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softDMS

by Pharma Soft Sol · Since 2012
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ActiveAvailable globallyCloud
Quick facts
VendorPharma Soft Sol
Year launched2012
StatusActive
LocationD.No.1-121/63 3rd Floor, Main Road, Behind Hotel Sitara Grand, Miyapur, Hyderabad, Telangana - 500049
Countries servedGlobal
Languages9
Integrations
Free tier
Free trial
Contact salesYES

About softDMS

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softDMS is a specialized Document Management System (DMS) crafted for the highly regulated pharmaceutical and biotech industries. Its core purpose is to help companies meet stringent documentation requirements for materials like Standard Operating Procedures (SOPs) and Standard Testing Procedures (STPs), which are critical for quality and compliance. The software's design prioritizes a user-friendly and intuitive experience, aiming to simplify complex documentation workflows. It is presented as an "easy tool" that automates key processes, such as document initiation and approval, with a clear emphasis on creating a "paperless solution." The system's functionality is robust, including features like email alerts and notifications to keep users informed, a master list view and search for authorized users, and a secure revision control system. These features are designed to minimize miscommunication and errors, ensuring the right documents are available at the right time. The performance and reliability of softDMS are central to its value proposition. The software is built to efficiently retrieve information precisely when needed, thereby minimizing risks and reducing man-hours.

Pros & Cons

What users like
  • +Specifically built for pharmaceutical and biotech regulatory needs
  • +Strong document version control and audit trails
  • +Automated alerts minimize missed deadlines
  • +Secure, role-based document access
  • +Supports online and department-level document sharing
What users flag
  • No clear public pricing
  • No confirmation of cloud availability — might be on-premise only
  • Limited info on integrations
  • No in-app marketplace or extensibility options
  • The software is highly specialized for the pharma and biotech industries, which may limit its use for other types of organizations.

Features

Key features

Document Initiation and Approval – Streamlined process for creating and approving documents.
E-Mail Alerts and Notifications – Automated alerts for document status changes and due revisions.
Document Master List & Search – Easy access and retrieval of approved documents.
Revision Control – Ensures only current versions are in use.
Audit Trails – Complete tracking of document history for compliance.
Controlled Document Access – Role-based permissions for secure document handling.
Integration with Other Applications – Can work alongside other enterprise systems.

Additional features

Document initiation, review, and approval workflow
E-mail alerts for activities, revisions, and overdue tasks
Training linkage for document approvals
Master document list and search function
Department-level document distribution and printing
Version control for up-to-date availability
Tracking and reminders for document revisions
Approved document search and retrieval
Audit trail for compliance audits
Controlled and secure access for authorized users
Multi-document handling and status view for controllers
Paperless review and approval process
Automatic master list updates
Online sharing and viewing of documents
Access to documents anytime, anywhere
Data possession assurance for users
Integration with other applications

Pricing

Free trial
Free version
Request a quote
Promo Offer

Countries & Languages

Global
Countries served
9
Interface languages
15
Billing currencies

Interface languages

EnglishSpanishPortugueseGermanFrenchItalianDutchRussianChinese

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇨🇦CAD🇦🇺AUD🇯🇵JPY🇨🇳CNY🇨🇭CHF🇮🇳INR🇲🇽MXN🇧🇷BRL🇷🇺RUB🇰🇷KRW🇹🇷TRY🇿🇦ZAR

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