Agile product lifecycle management
A reliable module to fully monitor your product's journey, from design to post production
Enable efficient audits with Power Apps
- Dedicated to auditors or inspectors working on the field, production lines or visiting clients, suppliers, etc., this app can be used with any mobile device, anywhere, even without an internet connection.
- Maximize auditor’s experience for any type of audit, like internal, supplier, product, process or system audits and inspections, with Audits Power Apps.
Enrich audits with pictures and voice recordings
- When starting an audit, related questions are displayed and auditors can easily evaluate compliance with color flags. Pictures and voice recording can be appended to any question during the audit. All content is automatically synched in the BPA software, where follow-up actions will be handled.
- Built on Power Apps, the app brings the needed security and connectivity with Microsoft 365 technologies.
An all-in-one platform
- Our medical quality and compliance software brings features to manage the whole product lifecycle from the design input phase to post production, including modules for preliminary hazard analysis, failure mode and effect analysis, and change management.
Robust automation
- Prebuilt workflows help to automatically provision technical files for the different product versions, based on your document and form templates.
FMEA risks automatically provisioned
- FMEA risks are automatically provisioned from previous product versions to new versions.
Agile eQMS modules for all your requirements
Document Control
Change Management
Non-Conformances Management
Audit Management
Process Management
Training Management
CAPA Actions
Equipment Management
Risk Management
Supplier Management
Health & Safety
Information Security
Environmental Aspects
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See firsthand what BPA Solutions has to offer
“We were able to successfully integrate our 1200 quality documents into an electronic, fully managed system with versioning control and electronic signatures, which is something that we have to implement for our regulatory requirements.....”