シーエーシー List of Products and Services

Our company offers a "GxP-compliant cloud archive environment construction and operation service" that strongly supports pharmaceutical companies in utilizing cloud archives. We provide CSV support during the construction of the cloud archive environment and also handle CSV-compliant operations after the service begins. We will propose a combination of AWS services that are well-suited to solving our customers' challenges, including operational support.

• Other Software

"RETIP" is a solution that supports drug discovery research operations involving compound samples. It consists of a "Sample Management System" that assists in managing inventory information such as the location and remaining quantity of compound samples, as well as various preparation tasks, and a "Test Request System" that supports the request and acceptance of tests. The "Sample Management System" is equipped with request forms that cater to various sample preparation tasks such as receiving, shipping, weighing, and plate preparation. It allows for the management of requests from initiation to completion, enabling researchers and administrators to share the progress of requests. Additionally, it centralizes inventory information managed by researchers, departments, or external contractors, facilitating accurate understanding of inventory status. The "Test Request System" allows users to register frequently used tests and related test sets, enabling the specification of related test items in bulk when making requests, thus preventing omissions in necessary test requests. It also features a duplicate check function that displays alerts for tests that have been conducted in the past, preventing duplicate requests. Both systems conduct usage restriction checks based on regulatory information during preparation and test requests, thereby reducing the risk of legal violations.

• Other production and development software and systems

We offer a sales support system, MR-Navi (SFA/CRM), Promotion Mail, actual consumption solutions, and comprehensive sales master management features at a low price, with a proven track record among numerous pharmaceutical companies. - Customization of features is possible through changes in function settings. - We will continuously upgrade the system to align with industry trends. - No need to purchase or register facility masters; you can start using it immediately. - It is also compatible with data integration with internal systems. - The system can be ready for use in as little as two weeks from application. - We offer a subscription-based contract format for your convenience.

• Other production and development software and systems
• Other IT tools

"PLACT" is a system that supports a series of tasks from the application for animal experimentation plans to breeding management and final reporting. It allows for centralized management of information related to animal management tasks. The system facilitates smooth information sharing among stakeholders, thereby reducing the workload. It is possible to implement either the "Animal Experiment Review System" or the "Animal Breeding Management System" alone, and it also makes it easy to respond to investigations from third-party organizations. [Features] ■ The system properly executes and records the application and approval procedures for plans. ■ Ensures compliance with the Ministry of Health, Labour and Welfare guidelines and consideration for animal welfare. ■ Makes it easy to respond to investigations from third-party organizations. ■ Centralized management of information related to animal management tasks. ■ Supports flexible system implementation tailored to needs and environments. *For more details, please refer to the PDF materials or feel free to contact us.

• Other production and development software and systems

Our company offers "CSV-compliant cloud environment construction and operation services." We propose the migration and operation to the cloud of on-premises business systems and files/data managed on-premises, while considering data integrity. Members who are well-versed in the requirements of pharmaceutical industry systems and various regulations and guidelines such as GxP will provide support. From planning to design, you can leave the cloud migration, including CSV, to CAC.

• File Management
• Other contract services