Best Document Management Software - Page 61

Pype

Reduce project risk and strengthen client relationships by automating processes that are critical for owner satisfaction and contract compliance.

Pyraman - Document Management System

Pyraman is a cloud-based eQMS platform that helps manufacturing, automobile, aerospace, food, pharma, and IT businesses manage documents, records, audits, non-conformances, complaints, and training; all in one place to simplify ISO/IATF/AS9100 compliance.

QBD.Net

qdoc

QM

QM is an integrated, scalable enterprise quality management software (EQMS) that helps Life Sciences companies improve their operational efficiency and maintain compliance with GxPs by automating quality operations with respect to FDA 21 CFR Part 11 and Annex 11.

QT9 QMS

QT9™ QMS is your all-in-one quality management software. Centralize more quality data metrics than any other platform standard. Easy-to-use & ready-to-go. Fully-validated. Start a trial. All-In-One QMS QT9 provides an integrated solution with 25+ quality modules that include Document Management, Maintenance, Product, Customer, Supplier, Employee Training, ISO, FDA and regulatory compliance automation. Be more efficient with electronic signature approvals, dashboards, automated reminders, multi-site ready, approval management, web portals, user to-do lists and more. Simplify Compliance Make audits easy with one central place to see real-time data for FDA 21 CFR Part 11, FDA 21 CFR Part 210/211, FDA 21 CFR Part 820, ISO 9001, ISO 13485, ISO 14001, ISO 17025, AS9100, HACCP and SQF. Ideal for Life Sciences, Biotechnology, Medical Device Manufacturers, Pharmaceutical Companies, Laboratories, Aerospace and Defense Companies and Foods. Easy-To-Use QT9 QMS is easy to setup and use. See a demo and get started with a free trial today. We offer lots of resources including: QT9 Help, Training Academy, Support Requests, Training Webinars, Content Customization, Free Maintenance, Unlimited Training and Unlimited Support. For more information, visit QT9software.com.

Average Rating: 4.8/5.0

Total Reviews: 129

Qualiex

Qualiex is a comprehensive Quality Management System (QMS) designed to centralize critical processes within a single platform, connecting planning, execution, and continuous improvement to deliver full control, ensured compliance, and measurable results. Built for organizations that need to scale operations with security and traceability, the platform eliminates information silos, automates workflows, and provides real-time data to support safer, more strategic decision-making. More than 100,000 quality professionals rely on the platform to streamline processes, strengthen governance, and improve operational efficiency. Unlike fragmented tools, Qualiex delivers a fully integrated quality management experience, enabling organizations to connect analyses, action plans, risks, and strategic initiatives within a centralized environment. Core Capabilities - Intelligent document control with complete traceability - Risk management supported by structured methodologies - Action plans aligned with business strategy - Predictive dashboards with automated insights - Supplier management with continuous evaluation - Incident management and root cause analysis - Workflow automation to eliminate manual tasks - Performance indicators that drive continuous improvement Result: less rework, greater operational visibility, and a data-driven quality culture. Qualiex follows internationally recognized standards and operates on a highly secure cloud infrastructure with encryption, automated backups, and high availability — ensuring business continuity and data protection for regulated environments. When to choose Qualiex? ✔ replace spreadsheets and manual controls ✔ ensure regulatory compliance ✔ increase operational efficiency ✔ strengthen governance and risk management ✔ turn nonconformities into continuous improvement opportunities Manage all your tasks (yes, all of them) right in the palm of your hand in App! So if you have a task in any module of our suite (Minutes and Decisions, Audits, Suppliers, Plans, Incidents, or Risks), you will be able to interact with it, whether by changing its status or even reporting progress and cost.

Qualio

Qualio is a quality management and compliance platform built exclusively for life sciences companies. It helps medical device, pharmaceutical, biotech, and digital health organizations accelerate regulatory approvals, stay audit-ready, and scale compliance operations without adding headcount. Our platform manages the full range of quality processes, including document control, training, CAPA, change control, supplier management, risk management, and design controls, all in one validated system, supporting FDA 21 CFR Part 11, ISO 13485, EU MDR, MDSAP, GxP, ICH Q10, and other life sciences requirements. Move faster without compliance as the bottleneck. Qualio connects regulatory affairs, quality, and R&D in one platform, with deep integrations into Jira, Azure DevOps, GitHub, Salesforce, and other tools teams already use, removing the handoffs and manual documentation that typically slow product development down. Get to market faster. Automated gap analysis and multi-framework compliance mapping cut audit preparation time by 80%. Reusing evidence across FDA, ISO, and EU submissions has helped customers shrink market entry timelines from 9 months to 3-4 months, while cross-mapped documentation accelerates 510(k) submissions, CE marking, and international expansion. Scale without growing your compliance overhead. Customers report a 99% reduction in quality administrative time and have eliminated $150K-$300K in annual consulting costs by replacing manual processes, driving 5X ROI within 2 months. See risk before it becomes a finding. End-to-end traceability connects requirements, risk assessments, CAPAs, and product changes, with risk-based alerting that flags gaps before they turn into FDA 483 observations, warning letters, or audit findings. Customers have passed ISO 13485 certifications and sponsor audits with zero major nonconformances using this always-on monitoring. Qualio serves life sciences companies from pre-market startups to established enterprises, with the SOC 2, HIPAA, and pharmacovigilance capabilities growth-stage companies need, deploying faster than legacy eQMS vendors while maintaining the validation rigor required for FDA inspections and notified body audits.

Average Rating: 4.4/5.0

Total Reviews: 776

Quark Docurated

Quark Docurated is a centralized, AI-driven sales enablement platform for sales, marketing and knowledge teams to securely find and share content, manage assets and track all engagement and performance with next generation content intelligence.

Average Rating: 4.5/5.0

Total Reviews: 4

QuicklyDoc

Quince Solutions

Quince Solutions offers a range of Software Solutions that enable your organization to manage and leverage your information effectively. Quince Solutions is an expert in designing and implementing Enterprise Content Management, Business Process Management, and Case Management solutions built on industry leading platforms.

R2 Docuo

Cloud-based document management and workflow platform. R2 Docuo helps organizations manage contracts, invoices, quotes, and business processes through ready-to-use apps or fully customized solutions. Store, organize, and share documents with advanced metadata, version control, templates, and powerful search capabilities. Automate approvals, reviews, and other recurring workflows while connecting information across departments. For organizations with more complex requirements, R2 Docuo provides configurable modules, API access, and industry-specific business solutions built on the same platform. AI-powered document processing helps classify, extract, and retrieve information faster.

Average Rating: 4.5/5.0

Total Reviews: 99

Rabaed

Rabaed is construction document management and approvals software built in Saudi Arabia for the three parties of a construction project: the owner, the consultant and the contractor. It replaces the paper cycle of printed, signed, stamped and hand-delivered forms with one documented, time-stamped project record that all three parties share. Rabaed is organised in four modules on a single record. Official correspondence: every letter between the parties carries an automatic reference number, with the dates of sending, receipt and reply recorded. Approvals and requests: material submittals, work inspection requests (WIR), material inspection requests (MIR) and non-conformance reports (NCR) move through four recorded steps: sent, received, reviewed, and approved or rejected with comments. Receipt is acknowledged automatically with the name and time of the receiver. Consultants can inspect on site from a mobile phone and attach photos to the request, and the decision is issued as a stamped PDF. Daily site reports: weather, workforce, equipment and the day's activities, with photos, kept in the same project record. Documents and revisions: a controlled register where the latest approved revision is the one the site sees, while earlier revisions remain in the record. Each party keeps a private internal review cycle. Drafts, internal comments and the number of review rounds never cross to the other parties; only the official transaction does. Permissions are defined per organisation. Forms follow the templates used in Saudi construction projects and are customised for each project. The interface is Arabic-first, with English available for non-Arabic-speaking engineers on the same project. Compared with the paper cycle on the same project, Rabaed's measured results are: approvals and inspections 3.6 times faster, document retrieval 7 times faster, 31% less time on administrative tasks, and a 22% improvement in document governance. Activation takes days, on site, without stopping work: the project starts from where it stands today, and each team gets one 15-minute introduction session. A single project subscription covers all parties and users. The record belongs to the project owner and remains available after the project ends. Rabaed comes with a 60-day full money-back guarantee.

RadaeePDF

Use RadaeePDF SDK in the applications you develop for your customers and in your software products to deliver rich, complete PDF file management capabilities. Your applications will display, edit, annotate, sign, and manipulate any PDF file. Your microservices will generate PDF/A files, convert DOCX documents, and optimize files and reports for archiving and web delivery. Trusted by organizations such as IEEE, Namirial, Bank of Scotland, Apparound, IBM, and Deutsche Bahn, as well as small and medium businesses and startups worldwide. Available on Android, Windows UWP, iOS, and Linux through native languages and cross-platform frameworks.

Average Rating: 4.3/5.0

Total Reviews: 2

RamBase