MoPS is a digital platform for company-wide collaboration, communication and for the management of laboratory environments. MoPS improves workflows, avoids redundancies, facilitates communication and manages your data. This creates additional value and gives your company a significant advantage in the market.

MoPS manages and stores analytical methods and SOPs. You can create and validate your methods and upload method related documents to the platform, making them accessible anytime, anywhere and shareable with colleagues. You can update advancements in real-time and collaborate with colleagues for a seamless and targeted workflow.

Digital Workplace

• Individual customer solutions by modular design

• User Experience Design (UX design) for improved acceptance and usage rates

• Web-based and responsive, accessible from anywhere with any device

• Branded in your organizations' corporate identity

• Open system architecture for seamless integration of existing software solutions

• Direct data transfer between lab devices and users

Data Storage & Administration

• Integrated storage of all document types

• Company-wide knowledge base and archive

• Folder and file management including access protection and rights management

• Advanced search functions

• Simultaneous editing of documents by multiple users with version control

Social Interaction

• Calendars (group and individual)

• Appointment management

• News

• Newsletter

• Discussions and forums

• Contact management

• Resources planning and management

Method Management

• Complete transparency for method development, validation and approval

• Complete workflow solution

• Customer defined templates preventing manual data entry errors

• Multi-level user roles and rights management

• Audit trails and tracking features

• Audit-compliant reports

• Automatic report creation

• Internal drag and drop support

• Simultaneous editing of documents by multiple users with version control

Validation

• Step-by-step validation assistant for any method type

• Well-structured work processes and flexible, customer defined templates

• Multi-level user roles and rights management

• Interface connecting to external systems or software

• Direct data transfer between lab devices and users

• Automated report creation

• Audit trails and tracking features

• Audit-compliant reports

• 21 CFR 11 compliance support toolset

• Simple documentation review and reporting

• Reports meet all GxP, FDA and ISO guidelines

• Closed communication channel for each validation process

• Simultaneous editing of documents by multiple users with version control

SOP-Generator

• Automated creation of audit-compliant SOPs

• Audit trails and tracking features

• Internal drag and drop support

• Simultaneous editing of documents by multiple users with version control

• Closed communication channel for each SOP creation

• SOPs meet all GxP, FDA and ISO guidelines

• 21 CFR 11 compliance support toolset