HOME  COMPANY NEWS & EVENTS JOBS & CAREER  CONTACT   SEARCH 
PAS-X
Production Management
 
PAS-X Full Scope Packages

PAS-X CT
The best MES for Paperless Pharmaceutical Manufacturing and Packaging
 download brochure
(pdf, 1,8 MB)




 Computer Support during all Phases
 Ergonomic User Interface
 Quality by Design
 Equipment Integration




The PAS-X PHARMA Full Scope Package with its comprehensive array of functions covers the entire range of pharmaceutical manufacturing processes - from weighing and dispensing to the production of solids, semi-liquids, and liquids, through to filling and packaging of the products.

Computer Support during all Phases of the Manufacturing Process
Specification

PAS-X PHARMA's workflow engine offers you a comfortable way to describe the entire manufacturing and packaging processes, including recipes, material usage, specifications for quality assurance and documentation.

Workflow-Engine
 enlarge

You can use ERP orders as a basis for producing a detailed plan for the entire production and packaging sequences and workflows, including material availability.


Manufacturing Control

Specialized knowledge of best practices within pharmaceutical production has been used to develop functions which support the user in executing all shop floor manufacturing activities.
PAS-X PHARMA provides detailed instructions to guide the user securely through all manufacturing steps, beginning with the weighing of the input materials, to EBR-based equipment control and monitoring, through to the finished product. All the equipment items used in the manufacturing process are managed and released for use in production in the MES. Using advanced technologies such as barcodes or RFID, the material is identified, moved within the facility, and tracked. Warehouse functions are provided to support your storage logistics along the production line. All manufacturing steps are documented as electronic, and therefore paperless, FDA/GMP-compliant manufacturing reports.


Quality Assurance

PAS-X PHARMA supports all in-process actions required in the context of quality control and assurance. The "Review-by-Exception" strategy, for example, accelerates the batch release process. For the purpose of quality assurance, information on the operators' qualifications and training is also taken into account. CAPA functions do not only support manufacturing and packaging, but they also contribute toward constantly enhancing the quality of your products and processes.


Performance Increase

PAS-X PHARMA gives you a large selection of standard evaluation functions to help you increase your production performance. These functions create process transparency, and deliver facts and instruments which can be used to analyze and visualize your manufacturing processes on the basis of key performance indicators, subsequently optimizing the process in a systematic way.
Role-based, Ergonomic User Interface
The Electronic Batch Record provides an ergonomic user interface based on a "Right-First-Time" strategy, through all stages from weighing and manufacturing to filling and packaging of the products.
Quality by Design
Up-to-date manufacturing processes follow the Quality-by-Design (QbD) approach and use the potential of the "Design Space" as well as the "Control Strategy" required for flexible production. Supported by PAT-based multi-variant data models, this control strategy manages and runs the manufacturing process more efficiently and to a higher standard.
Equipment Integration
PAS-X PHARMA provides custom-built equipment interfaces for process equipment, especially for highly automated process engineering and manufacturing procedures, Integration covers the entire range, from OPC-based standard integration through to a supplier-specific DCS/SCADA system interface supporting the respective batch engines.
© Werum Software & Systems AG 2008 Privacy Statement Sitemap Print Page