Specification documents, validation procedures, and administration — ELO lets you automate and maintain an audit trail of your processes.
Companies in the pharmaceutical and medical technology industry are subject to a wide range of regulations: industry standards and statutory requirements have a major impact on quality management workflows and documentation. At the same time, companies need to streamline processes and keep costs to a minimum.
Our ELO ECM Suite helps you to meet these requirements:
- File and manage relevant documents, such as SOPs, work instructions or forms in line with processes
- Optimized training management verifies instruction in validated documents
- Authenticate the validity of documents using watermarks
- Version control ensures that the life cycle of important documents is fully traceable
- Integration of third-party systems, e.g. ERP systems (SAP, Microsoft Dynamics NAV, abas ERP etc.), merchandise management systems (including WinLine), and in-house solutions
- Automated invoice processing and e-mail archiving
All processes are integrated in ELO and can of course be tailored to your needs.
Benefits
Compliance
Sensitive data is stored in compliance with statutory retention periods and other requirements.
Standardized yet individual solutions and more than 10 years' validation experience in ELO and SAP, including solutions for life sciences — that is what sets us apart as a business partner.
Alexander Korn, managing director, quaris GmbH
