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Qualio

Name: Qualio
Rating: 4.5 (2 reviews)

By Qualio

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Highlights : About Qualio

Action management

Activity tracking

Audit trail

Automatic reminders

Change management

Collaborative review

Corrective actions

Document review

HIPAA compliance

About Qualio

Qualio is the easiest way for businesses in Healthcare & Life Sciences to manage Quality and Compliance. Qualio automates the painful paperwork and processes required by regulators like the FDA for 2x faster accreditation and approval. It helps you work 5x faster than paper or traditional solutions to manage Document Control, Training, NCRs, CAPAs, Audits, Suppliers, Complaints and more. Define workflows for approval and review. Create records with automated numbering and easy linking of related content. Capture approvals with digital signature and automatically notify users of approved documents. You can use Qualio to manage training with automated notifications, reminders and training lists. Ensure compliance with any regulatory body and generate comprehensive audit trails to further meet compliance. All your data is securely stored and backed-up through Qualio. Using Qualio, you can reduce costs through streamlining time consuming workflows by 5x and lowering risk through automating the recording of key compliance information. In addition, Qualio's simple and powerful reporting makes it easy to see what's happening in real-time. Utilize Qualio's partner network of experts to work with you through the software and provide you with the key knowledge you need. Qualio provides an intuitive interface and live support so you can get started immediately.

Specifications

Business Size

Mid-Market

Language Support

English

Platforms

Product Details

Benefits

Designed for Medical Devices, Biotech, Pharma, Digital health and CxOs (Manufacturing, Testing Laboratories, Research Orgs)

Maintain 100% compliance and audit readiness at all times.

Set up automatic email notifications to reviewers and approvers.

Real-time parallel approval process. All reviewers can view the same document and previous versions can be compared against each other.

Easily collaborate. You can add comments and mark documents as reviewed to immediately notify the author.

Send automatic training notifications via email to your team at any time.

Stay compliant with with real-time and detailed insights into documents, people and actions. Monitor content sent for review, approval and training. Track change controls in progress and completed training.

Everything is fully customizable. Create your own templates for documents, forms and records. You can even specify document numbering and approval processes.

Designed to help you comply with important quality standards Including: Quality management systems (ISO 9001), Medical Devices (ISO 13485), FDA Quality Systems Regulations (QSR), e-record keeping (FDA 21 CFR p11, Annex 11)