eQMS for the Medical Device Industry
Get eSignatures and Automated Workflows
in a Pre-Validated eQMS.
The SimplerQMS modules cover all your processes
No matter if your Medical Device organization is a start-up or a later stage company, our integrated modules cover your needs. All of the modules are included in the SimplerQMS Subscription.
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.
Featured Case Study
From Paper to Digital Workflows in 1 Month
Reapplix is a regenerative medicine company that helps people who suffer from hard to heal diabetic foot ulcers, which may result in amputation. The company is in the initial commercialization phase in the US and selected European markets and was looking for a way to get rid of inefficient paper-based documentation and processes.