Centralized management of quality documents with i-ShareDX for pharmaceuticals and biotechnology.
Share the latest version of the manufacturing, sterilization, and inspection procedures to standardize quality control and on-site training!
In the research and manufacturing fields of pharmaceuticals and cosmetics, it is necessary to accurately manage many documents, such as manufacturing procedures, sterilization and cleaning methods, clean room management standards, and packaging and inspection procedures. However, if SOPs, work instructions, and quality-related documents are scattered across paper, PDFs, and shared folders, it takes time to confirm the latest versions, leading to references to outdated procedures and variations in training content. i-ShareDX is a document management system that centrally manages manuals and regulations related to research, manufacturing, packaging, and quality control in the cloud. It allows for immediate access to necessary documents through category and full-text searches, and supports review and approval, version control, and access rights settings. It ensures that revisions related to changes in equipment, processes, and inspection methods are reliably shared with stakeholders, supporting the proper operation of quality documents, standardization of work, and reduction of training burdens.
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【Features】 - Centralized management of manufacturing procedures, SOPs, quality standards, and training materials in the cloud - Sharing of procedures for sterilization, cleaning, sanitation, and cleanroom management - Management of operation manuals for manufacturing equipment, packaging machinery, and measurement/testing devices - Quick access to necessary documents through category search and full-text search - Content review before publication through review and approval functions - Ensured sharing of the latest version through version management and revision history recording - Setting of viewing permissions based on research, manufacturing, quality control, factory, and responsibilities - Smooth navigation to related procedures and quality standards through inter-document links - Accessible from computers and tablets in research and manufacturing sites 【Our Strengths】 Since our founding in 1947, we have provided a wide range of solutions from manual production, web, systems, to marketing, based on the "communication technology" cultivated through printing. We help organize complex manufacturing and quality management procedures in an easy-to-understand manner, supporting document structure design, manual standardization, and operations after system implementation.
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![[Information] Streamlining the often complicated maintenance and management of ISO document operations.](https://image.mono.ipros.com/public/catalog/image/385453/IPROS14589843105077637008.jpeg?w=120&h=170)
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Quix has clarified what should be changed and what should not be changed, inheriting the spirit of "eternal change" and has developed in response to the changes of the times since its founding. Recently, due to the evolution of IT such as digitalization, networking, and cross-media, the form of "information" we handle continues to change at a rapid pace. It is precisely in this context that we want to re-examine the "information expression technology" we have cultivated over many years, enhance and diversify it, and contribute to our customers and society by fulfilling our mission of "creating and promoting communication." We will advance our corporate philosophy of "creating services that bring joy" by focusing on support services in the three areas we are currently working on: "manuals," "education," and "sales promotion." We are determined to aim to be a "CS No.1" company that is recognized as a true business partner capable of solving various problems while being a company that customers can trust and rely on for "safety and trust."
