How ERP systems in the medical device industry reduce costs through real-time monitoring and process optimization.
Comprehensive security: Documentation & traceability
Integrated compliance: Features for regulated processes
More time: faster development through automated processes
Permission sets & role center
Define incident types & error codes
Create incidents from documents
Implement standardized CAPA processes
User-specific permission sets
Electronic signatures according to FDA 21 CFR Part 11
Traceability via audit trail
Field security by user role
Warehouse receiving & transfer
Consumption & actual reporting in production
UDI & serial number collection
Order picking with packaging structure
FEFO Strategies & Temperature Zones
Warehouse receiving & pre shipment inspection, storage
Map quarantine and inspection warehouses
Communication via EDI
Create manufacturing instructions
Batch inheritance & feature calculation
Consumption posting according to FIFO/FEFO
Integration with QA and technology
Our ERP for medical devices meets the industry's high demands, including strict compliance with MDR and FDA regulations. GMP-compliant processes, audit trails, and lot tracking ensure transparent operations. Specific requirements such as comprehensive documentation are addressed and supported by our validation consulting. Modules like formulation and production scheduling optimize workflows and ensure compliance with legal requirements.
Implementing a specialized ERP software for medical devices offers numerous benefits that cater to industry requirements. It ensures regulatory compliance and supports comprehensive documentation and traceability of production and quality control processes, which are crucial for audits and certifications. Additionally, the ERP solution optimizes production and resource planning through real-time data analysis, enabling efficient raw material use and preventing supply shortages. Transparency at every step of production minimizes errors and ensures product quality.
An ERP software aids in the production of medical devices by streamlining production scheduling, resource allocation, and inventory management. It reduces bottlenecks, ensures compliance with regulatory requirements, and facilitates the automation of production processes. This not only enhances efficiency but also improves traceability and quality assurance, which are critical in the manufacturing of medical devices.
The cost of implementing and maintaining an ERP software depends on factors such as the size of your medical device company, the chosen solution, the need for customization, and the required features. The expenses include initial costs for implementation and ongoing costs for updates, support, and training.
In addition to our comprehensive online help, various training videos are available to make it as easy as possible for users to get started with the new medical device software.
Together with Microsoft, we continuously deliver new updates to ensure our software remains cutting-edge and meets your exact requirements. Our goal is to provide solutions that not only adhere to current standards but are also forward-thinking and tailored to the specific needs of the medical device industry.
Cost control in the medical device industry – Beitrag öffnen
How ERP systems in the medical device industry reduce costs through real-time monitoring and process optimization.
ERP compliance in the medical device industry – Beitrag öffnen
For SMEs in the medical device sector, ERP compliance is mandatory. Here's how to implement the applicable regulations!
Validation-ready ERP for medical device companies – Beitrag öffnen
Learn how ERP systems meet GxP requirements with audit trails, documentation, and built-in compliance.
