Electronic Signature Software
Sign and send any document with Electronic Signatures through an automated workflow from practically anywhere in the world, at any time.
FDA 21 CFR Part 11 compliant digital signature
SimplerQMS complies with FDA 21 CFR Part 11 and the GxP Guidelines. This means that you can manage any quality record digitally and avoid using paper.
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.
Perform 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 allow for a seamless and fully digitized process – supporting both internal and external users.
Looking for more modules?
Regardless of the stage of your Life Science organization, our integrated software modules cover all your needs.
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 management 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.
Manage your equipment calibration schedule and automatically assigns tasks before due dates.
Simplify your issue management workflows by automating tedious tasks.
Plan and organize all your product management activities and integrate them with other processes.
Automate your audit-related activities and ensure better audit preparedness.
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.
Standardize your documentation processes and boost employee productivity with effective document forms.
Streamline the investigation, documentation, and resolution of all your deviations.
Electronic Batch Records
Digitize and automate your batch record processes to ensure regulatory compliance.
Identify, evaluate, analyze and manage nonconformances more efficiently.
Trusted by companies around the world
Ready to learn more?
To learn how you can make the most of SimplerQMS, request a free, personalized demo presentation.