Electronic Signature Software

Sign and send any document with Electronic Signatures through an automated workflow from practically anywhere in the world, at any time.

SimplerQMS Electronic Signature Software

21 CFR Part 11 compliant eSignature

SimplerQMS complies with 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.

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.

Training Management Module Icon

Training Management

Save time with automated training activities, learning overview, reminders, and generation of training certificates.

CAPA Management Module Icon

CAPA Management

Identify, uncover, resolve, and report all the preventative actions and corrective actions (CAPAs) seamlessly.

Complaint Management Module Icon

Complaint Management

Reduce the associated risks and resolve issues quickly by optimizing complaint, nonconformance, and deviation processes.

Change Management Module Icon

Change Management

Recognize and manage all changes accordingly to ensure compliance and structure within your organization’s QMS.

Design Control Module Module Icon

Design Control

Manage all the necessary processes related to product design and meet Design Control requirements with ease.

Document Management Module Icon

Document Control

Automate and standardize your document control activities with ease.

Equipment Management Module Icon

Equipment Management

Have an overview of your equipment and handle tasks in an organized manner.

Electronic Signature Module Icon

Electronic Signatures

Sign and send the necessary documents for authoring, review, approval, from anywhere in the world, at any time.

Product Management Module Icon

Product Management

Plan and organize all your product management activities and integrate them with other processes.

Post-Market Surveillance Module Icon

Post-Market Surveillance

Remain in compliance and monitor the safety and the performance of the product in the market.

Risk Management Module Icon

Risk Management

Consolidate risk and handle your risk management file in a well-organized and structured manner.

Supplier Management Module Icon

Supplier Management

Simplify supplier-related activities and handle your supplier documentation following the standards.

Trusted by companies around the world