Medical device manufacturing and trading company seeks quality management

We are a manufacturing and trading company for medical devices and are looking for a quality management system for medical devices, including risk management, taking into account vigilance and PMS.

The software should meet the following requirements:

• Risk management
• Quality management
• Standards management
• Create medical device files
• Market observation using PMS (post-market surveillance) – monitoring of medical devices after they have been placed on the market
• e.g., proactively generate information through targeted surveys and analyses
• Environmental management
• Occupational safety
• Document management
• Knowledge database to which all employees should have access (company knowledge, background information, importing standards updates)
• Consideration of medical device law (legal changes)

5-10 software workstations are required. Work is carried out in an MS Windows environment.