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Atlant Systems

PARAFILE

Healthcare & Pharmaceuticals | Clinical Trial Management Software

Product Overview

 PARAFILE

PARAFILE IS AN ELECTRONIC DOCUMENT MANAGEMENT SYSTEM THAT CAN BE TAILORED TO FIT YOUR ENTERPRISE AND EACH DEPARTMENTALLY DIFFERENT EDM REQUIREMENT

paraFile helps users capture, author, edit, distribute, retrieve, and manage electronic documents globally -- documents from any computer source or application.

paraFile truly supports the way people work today. paraFile is "web-enabled" to include internal and external authors, reviewers, and approvers as well as others designated by the enterprise to have access. paraFile is used by many industries to manage critical documents, including pharmaceutical companies who must operate under stringent validation.

Specifications

FEATURES AND BENEFITS

Detailed Audit Trails

Mobile, desktop, and web-based access

Robust security

The Check-in/check-out capability

Version control over content.

Full-Text Search

Collaborative authoring, review, and approval

Mobile Usage of Documents

User-defined content formats

21 CFR Part 11 Compliant

Validated system

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Product Overview

 PARAFILE

PARAFILE IS AN ELECTRONIC DOCUMENT MANAGEMENT SYSTEM THAT CAN BE TAILORED TO FIT YOUR ENTERPRISE AND EACH DEPARTMENTALLY DIFFERENT EDM REQUIREMENT

paraFile helps users capture, author, edit, distribute, retrieve, and manage electronic documents globally -- documents from any computer source or application.

paraFile truly supports the way people work today. paraFile is "web-enabled" to include internal and external authors, reviewers, and approvers as well as others designated by the enterprise to have access. paraFile is used by many industries to manage critical documents, including pharmaceutical companies who must operate under stringent validation.

Specifications

FEATURES AND BENEFITS

Detailed Audit Trails

Mobile, desktop, and web-based access

Robust security

The Check-in/check-out capability

Version control over content.

Full-Text Search

Collaborative authoring, review, and approval

Mobile Usage of Documents

User-defined content formats

21 CFR Part 11 Compliant

Validated system

Add Review

Quality
Facilities
Price
Service
Your Score

Location

Prospect Wiki Ad

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