Quality Management Modules
No matter if you are a start-up or a later-stage company, in a Pharmaceutical, Medical Device, or other Life Science industry, our integrated QMS modules cover all your needs.
TRUSTED BY
QMS Modules by Industry
Document Control
Generate, approve, and control quality and regulatory documentation from a central location.
Training Management
Design and implement employee training plans, track progress, and assess effectiveness.
Change Control
Implement changes in your QMS effectively without compromising on structure or compliance.
Design Control
Manage all the necessary processes related to product design and meet design control requirements.
Nonconformances
Record, evaluate, analyze, and manage nonconformances throughout your organization.
CAPA Management
Efficiently identify, investigate, and implement corrective and preventive actions.
Complaints Management
Efficiently record, track, manage, and resolve customer complaints in a timely manner.
Audit Management
Simplify audit processes by effectively planning, executing, and tracking internal and external audits.
Risk Management
Execute effective risk assessments and mitigation strategies to safeguard your operations and compliance.
Equipment Management
Easily control and manage equipment, equipment maintenance, and calibration tasks.
Supplier Management
Simplify supplier-related activities and handle your supplier documentation following the requirements.
Product Management
Manage and trace all product-related documentation and changes for comprehensive oversight.
Document Control
Generate, approve, and control quality and regulatory documentation from a central location.
Training Management
Design and implement employee training plans, track progress, and assess effectiveness.
Change Control
Implement changes in your QMS effectively without compromising on structure or compliance.
Deviation Management
Streamline the evaluation, documentation, and resolution of all deviations.
CAPA Management
Efficiently identify, investigate, and implement corrective and preventive actions.
Complaints Management
Efficiently record, track, manage, and resolve customer complaints in a timely manner.
Out-of-Specifications
Manage out-of-specification (OOS) results effectively to maintain product quality and integrity.
Audit Management
Simplify audit processes by effectively planning, executing, and tracking internal and external audits.
Risk Management
Execute effective risk assessments and mitigation strategies to safeguard your operations and compliance.
Equipment Management
Easily control and manage equipment, equipment maintenance, and calibration tasks.
Supplier Management
Simplify supplier-related activities and handle your supplier documentation following the requirements.
Electronic Batch Records
Manage batch records electronically to expedite production and ensure regulatory adherence.
Document Control
Generate, approve, and control quality and regulatory documentation from a central location.
Training Management
Design and implement employee training plans, track progress, and assess effectiveness.
Change Control
Implement changes in your QMS effectively without compromising on structure or compliance.
Deviation Management
Streamline the evaluation, documentation, and resolution of all deviations.
CAPA Management
Efficiently identify, investigate, and implement corrective and preventive actions.
Complaints Management
Efficiently record, track, manage, and resolve customer complaints in a timely manner.
Out-of-Specifications
Manage out-of-specification (OOS) results effectively to maintain product quality and integrity.
Audit Management
Simplify audit processes by effectively planning, executing, and tracking internal and external audits.
Risk Management
Execute effective risk assessments and mitigation strategies to safeguard your operations and compliance.
Equipment Management
Easily control and manage equipment, equipment maintenance, and calibration tasks.
Supplier Management
Simplify supplier-related activities and handle your supplier documentation following the requirements.
Electronic Batch Records
Manage batch records electronically to expedite production and ensure regulatory adherence.
Document Control
Generate, approve, and control quality and regulatory documentation from a central location.
Training Management
Design and implement employee training plans, track progress, and assess effectiveness.
Change Control
Implement changes in your QMS effectively without compromising on structure or compliance.
Deviation Management
Streamline the evaluation, documentation, and resolution of all deviations.
CAPA Management
Efficiently identify, investigate, and implement corrective and preventive actions.
Complaints Management
Efficiently record, track, manage, and resolve customer complaints in a timely manner.
Audit Management
Simplify audit processes by effectively planning, executing, and tracking internal and external audits.
Risk Management
Execute effective risk assessments and mitigation strategies to safeguard your operations and compliance.
Equipment Management
Easily control and manage equipment, equipment maintenance, and calibration tasks.
Supplier Management
Simplify supplier-related activities and handle your supplier documentation following the requirements.
Electronic Batch Records
Manage batch records electronically to expedite production and ensure regulatory adherence.
Customer Management
Maintain a list of customers, distributors, and contacts, linked to relevant products and documents.
Document Control
Generate, approve, and control quality and regulatory documentation from a central location.
Training Management
Design and implement employee training plans, track progress, and assess effectiveness.
Change Control
Implement changes in your QMS effectively without compromising on structure or compliance.
Deviation Management
Streamline the evaluation, documentation, and resolution of all deviations.
CAPA Management
Efficiently identify, investigate, and implement corrective and preventive actions.
Complaints Management
Efficiently record, track, manage, and resolve customer complaints in a timely manner.
Audit Management
Simplify audit processes by effectively planning, executing, and tracking internal and external audits.
Risk Management
Execute effective risk assessments and mitigation strategies to safeguard your operations and compliance.
Equipment Management
Easily control and manage equipment, equipment maintenance, and calibration tasks.
Supplier Management
Simplify supplier-related activities and handle your supplier documentation following the requirements.
Electronic Batch Records
Manage batch records electronically to expedite production and ensure regulatory adherence.
Product Management
Manage and trace all product-related documentation and changes for comprehensive oversight.
Solutions to Your Quality Management Challenges
Efficiency and Productivity
Streamline workflows and enhance productivity with visual workflows, task management, and automated reminders.
SimplerQMS facilitates efficient file sharing and project management, reducing manual efforts.
Related Features
Visual Workflows
Visualize workflows for a clear understanding of document processing and related steps.
Actions & Tasks
Assign and manage actions with a range of options, linking them to documents or other items.
Reminders
Implement event-triggered reminders, ensuring timely completion of tasks and assignments.
File Storage & Sharing
Store, organize, and share any file of any size without using Sharepoint, Dropbox, OneDrive etc.
Project Management
Enhance project management with organized document linking and process hierarchies.
Approver, Reviewer Groups
Efficiently distribute tasks with options to assign review and approval duties to groups or individuals.
Compliance and Control
Simplify compliance with life science-specific QMS templates, the FDA 21 CFR Part 11 compliant electronic signatures, and audit trails.
SimplerQMS supports controlled printing and regulatory requirements management, ensuring adherence to applicable regulatory requirements.
Related Features
Life Science QMS Templates
Simplify quality management with compliant QMS templates for manuals, procedures, forms, and instructions.
User Access Management
Ensure secure access for both internal and external users while maintaining system integrity.
Electronic Signatures
Implement a paperless signing process with electronic signatures, providing authenticity and integrity.
System Audit Trail
Maintain a detailed audit trail of all system changes in compliance with 21 CFR Part 11.
Controlled Printing
Control and monitor document printing to ensure compliance with regulatory requirements.
Reg. Standard Management
Manage and monitor adherence to regulatory requirements, and quickly access relevant documentation.
Reporting and Information Management
Make informed decisions with our KPI reporting and information management capabilities.
SimplerQMS offers tools for tracking quality KPIs, efficient content search and indexing, and easy export of data, facilitating a data-driven approach to quality management.
Related Features
Quality KPIs
Monitor the health of your quality systems with quality Key Performance Indicator (KPI) reports.
Content Search & Indexing
Find what you need swiftly with Google-like search capabilities, navigating through all content.
Export Data & Content
Export documents and system metadata easily for analysis or integration with external tools.
Customization and Integration
Tailor your quality management experience with our customizable and integrative QMS software.
SimplerQMS allows for the creation of custom fields, forms, and templates for data capture, and offers API & system integrations for data synchronization with external tools.
Related Features
Custom Fields
Configure custom fields, such as dropdowns, text, number, and date fields, to tailor data capture.
Template Management
Streamline the creation and utilization of standardized forms and templates across your organization.
API / System Integrations
Facilitate efficient data flow between your QMS and external systems with integrations.
Comprehensive QMS Software That Grows With You
Starter
For small teams looking to get started with streamlining their QMS processes.
Up to 5-10 users
Starts at $1,150/month
ALL-INCLUSIVE SUBSCRIPTION
All eQMS modules
Full system implementation
Fully validated system
Continuous re-validation
Dedicated project manager
User training
Cloud-hosting
Integrations to other enterprise solutions
Team & Enterprise
Everything you need for an eQMS implementation.
More than 10 users
Request a demo for a price estimate
ALL-INCLUSIVE SUBSCRIPTION
All eQMS modules
Full system implementation
Fully validated system
Continuous re-validation
Dedicated project manager
User training
Cloud-hosting
Integrations to other enterprise solutions
For more information on SimplerQMS and licenses, please see our pricing page.
Support That Always Has Your Back
Online Training Sessions
Receive comprehensive training, and ensure you and your team are proficient in using the software.
24/7 Customer Support
Our expert team is always available to promptly address your queries and provide assistance.
Knowledge Base
Access our knowledge base for articles, and guides complementing our dedicated customer support.
Have a question for our sales team? Give us a call and we will walk you through it.
+1 888-830-9807
See What Our Customers Have to Say
“Spending most of my day using SimplerQMS, I would say I am very pleased with the ease of use.”
Dorthe W.
QA/RA Manager, Cortex Technology
“SimplerQMS gave us excellent pricing, customer support for understanding how to use their system and set up our QMS, and is easy to use.”
Subba S.
Chief Technology Officer, CollaMedix
“Easy to work with. Intuitive. Rather easy to setup. Very good customer support. Good quality to price ratio.”
Jean Claude M.
Head of Hardware and Software Development, hemotune
See SimplerQMS in Action
To see SimplerQMS in action and learn how you can make the most of it, request a personalized demo presentation.
