The digital hub for inhaler testing data management
Bring methods, users, equipment information, inhaler testing data, reports and audit trails together within a controlled digital workflow.
Inhalytix®+ v2.0 strengthens equipment connectivity and expands the tools available for managing, analysing and reporting inhaler testing data, helping laboratories work with greater consistency, visibility and traceability.
sales@copleyscientific.co.uk
Bringing the inhaler testing workflow together
Inhaler testing data is rarely generated or managed in isolation. Methods, users, equipment configurations, analytical data, reports and review activities all contribute to the wider test record.
Inhalytix+ brings these elements into one controlled environment, helping laboratories manage inhaler testing workflows more consistently from method configuration through to analysis, review and reporting.
Bringing key workflow information together within one connected digital environment
Methods & Users
Controlled methods, roles and permissions
Create, control and version approved methods, manage authorised users, roles and permissions centrally, and make supported methods and user permissions available on compatible connected equipment.
Equipment & Set-up
Inventory, configurations and connected equipment
Manage equipment inventory and configurations centrally, connect compatible Copley equipment and bring supported equipment information into the wider test record.
Data & Analysis
Inhaler testing data, calculations, comparisons and trends
Import and manage inhaler testing data, calculate key APSD performance metrics automatically, and compare and analyse results.
Review & Reporting
Reports, workflow reviews and audit trails
Create and customise reports, manage structured review and approval, and maintain comprehensive audit trails.
Inhalytix®+ v2.0
The Digital Hub Inhaler Testing Data Management
A structured workflow for inhaler testing data
Inhalytix+ structures data management around a defined Prepare → Execute → Analyse workflow, helping laboratories manage test information consistently from method configuration through to final review and reporting.
1. Prepare
Define methods, equipment and reporting requirements
Create product-specific test methods and define the equipment configuration, APIs, stage groupings, reporting parameters and other relevant method settings.
Where supported, approved methods configured in Inhalytix+ can also be made available on connected Copley equipment, helping analysts work from controlled settings during testing.
2. Execute
Capture test data within the defined workflow
Enter inhaler testing data manually or import it from CSV or XLSX files. Data is associated with the relevant method and equipment configuration, helping maintain context throughout the analytical workflow.
3. Analyse
Calculate, compare and report results
Automatically calculate key APSD performance metrics, review graphical and tabulated results, compare tests and generate standard or customised reports.
Bring equipment information into the digital test record
Inhalytix+ provides a central Equipment Inventory for managing equipment information alongside methods, configurations and analytical records. Equipment can form part of the Inhalytix+ workflow in different ways depending on the product, model, firmware and connection type.
Connecting Copley Equipment with Inhalytix+
The Critical Flow Controller TPK 200iX demonstrates how direct connectivity can extend the Inhalytix+ workflow to critical flow control, bringing approved methods and user permissions into the equipment and returning supported operating information and reports to the wider digital test record.
Critical Flow Controller TPK 200iX
The Critical Flow Controller TPK 200iX supports direct connection with Inhalytix+, allowing approved methods and authorised user permissions managed in the software to be made available on the equipment. Supported operating information, equipment information and reports can then return to Inhalytix+ as part of the wider digital test record.
Explore the TPK 200iXDesigned for controlled laboratory workflows
Inhalytix+ is designed to support pharmaceutical laboratories working to major international pharmacopoeial and regulatory requirements, including Ph. Eur., USP, JP, ChP and relevant regulatory authorities. Alongside this, the software provides controls for managing electronic records, user access, review and traceability within the inhaler testing workflow.
Role-based user management
Manage authorised users, roles and permissions to support controlled access to methods, data and workflow functions.
Comprehensive audit trails
Capture key user actions, method changes, data edits, report review steps and system events, helping laboratories understand how records were created, changed, reviewed and approved.
Structured review and approval
Optional structured test sign-off supports formal review and approval before results are finalised, helping laboratories maintain defined review steps and appropriate user oversight.
GMP and 21 CFR Part 11 compliance
Inhalytix+ is designed to support GMP workflows and electronic record requirements in accordance with 21 CFR Part 11.
Built to evolve with your laboratory
Inhalytix+ provides a scalable digital hub that can evolve with laboratory requirements.
Laboratories can use the same controlled environment to manage methods, users, equipment information, APSD data, reports and audit trails, while extending connectivity to compatible Copley equipment as needs develop.
This enables laboratories to build connected capability over time while retaining a consistent digital foundation for managing inhaler testing data and workflows.
Explore Connected Inhaler Testing
Simple, all-inclusive subscription
Inhalytix+ is supplied as a three-year subscription, with licences available for teams of three users or more.
The subscription includes:
✔ Unlimited test run analyses
✔ Ongoing software and feature updates
✔ Built-in audit trails
✔ Customisable methods and reporting
✔ Comprehensive technical support
✔ Optional user training packages
Frequently Asked Questions (FAQs)
Inhalytix+ is specialist software for inhaler testing data management, analysis and reporting. It brings methods, equipment information, analytical data, reports, user management and audit trails together within a controlled digital workflow.
Inhalytix+ supports the management, analysis and reporting of APSD data for orally inhaled and nasal drug products.
Supported Copley equipment can exchange selected workflow information with Inhalytix+, depending on the product and connection type. Equipment can also be incorporated through QR identification or Equipment Inventory records.
No. Following initial licence activation, Inhalytix+ can operate without continuous internet access for day-to-day use. Internet access is required for licence renewal and software updates.
Talk to us about your inhaler testing data workflow
Whether you are looking to strengthen inhaler testing data management, improve equipment visibility or bring more of your Copley equipment into a connected workflow, our team can help you understand how Inhalytix+ could fit your laboratory requirements.
We have now released Inhalytix+ v2.0.0. To check that you are running the latest version of the software and benefiting from critical updates and bug fixes, please contact us via support@copleyscientific.co.uk.
In addition, we are now withdrawing support for the legacy product Inhalytix v2.3.0 and earlier. Please contact sales@copleyscientific.co.uk to discuss upgrading to the latest product. Note that Inhalytix v2.4.0 will continue to be supported.
