By embedding GAMP methodologies from the ground up, XFP software offers robust, pre-validated, Life Sciences-specific solutions to effectively translate manufacturing processes into operational excellence.

Over 120 pharmaceutical plants worldwide have improved visibility and efficiency in their entire facilities using XFP software. Fully ISA 95-compliant, XFP software can be deployed globally or at the plant level.

XFP Software integrates seamlessly with SIMATIC IT complementary solutions, ERP and PLM systems.

Main Benefits

XFP Weighing & Dispensing

Weighing is one of the most critical steps in pharmaceutical manufacturing: if the weighing is inaccurate, the batch is lost. With XFP Weighing & Dispensing, you get it right, first time, every time.

XFP Weighing & Dispensing ensures accurate and consistent weighing of all material types. Displaying on-screen instructions through intuitive user interfaces, XFP Weighing & Dispensing guarantees a total conformance to cGMP procedures.

The extensive use of barcode technology and integrated controls eliminates errors and reduces cycle times dramatically.

Regulatory reviews and product releases are made easier and faster thanks to the recording and tracking of all actions performed, with a detailed weighing report.

XFP MBR

XFP MBR (Master Batch Record) is an advanced workflow tool that helps optimize processes across multiple facilities. XFP MBR enables users to design Master Batch Records and graphically model, maintain and optimize processes, without any IT skills required. XFP MBR enables point & click modeling, reusable process objects and offers standardized work instructions.

The ISA88-compliant process hierarchy simplifies and accelerates process modeling, updates and validation. With the version control feature, it is easy to forecast the impact of process changes, thus greatly optimizing process maintenance and creation. A testing environment allows for process simulation before production.

XFP Directed Manufacturing

XFP automates and streamlines the manufacturing processes while ensuring full compliance with FDA regulations.

Manufacturing instructions are automatically displayed to the right user through an easy-to-use and intuitive interface.

The XFP directed manufacturing module simplifies data collection, performing automatic controls and minimizing errors.

The process execution is efficient and totally secure. Process data are gathered in a central repository, where they are available for reporting and analysis. This provides extended visibility and enables continuous process improvement.

Seamlessly integrated with third party systems, XFP provides full paperless manufacturing solutions.

XFP eBR

XFP eBR automates and streamlines the manufacturing processes while ensuring full compliance with FDA regulations.

Manufacturing instructions are automatically displayed to the right user through an easy-to-use and intuitive interface. The process execution is efficient and totally secure. Process data are gathered in a central repository, where they are available for review, reporting and analysis.

Through configurable signature paths, XFP eBR ensures and records compliant review by qualified personnel. Real-time visibility of batch review tasks allows the signatories to organize and manage their tasks with greater efficiency. They can instantly view exceptions and associated solutions, simplifying the validation process. 

XFP Packaging

XFP provides an FDA- and cGMP-compliant packaging environment, helping Life Sciences companies to deliver quality products on time.

By seamlessly integrating with both the packaging lines and the ERP, XFP can manage, control and track all primary and secondary packaging operations.

By using XFP packaging capabilities, pharmaceutical manufacturers are able to maintain a continuous supply of items during the packaging process. They can reduce line set-up time while streamlining and securing packaging operations.

This translates into increased performance of the overall packaging process.