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What is SOFTDMS?

Pharmaceutical and biotechnology companies encounter numerous obstacles when it comes to maintaining control documentation standards in their everyday functions. The effective management and regulation of documents play a crucial role in establishing a robust quality assurance and compliance framework. Regulatory authorities worldwide require businesses operating in regulated sectors to comply with the most recent best practices in their manufacturing operations. To tackle these issues, Pharma Soft Sol has developed a Document Management System (DMS) tailored to enhance the control and distribution of Standard Operating Procedures (SOPs), Standard Testing Procedures (STPs), and other critical documents. Such document management solutions not only reduce compliance expenses but also improve process efficiency and product quality significantly. The softDMS is crafted to ensure timely access to vital information, which minimizes the chances of errors and miscommunication, thereby lowering risks, labor costs, and document inaccuracies. Organizations that adopt this system can expect to experience a more streamlined operation that is in line with regulatory requirements, while also promoting ongoing improvements in their workflows. Ultimately, the implementation of such technological advancements sets the stage for long-term success and adaptability in a fast-evolving industry.

What is Orcanos ALM and QMS?

Orcanos provides a robust software solution designed for Application Lifecycle Management (ALM) and Quality Management Systems (QMS), ensuring that products are delivered on time and within budget. This efficient cloud-based platform integrates functionalities such as Requirements Management, Test Management, Document Control, Risk Management, and Quality Management into a single repository. Users benefit from intuitive dashboards and real-time alerts that enhance project monitoring and visibility throughout the development process. The Orcanos e-DMS serves as a comprehensive document management system, enabling users to create, track, search, archive, and approve documentation critical to each stage of medical device launch. By streamlining access to essential documents related to planning, design, development, manufacturing, and servicing, the e-DMS improves the efficiency of quality processes and significantly reduces time to market. Furthermore, this optimized workflow empowers organizations to prioritize innovation and adhere to regulatory standards while maintaining high levels of productivity, ultimately fostering a culture of continuous improvement.

Media

Media

Integrations Supported

Jira
Microsoft 365
Salesforce

Integrations Supported

Jira
Microsoft 365
Salesforce

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

$69.00/month/user
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

Pharma Soft Sol

Company Location

India

Company Website

softdms.com

Company Facts

Organization Name

Orcanos

Date Founded

2004

Company Location

Israel

Company Website

www.orcanos.com/compliance/qpack-medical-compliance/

Categories and Features

Pharmacy

Automatic Refills
Barcode Generation
Claims Management
Compounding
E-Prescribing
Electronic Signature
Forms Management
Insurance Processing
Inventory Management
Multi-Store Management
Online Refills
Pill Database
Pill Imaging
Point of Sale (POS)
Prescription Processing
Rx Image Scanning
Signature Capture

Categories and Features

Application Lifecycle Management

Administrator Level Control
Defect Tracking
Iteration Planning
Project Management
Release Management
Requirements Review
Task Management
Test Case Tracking
User Level Management
Version Control

Requirements Management

Automated Functional Sizing
Automated Requirements QA
Automated Test Generation
Automated Use Case Modeling
Change Management
Collaboration
History Tracking
Prioritization
Reporting
Status Reporting
Status Tracking
Summary Reports
Task Management
To-Do List
Traceability
User Defined Attributes

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