Teams Medical Software

Medical Compliance Software on Teams & Office 365 – Introduction Video

Medical Compliance Software on Microsoft Teams and Office 365.

BPAMedical365 is a disruptive cloud software for quality and compliance, designed for any regulated industry, ready to be installed in your secure Microsoft Teams and Office 365 environment. The app is modern – runs on any device – it’s flexible to adapt to your needs – and innovative – leveraging your Microsoft 365 tools.

The app includes prebuilt integrated modules to cover ISO 13485, FDA and Medical Device regulations.

Use the app on any device, like a phone or a tablet, to access documents, view eSignatures, navigate in the QMS, view nonconformities, log an incident using intelligent conditional forms, and search the whole QMS portal.

With Teams, you have a single entry point to access your QMS, including discussions to instantly interact with team members, approvals, and video conferencing. This will boost efficiency !

The app is not like a traditional quality tool, it’s a collaborative workspace for the whole company, dedicated to continual improvement, and including all SharePoint capabilities.

eSignatures ensure only authorized users sign their piece of work, like approving a compliance document, or investigating a nonconformity.

BPA has developed prebuilt Power Automate workflows for each software module, ready to be imported in your tenant.

Ready-for-use Power BI reports bring consolidated data to managers for quick decision making.

We have developed generic Power Apps to plug and play with BPAMedical365 for easy incident registration by taking photos and simplified auditing even while offline.

Go a step further, meet your industry 4.0 objectives, comply with good practices in regulated industries, and reach instant quality improvement with BPAMedical365, Teams and Microsoft technologies.

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Product Videos

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Testimonials

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Office 365 eSignature Video

eSignature for Everyone, on Any Device, with SharePoint and Office 365

Modern eSignature component to be used in your Office 365 environment.

For regulated industries, electronic signature is required for a QMS software to be compliant with FDA and ISO 13485 regulations. For any organization, eSignature makes sure only authorized users approve documents or records.

BPA has developed an innovative eSignature component to be used with our apps on any device, directly within SharePoint and Teams.

eSignatures can be used internally to sign compliance documents, technical files, investigate incidents, or replace any paper signature. It can also be used with external suppliers to sign nonconformities or any other usage.

In this video we demonstrate how easy you can sign a compliance document, and a nonconformity form with multi factor authentication.

eSignatures can be added on any form by a simple drag and drop and protect document content or selected attributes.

BPA eSignature component gives the extra security needed when approving items in compliance with medical regulations. It makes SharePoint a more secure platform when signing documents or records, with no need to manage complex item-level permissions. It’s perfectly integrated with Microsoft 365 and multi factor authentication.

BPA eSignature is available at no additional cost with our modern Quality-Medical-CRM apps on Microsoft 365.

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How BPA’s Software Meets IATF 16949 Requirements for Automotive Industries

IATF 16949:2016 is an independent QMS standard, dedicated to the automotive sector, that is fully aligned with the requirements of ISO 9001:2015.

IATF 16949 includes specific requirements and core tools from the automotive industry, like:

  • Advanced Product Quality Planning (APQP)
  • Failure Mode and Effects Analysis (FMEA)

APQP ensures the voice of the customer is clearly understood, translated into requirements, technical specifications and special characteristics. APQP is typically used when introducing a new product, process or qualifying, evaluating new suppliers. From design to production, the APQP tracking sheet makes sure you go through each step and meet all needed requirements.

APQP

Screen Capture of BPA Quality & Risk Management, APQP example.

BPA’s software brings simple collaborative tools to track APQP projects with their milestones, related question sets, compliance and documents. Workflow rules ensure the right persons are automatically alerted to plan actions or mitigate risks.

Failure Mode and Effects Analysis (FMEA) is a structured approach to discovering potential failures that may exist within the design of a product or process. Discovering a failure early in product development using FMEA improves the product design and lowers cost. Important FMEA steps are to identify failure modes and assess their severity, identify causes and probability of occurrence, set up preventive process controls (detection). As a result, FMEA highlights Risk Priority Numbers (RPN) for each identified failure mode. Actions will be taken to mitigate high risks.

FMEA

Screen Capture of BPA Quality & Risk Management, FMEA example.

FMEA is a collaborative process that can be easily tracked with BPA’s software, replacing inefficient spreadsheets.

BPA Quality & Risk Management is leveraged by the benefits of Microsoft Office 365 technologies.

Ask for a free discovery access now.

BPA xRM platform for public sector and government

“This SharePoint xRM template has helped to streamline our communication within the department as well as with outside entities such as the Governor’s Office or Legislature.”

Vaughn Hammond – State of Alaska – US

Do you want to ensure accessibility and transparency of information, reduce workloads, improve data quality and stakeholder satisfaction…? Lire la suite