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Streamline and automate quality management processes with fully validated life science QMS software. Get all QMS modules like document control, change management, training, CAPAs, and more in one solution.

QMS Modules by Industry

Document Control

Centralize and control documents and records with version control, e-signatures, and audit trails.

Training Management

Automate and manage training activities to support staff competence and maintain controlled training records.

Change Management

Streamline change control processes from request submission through review, approval, and implementation.

Design Control

Control and document design activities to manage risk and meet regulatory requirements.

Nonconformance Management

Capture and address nonconformances to correct issues and support timely resolution.

CAPA Management

Identify and address quality issues, implement corrective and preventive actions, and reduce recurrence risk.

Complaint Management

Log and manage customer complaints to support investigation, traceability, and reporting requirements.

Audit Management

Plan, conduct, and document audits to support inspection readiness and timely follow-up.

Risk Management

Identify, assess, and document risks to support mitigation and protect quality and compliance.

Equipment Management

Track and maintain equipment to support accuracy, availability, and compliance.

Supplier Management

Qualify and monitor suppliers to maintain oversight, traceability, and regulatory compliance.

Product Management

Manage product information and records to improve lifecycle visibility, traceability, and regulatory alignment.

Document Control

Centralize and control documents and records with version control, e-signatures, and audit trails.

Training Management

Automate and manage training activities to support staff competence and maintain controlled training records.

Change Management

Streamline change control processes from request submission through review, approval, and implementation.

Deviation Management

Record, investigate, and document deviations to support timely resolution and compliance.

CAPA Management

Identify and address quality issues, implement corrective and preventive actions, and reduce recurrence risk.

Complaint Management

Log and manage customer complaints to support investigation, traceability, and reporting requirements.

OOS Management

Capture, investigate, and document out-of-specification results to support timely resolution and compliance.

Audit Management

Plan, conduct, and document audits to support inspection readiness and timely follow-up.

Risk Management

Identify, assess, and document risks to support mitigation and protect quality and compliance.

Equipment Management

Track and maintain equipment to support accuracy, availability, and compliance.

Supplier Management

Qualify and monitor suppliers to maintain oversight, traceability, and regulatory compliance.

Electronic Batch Records

Digitally manage batch record documentation to improve traceability and support GMP compliance.

Document Control

Centralize and control documents and records with version control, e-signatures, and audit trails.

Training Management

Automate and manage training activities to support staff competence and maintain controlled training records.

Change Management

Streamline change control processes from request submission through review, approval, and implementation.

Deviation Management

Record, investigate, and document deviations to support timely resolution and compliance.

CAPA Management

Identify and address quality issues, implement corrective and preventive actions, and reduce recurrence risk.

Complaint Management

Log and manage customer complaints to support investigation, traceability, and reporting requirements.

OOS Management

Capture, investigate, and document out-of-specification results to support timely resolution and compliance.

Audit Management

Plan, conduct, and document audits to support inspection readiness and timely follow-up.

Risk Management

Identify, assess, and document risks to support mitigation and protect quality and compliance.

Equipment Management

Track and maintain equipment to support accuracy, availability, and compliance.

Supplier Management

Qualify and monitor suppliers to maintain oversight, traceability, and regulatory compliance.

Electronic Batch Records

Digitally manage batch record documentation to improve traceability and support GMP compliance.

Document Control

Centralize and control documents and records with version control, e-signatures, and audit trails.

Training Management

Automate and manage training activities to support staff competence and maintain controlled training records.

Change Management

Streamline change control processes from request submission through review, approval, and implementation.

Deviation Management

Record, investigate, and document deviations to support timely resolution and compliance.

CAPA Management

Identify and address quality issues, implement corrective and preventive actions, and reduce recurrence risk.

Complaint Management

Log and manage customer complaints to support investigation, traceability, and reporting requirements.

OOS Management

Capture, investigate, and document out-of-specification results to support timely resolution and compliance.

Audit Management

Plan, conduct, and document audits to support inspection readiness and timely follow-up.

Risk Management

Identify, assess, and document risks to support mitigation and protect quality and compliance.

Equipment Management

Track and maintain equipment to support accuracy, availability, and compliance.

Supplier Management

Qualify and monitor suppliers to maintain oversight, traceability, and regulatory compliance.

Electronic Batch Records

Digitally manage batch record documentation to improve traceability and support GMP compliance.

Document Control

Centralize and control documents and records with version control, e-signatures, and audit trails.

Training Management

Automate and manage training activities to support staff competence and maintain controlled training records.

Change Management

Streamline change control processes from request submission through review, approval, and implementation.

Deviation Management

Record, investigate, and document deviations to support timely resolution and compliance.

CAPA Management

Identify and address quality issues, implement corrective and preventive actions, and reduce recurrence risk.

Complaint Management

Log and manage customer complaints to support investigation, traceability, and reporting requirements.

Audit Management

Plan, conduct, and document audits to support inspection readiness and timely follow-up.

Risk Management

Identify, assess, and document risks to support mitigation and protect quality and compliance.

Equipment Management

Track and maintain equipment to support accuracy, availability, and compliance.

Supplier Management

Qualify and monitor suppliers to maintain oversight, traceability, and regulatory compliance.

Electronic Batch Records

Digitally manage batch record documentation to improve traceability and support GMP compliance.

Product Management

Manage product information and records to improve lifecycle visibility, traceability, and regulatory alignment.

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