency through the use of generative AI, thereby supporting GMP compliance and striving to establish a sustainable manufacturing system. 【Usage Scenarios】 - Real-time data collection and recording on the production line - Digitization of quality control documents and access management - Automation of approval workflows and progress management - Support for report creation using generative AI 【Benefits of Implementation】 - Improved compliance with GMP standards - Reduction of human errors and enhancement of data accuracy - Acceleration of business processes and shortening of lead times - Strengthening of compliance and risk reduction
- Company：ヴィサイプ
- Price：Other
