Supplier Management Software
Achieve efficiency and compliance in your supplier management activities.
Streamline your supplier process
Keeping track of your supplier documentation in a manual system is error-prone on time-consuming. With SimplerQMS you can digitize and automate your process such as selecting, evaluating, qualifying, and monitoring your suppliers.
Organize supplier management tasks
Schedule reoccurring supplier reviews and receive notifications about pending tasks seamlessly. Maintain a list of approved suppliers and use forms & templates to create records such as contracts, surveys, evaluations, certificates, and incoming inspections.
Find supplier documentation quickly
Search for a supplier name, a sourced component, or a document and quickly find the information you are looking for. Click the supplier dashboard and get an overview of all records which are related to each supplier. You can also drag and drop external documents like certificates to your Supplier File to easily retrieve them when needed.
Ensure compliant supplier processes
Use SimplerQMS to enforce supplier processes that are compliant with regulations such as ISO13485:2016, 21 CFR Part 820, and ICH Q9 and Q10. Automate continuous monitoring of suppliers and use our audit-ready dashboards to quickly show the relevant evidence to inspectors and auditors. Plan supplier audits and link suppliers, supplier findings, and CAPA’s to seamlessly overview your documentation.
The SimplerQMS modules cover all your processes
No matter if your life science organization is a start-up or a later stage company, our integrated modules cover your needs. All modules are included in the SimplerQMS Subscription and you get to choose when they should be implemented.
Save time with automated training activities, learning overview, reminders, and generation of training certificates.
Identify, uncover, resolve, and report all the preventative actions and corrective actions (CAPAs) seamlessly.
Reduce the associated risks and resolve issues quickly by optimizing complaint, nonconformance, and deviation processes.
Recognize and manage all changes accordingly to ensure compliance and structure within your organization’s QMS.
Manage all the necessary processes related to product design and meet Design Control requirements with ease.
Automate and standardize your document control activities with ease.
Have an overview of your equipment and handle tasks in an organized manner.
Sign and send the necessary documents for authoring, review, approval, from anywhere in the world, at any time.
Plan and organize all your product management activities and integrate them with other processes.
Remain in compliance and monitor the safety and the performance of the product in the market.
Consolidate risk and handle your risk management file in a well-organized and structured manner.
Simplify supplier-related activities and handle your supplier documentation following the standards.