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Digital Transformation, where are you?
Adiuto solutions for your Business
Adiuto enables its stakeholders' digital transformation by raising their degree of resilience, and bringing innovation to their value chain, without additional costs in terms of change management and time wasting. The Adiuto platform allows the digitization and simplification of complex processes, thanks to its powerful Workflow engine and the simple and intuitive management of documents.
Management of both GxP and non-GxP documentation. Publication and centralized consultation of analysis certificates (created on special Adiuto external systems), approval flows of quality system documents (procedures and forms). Data collection processes (CAPA, deviations) of the quality system. Management of data related to the training of Quality area personnel (ongoing project).
Complete management of the patient hospitalization process, from booking to discharge, which includes clinical and administrative management with related documentation. Active and passive management of the entire administrative cycle, including medical professional invoices, B2B (passive flow).
The system is used for the management of both GxP critical and non-GXP documents. Digitization of approval flows of procedures, forms, and production documentation (Master Batch Record). Digitization of the Change Control Management Process, Management of the quality manual and monographs, management of information related to human resources training in the implementation phase.
Digitization of document approval and process flows in different units belonging to Recipharm Italia, in compliance with EU-GMP Annex 11 and FDA-CFR 21 Part 11 regulations. Procedures and Forms, MBR, CAPA, Change Control, Deviations, Complaints. "Technical Customers Services" solution: in response to customer requests, the system allows activities to be assigned to the various corporate bodies involved. The activities, parallel or sequential, are mapped to the system, ensuring traceability until the request has been processed. ArtWorks Management Flow.
Complete management of the administrative cycle and transversal approval flows, signature collection with graphometric tablet for internal sales and for the collection of privacy, Expense Report Management, Digital Preservation according to regulations and B2B.
Management of the administrative cycle, with strong parameterization and customization of the active cycle in sending invoices, management of the passive cycle with authorization workflow and non-compliance management, parametric for the group's 15 companies. Integration with SAP and SAP VIM, regulatory compliance, and B2B.
Document management of orders, with classification and parameterization of permissions. Management of the supplier qualification process with CMS integration for supplier access during data entry phase and documents. Management of specialized courses for employee certifications.
Management of GxP quality processes, validated according to Annex 11 and CFR 21. Digitization of ”customer complaints" management, starting from reporting, investigation, and the opening of any corrective actions, with the involvement of pharmacovigilance, where necessary. Digital document signing flow. Involvement of external stakeholders (suppliers) in the supplier qualification process, with enterprise ERP SAP integrations.
Management of both GxP and non-GxP documentation. Publication and centralized consultation of analysis certificates (created on special Adiuto external systems), approval flows of quality system documents (procedures and forms). Data collection processes (CAPA, deviations) of the quality system. Management of data related to the training of Quality area personnel (ongoing project).
Complete management of the patient hospitalization process, from booking to discharge, which includes clinical and administrative management with related documentation. Active and passive management of the entire administrative cycle, including medical professional invoices, B2B (passive flow).
The system is used for the management of both GxP critical and non-GXP documents. Digitization of approval flows of procedures, forms, and production documentation (Master Batch Record). Digitization of the Change Control Management Process, Management of the quality manual and monographs, management of information related to human resources training in the implementation phase.
Digitization of document approval and process flows in different units belonging to Recipharm Italia, in compliance with EU-GMP Annex 11 and FDA-CFR 21 Part 11 regulations. Procedures and Forms, MBR, CAPA, Change Control, Deviations, Complaints. "Technical Customers Services" solution: in response to customer requests, the system allows activities to be assigned to the various corporate bodies involved. The activities, parallel or sequential, are mapped to the system, ensuring traceability until the request has been processed. ArtWorks Management Flow.
Complete management of the administrative cycle and transversal approval flows, signature collection with graphometric tablet for internal sales and for the collection of privacy, Expense Report Management, Digital Preservation according to regulations and B2B.
Management of the administrative cycle, with strong parameterization and customization of the active cycle in sending invoices, management of the passive cycle with authorization workflow and non-compliance management, parametric for the group's 15 companies. Integration with SAP and SAP VIM, regulatory compliance, and B2B.
Document management of orders, with classification and parameterization of permissions. Management of the supplier qualification process with CMS integration for supplier access during data entry phase and documents. Management of specialized courses for employee certifications.
Management of GxP quality processes, validated according to Annex 11 and CFR 21. Digitization of ”customer complaints" management, starting from reporting, investigation, and the opening of any corrective actions, with the involvement of pharmacovigilance, where necessary. Digital document signing flow. Involvement of external stakeholders (suppliers) in the supplier qualification process, with enterprise ERP SAP integrations.
Our White Papers
Consulting, methodology, and digital solutions for every critical business process
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Our institutional reports and Success Cases
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Adiuto adheres to the Mirandolese Biomedical District
Adiuto adheres to the portal of the most important Italian biomedical district and one of the main ones in the world.
The Biomedical District of Mirandola is considered the most important in the sector in Europe and third in the world; is a pole of companies specialized in the production of medical devices such as equipment and disposable products (so-called disposable) for therapeutic applications.
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Adiuto is member partner AFI 2023
Also this year Adiuto joins the AFI - Pharmaceutical Industry Association, confident of its innovative role in the digitization of critical processes in the world of Life Sciences. In particular, Adiuto, in support of Quality Assurance, enables the simplification and efficiency of Quality processes, in total safety and GMP compliance.
From 7 to 9 June 2023 Adiuto will be present at the 62nd AFI SYMPOSIUM 2022 "The Health Supply Chain: development engine for the country", at stand no. 55.
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Adiuto & CPA
Adiuto renews its membership of the Italian Association of Manufacturers of Active Ingredients and Intermediates for the generic drug market which represents the main companies in the Italian chemical-pharmaceutical industrial sector.
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Have you ever thought of managing supplier qualification in a digital and world-wide key?
Sharing, collaboration and involvement of suppliers in the main qualification processes with a clear reduction in wasted time and an improvement in perceived and real safety. Centralize the flow of information and involve the main stakeholders in the qualification processes with a click worldwide.
