Quality Management Systems (QMS) for Pathology

Surity specialises in supplying Quality Management System solutions to Australian Health organisations.

Surity’s Quality Management System (QMS) solution provides an organisation-wide secure document lifecycle management system with standard framework for regulated documents and other related modules.

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► Quality Management System (QMS) Solutions

Success Stories

Solutions for Pathology Find out how we can help your business with document and imaging workflow management solutions engineered specifically for pathology laboratories.

Information Management Solutions
Software and professional services to solve your information management issues and return substantial benefits.

Integration Solutions
Technology and professional services to rapidly integrate your legacy applications to provide maximum value and flexibility.

Surity's Implementation Approach
Find out how our carefully engineered implementation approach benefits your project.

Surity’s QMS Solution Benefits

Provides a powerful document management and business workflow solution.
Easily configurable to capture, manage and report on all essential information.
Ensures compatibility with AS4633.
Ensures that all legal requirements are met.
Each unit/hospital/lab can have separate repository and/or server with components shareable and searchable by all those with security rights.
Ability to measure and monitor performance, and benchmark due to the same platform, features and functionality, such as Audit trails, and security.
Ability to leverage off work done in other labs.
Allows for the incorporation of “best practices”.
Autonomy and independence possible yet conforming to standards.
Reduces paperwork and increases staff participation.
Facilitates smooth and effective communication with staff members and stakeholders.
Provides a central system to facilitate continual process improvement.
Powerful reporting.

Surity's QMS Solution Features

Full Document Lifecyle Management and Control

Author, Review, Authorisation, Publishing, Dissemination, Destruction
Electronic Signatures
Modular Functionality
Non-Conformance, Complaints, Hazards register
OH&S and Risk Management
Management of Internal Audits
Equipment Register
SOP Training Program

Compliance and Accreditation

Compliance to AS4633 Standards
Compliance with 21 CFR Part 11
Ease of internal audit and production of reports for all compliance requirements.

Collaborative environment

Able to share documents/information/processes/best practices yet keep own set of information based on access/security.
Common processes with variations based on Hospital/lab requirements.
Able to work on same projects across groups, and even bring in external groups.
Non-Conformance, Complaints, Hazards register
OH&S and Risk Management
Management of Internal Audits
SOP Training Program