Electronic Signature Software
Sign and send any document with Electronic Signatures through an automated workflow from practically anywhere in the world, at any time.
Sign external documents
External documents can be imported and signed in SimplerQMS. Documents are sent through an automated workflow the participants will receive notifications every time they have to take action.
Do documentation tasks on the go
Sign and send documents and files from any device, at any time and accelerate your current document management workflows. SimplerQMS can be used on any device through the Windows Application, Web Application, or Mobile Applications (iOS and Android).
Use pre-approved form package
Standardize your documentation processes and save time with our pre-approved forms and Standard Operating Procedures (SOPs). It is up to you if you decide to adopt procedures, forms, and instructions from our QMS form package or if you wish to migrate any existing procedures, forms, etc. to SimplerQMS.
See our eSignatures and Workflow in Action
This short video demonstrates how SimplerQMS enables you to sign any record with our Part 11 Compliant eSignatures. Automated workflows and notifications allows for a seamless and fully digitized process – supporting both internal and external users.
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.