Alternatives to Ennov Doc

SimplerQMS offers a cloud-based Quality Management Software, specifically designed for the Life Science industry. SimplerQMS helps ensure compliance with various regulatory requirements, including FDA 21 CFR Part 11, EU Annex 11, GxP, cGMP, GAMP 5, GDPR, EU IVDR & EU MDR, ISO 13485:2016, 21 CFR Part 820, and ICH Q10, among others. The system is fully validated according to GAMP5. The system offers a range of Life Science QMS modules such as Document Control, Change Control, Training Management, Supplier Management, Complaints Management, Non-Conformance and Deviation Management, CAPA Management, Audit Management, Technical Documentation Management, Risk Management, Quality KPIs and more. SimplerQMS integrates with Microsoft Office and allows users to work with documents in applications such as Word, PowerPoint, and Excel. Overall, SimplerQMS delivers efficient, paperless workflows that align with the compliance requirements of the Life Science industry.

PDF Extra is an all-in-one suite that enables you to effortlessly read, edit, create, OCR, organize, annotate, fill & sign, convert, and share any PDF. Focused on ease of use, the app has all features you need placed front and center so that you can start using them right away, no manual required. This makes PDF Extra a great choice both for complete beginners and users looking for a powerful and budget-friendly Adobe Acrobat Pro replacement. HERE’S WHAT YOU GET WITH PDF EXTRA: Multiple page view modes and a distraction-free “Read Mode” Advanced editing tools for a Word-like PDF editing experience Two-way conversions: Word, Excel, PowerPoint, or images OCR support: make scanned documents searchable in seconds Markup tools: highlight, comment, strikethrough, stamp, and more Effortless PDF organizer: reorder, compress, split, and combine PDFs Sign & secure: add signatures, fill forms, and protect PDFs with passwords, encryption, and digital certificates Offline mode: work freely on your projects, even when you’re unplugged from the internet

Global OEMs, SaaS and enterprise end-users rely on Adobe PDF Library to automate the creation, editing and management of PDFs. An Adobe partner, our SDK uses the same source code as Acrobat for stability, reliability and quality results. Languages: .NET, .NET Framework, Java and C/C++ Platforms: Windows, Linux & MacOS Package managers: NuGet & Maven Capabilities include but are not limited to: -Annotations -Content creation -Content modification -Color management -Extraction - text, images, forms -Compression/optimize -Conversion - PDF/A, PDF/X, EPS, PostScript, XPS, ZUGFeRD, color -Display, Printing -Extract text, images & other content -Forms - Import, export, flatten static & dynamic XFA forms, AcroForms -Images - extract, import/export, thumbnails, render/rasterize pages, separations -Optimization - size, content, images, etc. -OCR - add text to document, add text to image -PDF to Office Documents (Word, Excel, PPT) -Security - Viewer settings, redactions, password, encrypt/decryption, watermark Pricing options for OEMs, SaaS & end-users are flexible and based on usage. Shorten development times & get to market faster with Adobe PDF Library. Free trial - download today.

SodaPDF is the software solution that will help your business achieve any document goal quickly and easily. You can edit, create, convert and sign PDFs according to your requirements. Use the best PDF editor and converter to modify documents. Our PDF tools are easy to use and can be used to simplify any document workflow. Our Batch tool is the fastest Microsoft Office-to PDF converter on the market. It allows you to create multiple PDFs or convert them all at once. You can also add page numbers, watermarks and Bates numbers to multiple files or folders. Our E-Sign feature allows you to sign, manage and track electronic signatures remotely. OCR Edit saves time and eliminates the need to retype text. It allows you to quickly search, recognize and modify any image or scanned document. Access the entire Soda PDF suite of tools and services from your desktop or any device that has a web browser.

Dot Compliance offers the industry's first ready to use Quality Management Solution powered by the Salesforce.com platform. The Dot Compliance solution includes an extensive set of off-the-shelf ready eQMS and compliance pre-configured processes, enabling customers to deploy quickly and cost effectively. Dot Compliance ready to use solutions include full project validation services and product validation packages. Dot Compliance offers the industry’s most cost-effective quality and compliance management solution available, allowing users to quickly deploy flexible and scalable solutions. Automate core quality processes such as Document Management, Training Management, CAPA, Audits, Customer Complaints, Change Management, Supplier Quality, and more. Our solution is fully configurable and offers seamless integration abilities, with easy adaptation and implementation of customer’s specific requirements.

TLM QMS Software is a powerful and robust quality, risk and material management software (QMS) which is validated and 21 CFR Part 11 compliant. TLM is a cutting-edge, all-in-one quality management system that can be customized to integrate with online CRM software, QuickBooks or ERP databases. Total Lean Management (TLM) QMS Software is specifically intended to be a low cost, highly integrated, flexible and continuously improving landscape to which specialty systems can be added where needed to create the digital business landscape that enables work flows the way your company needs them to work.

Unify quality processes with QT9's all-in-one cloud-based QMS Software Suite. QT9 QMS is a user-friendly quality management software that includes 23+ modules with unlimited scalability. Automate ISO & FDA Compliance with email alerts, To Do lists and FDA 21 CFR Part 11 Compliant Electronic Approvals. QT9 QMS enables Life Sciences, Biotechnology Companies, Medical Device Manufacturers and Pharmaceutical Companies to digitally transform operations. Get real-time status updates and visualize quality metrics up-to-the-minute. QT9 QMS comes with built-in document control, revision-level controls, corrective actions (CAPAs), Nonconforming products and more. Advance product releases with Deviation Management, Engineering Change Orders, FMEA, Inspection Management Modules Included. Go paperless & put time-consuming tasks on autopilot. QT9 QMS comes ready-to-use. Get a free product tour! Start a Free 30-Day Trial. Visit QT9qms.com

Create, review and edit PDF Documents with this full-featured PDF editor available for Windows, Mac, and Linux. PDF Studio is easy to use and a dependable substitute for PDF editors such as Adobe® Acrobat®. It contains all the PDF features and tools needed at a much affordable price, maintaining full compatibility with PDF standards. PDF Studio Standard Features: -Create PDFs -Scan to-PDF -Annotate and markup PDFs -Precision Measuring Instruments -Fill in and Save PDF Forms -Secure Documents -Append/Delete Pages -Create Watermarks, Headers, Footers -Loupe, Pan & Zoom, Rulers, etc... -Document Storage Integrations -DocuSign Integration -Supports PDF 2.0 standards PDF Studio Pro Features: -All features in Standard, Plus... -Interactive Form Designer -OCR (Text Recognition). -Content editing (Text and images) -Redact & Sanitize PDFs -Compare PDFs -Optimize PDFs -Digitally Sign PDFs -Advanced Imposition

Intellect's QMS software has been proven to improve quality operations and reduce overall quality cost by up to 40%. Our apps were designed by certified quality professionals and can be easily customized with our no-code platform or drag-and-drop technology. Remote access for your team, mobile apps, dynamic workflows, analytics, reporting, and remote access are all possible with this modern and simple solution. Apps include Document Control and Employee Training, Audit Management CAPA, Nonconformance, as well as other useful features.

ARMATURE Fabric™, allows you to manage all aspects of your accreditation, certifications, credentialing, audit quality, and compliance activities from one platform. Our software allows you to save time, work more efficiently and securely, and better serve your stakeholders. Whether you manage institutional, programmatic or specialized accreditation programs, certify individuals, products or organizations, conduct audits or assessments, or resolve non-conformances, ARMATURE Fabric can make it simpler and more efficient for both you and your stakeholders. Our cloud-based, secure software allows you to collect data in multiple methods (through online applications and audits, assessments and self-evaluations), manage your accreditation, certification, audit and compliance workflows, capture and manage documents and artifacts and identify and resolve issues; generate reports; and spot trends.

Five of the most important regulatory agencies in the United States use MasterControl Quality Excellence solutions. A leading software-as-a-service (SaaS) provider, MasterControl helps companies get their life-improving products to market sooner. It does this by providing cloud-based solutions that manage an organizations documents, training and exams, corrective/preventive action, validation, and more. MasterControl offers solutions throughout the product's entire lifecycle.

Qualio is a one-stop solution for quality and compliance management. It's ideal for growing companies in healthcare and life sciences. Qualio is reliable, affordable and easy to use. It helps companies build life-saving products faster and achieve 100% ISO, GxP and FDA compliance. Qualio makes it easy for companies to manage document control, training and NCRs, audits as well as suppliers, complaints, and other tasks in one platform.

QEdge QMS is Enterprise Quality Management Software (EQMS). It optimizes quality and ensures regulatory compliance. Enterprise Quality Management Software (EQMS), reduces the risk for quality process failures, lowers overall costs, and makes organizational processes more compliant. QEdge is an EQMS that allows companies to manage their Quality Management System in a disciplinary regulatory environment. It brings together all quality processes, such as Change Control and Deviation, Investigation and Market Complaints. OOS, OOT and Risk Assessment. Document Control activities, Training Records, and Document Control activities. QEdge, an intuitive and configurable software platform, allows for cross-functional communication and collaboration. It can interface with legacy systems and facilitates error-free, cross functional communication.

Ennov Quality Suite. A comprehensive QMS to increase efficiency and ensure compliance. Ennov Quality Suite Ennov Quality Suite combines the power of Ennov Doc and Ennov QMS with Ennov Report and Ennov Training to create an integrated quality management solution that improves operational efficiency and ensures compliance to industry standards like 21 CFR Part 11, GxP, and ISO. Ennov Quality offers a predefined inventory that includes quality documentation, processes, and workflows. These are based on industry standards and best practices. Ennov Quality customers can quickly get their system in production and begin to realize their return on investment. Ennov Quality, as all Ennov solutions, is easy to set up and requires no IT skills. A unified and intuitive content and information management platform that supports and enriches the entire Life Sciences product cycle. Our comprehensive QMS improves operational efficiency

Orcanos is an integrated software solution for ALM (Design Control), and quality management (QMS) that allows you to deliver products on time and within budget. Orcanos is a cloud-based solution that supports Requirements Management and Test Management, Document Control, Risk Management and Quality Management. Orcanos features dashboards and real time alerts to help businesses keep track of their ongoing projects and have real-time visibility on their progress.

ZipQuality, a software-enabled medical device service, helps companies bring new products to the market. Our collaboration platform allows agile teams to make rapid design changes while maintaining regulatory compliance. System (processes and tool) pre-configured; no need to change your quality system. The integrated system is able to handle rapid design iterations in product documentation. Your team will be guided by experienced consultants at every stage. Software tools that are fully featured, scalable, and built on the powerful ENOVIA platform. Our integrated system allows for rapid design changes, while keeping data and documentation in sync. All records are maintained in a audit-ready condition. Product requirements, Hardware requirements, Software requirements. We have a deep understanding of complex, software-intensive devices. ZipQuality is a structured documentation system that supports good systems engineering and efficient risk management. It also provides clear traceability.

Virje complies to 21 CFR Part 11, 21 CFR Section 820, ISO 13485. Are you overwhelmed by the idea of Part 11 software validation Accessible wherever you are, whenever you work. Automated collaboration and automation can help you reduce paper, lower costs, and increase efficiency. This is the ideal solution for small- to medium-sized businesses. This system was designed specifically for quality control of medical devices. The system is flexible enough that it can adapt to your workflows without having to compromise. Modifiable change order approvals can be configured by employee role or by document type. Notifications to the responsible personnel at each stage of the change process. Ability to identify material dispositions for individual documents. Access to historical and released versions of documents is easy. Quick access to document history. Tracking of locations and distribution of hard copies. Notification of periodic document review.

Almond is a cloud-based professional quality management software designed for healthcare companies. The software allows for computerized management of quality processes that are in compliance with regulatory requirements. The system maintains an audit trail of documents, indexes all documents and provides documented evidence for all QMS processes. All information is centralized in a single place. This allows you to manage your suppliers easily. You can give your suppliers permission to conduct training at their premises using your quality system, if it is required by your system. Receive automatic emails before the expiration of supplier certification. You can be informed at any time about the status of your project using an electronic control dashboard. You can create as many logbooks you need without any budget or storage restrictions. Automatic conversion from ineffective to effective after training completion.

Pharmaceutical and Biotech companies face challenges in meeting control documentation requirements in their day-to-day operations. Document management and control are essential components of any quality and compliance solution. Global Regulatory agencies expect all regulated companies to follow industry best practices during the manufacturing process. Phama Soft Sol created Document Management System software to help manage and distribute SOP's, STP's, and other regulated documents. Document management software systems can not only lower compliance costs but also improve product quality and process efficiency. Document Management System (softDMS) allows you to quickly retrieve the information you need, at the exact time you need it. This reduces the risk of miscommunications and errors which in turn minimizes risks, manhours, and other documentation errors.

Organizations need to standardize their business processes and automate them in order to bring new products to market quickly and comply with global regulations. QUMAS EQMS (formerly ProcessCompliance), a cloud-based solution that provides integrated regulatory, quality and compliance management capabilities within a validated QMS environment, is QUMAS EQMS. QUMAS's data-centric approach lets you manage quality content easily and access and re-use all data. This gives you a comprehensive view into Quality. Interactive quality dashboards from QUMAS provide QMS overviews across all business areas and quality initiatives. Export, email, and scheduling are all possible for reports. QUMAS allows QMS departments the ability to securely, efficiently, and compliantly exchange information in the cloud.

Vault QualityDocs provides automated workflows and audit trails that provide detailed audit trails. This reduces compliance risk and improves quality. It speeds up review and approval and facilitates the sharing SOPs and other GxP documents between employees and partners. Effective SOP management is made easier by automated workflows and visibility to the content status and processes. This reduces compliance risk. An intuitive, user-friendly interface is key to adoption and efficiency. Audit trails with detailed audit trails, content organization, powerful search, and robust search allow for better inspections and audits. You can securely access and use any web browser. If enabled, you can also print, distribute, track, and track the control of PDF copies. Pre-defined metadata and document taxonomy allow for operational harmonization. Organizations can quickly adopt best practices by using pre-defined pick lists for quality, manufacturing and validation documents.

Quality Link 7 is a combination of people and technology. It builds on our proven platform to help organizations automate processes, save time, and comply with regulatory requirements. Quality Link's document management system improves efficiency and eliminates the need for manual paperwork. This module will store and manage every document you create. This module allows you to print "uncontrolled" copies and perform other document-related tasks. You'll see a reduction in clerical tasks for quality staff by up to 90% with the improved organization. Our software converts existing documents from your previous management system and requires no learning curve. You won't have to lose your favorite applications as they can be easily integrated. Quality Link makes manual document maintenance obsolete and eliminates the need for constant monitoring.

We offer solutions to companies that have a high standard of quality. Our software solutions are characterized by a modern UX and useful functionality. They also feature high modularity and consistent compliance. Integrated solutions to manage quality and ensure quality. Focused on digitizing controlled documents and QA process. Solutions designed specifically to meet the requirements of the financial sector for written rules of procedure and management of policies. Cloud-based, prevalidated solution for automating your validation processes as well as digitally controlling and managing validation documents. Early setup of a digital quality management system with a solution that is tailored for startups and young businesses. Based on DHC VISION. It is ready to use, with immediate compliance. No license fees. Together, we digitize the quality management and quality control processes and ensure regulatory compliance.

Greenlight Guru is the only product development and quality management platform designed specifically for medical device companies. The Medical Device Success Platform helps companies get safer products to market faster, simplifies FDA and ISO regulatory compliance, and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits, document control, training, design control, and more. Device makers across the globe are replacing their outdated paper-based and general-purpose legacy quality systems with Greenlight Guru to push beyond baseline compliance and achieve True Quality.

A well-implemented Quality Management System (QMS) is essential for biotech firms to achieve regulatory compliance. It will also help them maintain product quality and safety. It will also help them manage risks effectively. It will drive operational efficiency. InstantGMP QMS was designed by quality and regulatory professionals for biotech companies. It is simple, affordable, and complete. It can be used by small-to mid-sized manufacturers in many different industries. This quality management software features guided workflows to reinforce adherence with government standards during the entire production process. It also has a variety of innovative features and specialized module. Maintain and improve the safety and quality of biotech products. Frameworks are provided for identifying, assessing and mitigating risk throughout the product's lifecycle to reduce the likelihood of quality incidents or product recalls.

The AssurX platform is a powerful software platform for enterprise quality management (EQMS) and regulatory compliance to reliably communicate and coordinate information, documentation, and activities. AssurX allows regulated businesses to quickly identify and control quality issues and risk exposure to avoid quality or noncompliance problems while improving workflow. AssurX QMS software is uniquely configurable to fit any established or dynamic business requirements. The system creates an electronic workflow of tasks, alerts, escalations, and approvals that can be automated to the desired level, mapping precisely to real-world operations. No other system is easier to deploy, configure, and modify. AssurX solutions integrate seamlessly to create a connected quality system. Solutions include audit management, corrective actions, training management, compliant management, document management, change control, risk management, EHS incident management, and more.

Founded in 1989, InfinityQS is the leading provider of Statistical Process Control (SPC) software and services to manufacturers worldwide. ProFicient on Demand automates data collection and analysis during the manufacturing process so you can make real-time process improvement decisions—and prevent defects before they occur. Developed by industrial statisticians using proven methodologies for quality analysis and control, InfinityQS solutions save leading manufacturers millions of dollars each year.

Clinevo OneQMS, a cloud-based system for quality management, allows organizations to manage compliance and quality processes digitally. Clinevo OneQMS provides an interactive platform for managing all quality and compliance processes within an organization. OneQMS allows organizations to manage documents and training, changes, CAPAs, and audits all in one place. It can be accessed using IE, Chrome and Firefox browsers. Dashboards and reports that are powerful and actionable for real-time monitoring of compliance and quality. Clinevo can be taught to business, quality, IT, and other teams within a few short hours. Clinevo OneQMS is compliant with all current and new regulations. It comes with a built-in training management system that allows the organization to manage its training processes efficiently. It is the best QMS and comes with transparent, optimized pricing.

Your static PDF content can be brought to life. Responsive digital publication. The web PDF viewer and digital publishing software. Your brochure, magazine, or catalog can be converted into a responsive online publication. Convert PDF documents to interactive online viewing. This web-based PDF viewer is designed for magazines, catalogs, and other high-quality print documents. It allows you to publish your publications online and preserves the original layout. This viewer can be embedded to provide seamless viewing for your visitors while they flip through your publication. To achieve maximum readability, speed, and text sharpness, convert your PDF catalogs into HTML5. This viewer optimizes your PDF files for online use and minimizes the loading time. The viewer offers both flipbook and slide viewing options.

Haihaisoft Reader is a PDF document reader and printer that is free. It has a fast launch speed and rich feature set. It can also be used to read PDF documents protected by DRM-X. It is now available on Windows, Mac, Android, iPhone/iPad, and Android. Adobe Acrobat allows you to open and print all Adobe PDF documents. Haihaisoft Reader's download size is just 3 MB, which is less than Adobe Reader. We understand privacy and security are important to you. Haihaisoft PDF Reader respects users' privacy and security. It will never connect to the Internet without their permission. Haihaisoft PDF Reader does not connect to the Internet in background to protect your privacy. Just check the version and then update the software by clicking the help menu. DRM-X platform makes it easy for everyone to set different rights permissions and securely share documents.

This PDF utility is the most reliable and allows you to edit PDFs quickly. Be it your office documents, educational documents,receipts,bills,certificates,ID cards, you can edit them all. This PDF utility is lightweight and completely free. It can also work offline. The app now includes a PDF Reader that allows you to view edited files. The PDF Editor is easy to use and includes the following features: Modify and create PDFs; Open and view PDFs using the free PDF viewer. You can adjust the content of your document to make it easier to read. Combine PDF or images (JPG/PNG/BMP/TIFF), into one PDF. The PDF Merge feature allows you to merge PDFs from your local storage. It can also merge documents on the cloud. Split PDF into smaller PDFs to reduce its size. PDF Split allows you to extract PDF pages by specifying a range.

Free PDF Printer allows you to print to PDF documents from any Microsoft Windows application. Supports Citrix Metaframe and Microsoft Terminal Server environments. PDF Studio is a fully-functional viewer, merge, splitter, and splitter for PDF files. It allows you to view, search, print, merge, split, and reorder PDF documents. You can install a virtual printer to create a Microsoft Word document, instead of a piece paper. You can print directly from Windows to a.doc document and then edit the content. This program can convert existing PDF documents into Microsoft Word format. The program can convert your PDF documents to Microsoft Word format so that you can open and modify the resulting documents in Word. Your database can be brought online in seconds. Live reports and searches can be created without programming. Supports Sage, Dynamics and Access, MSSQL MySQL, Access, MSSQL, Access, and other ODBC-compliant databases.

Professional tool to create, convert, edit, and annotate PDF files. GoodReader®, a file viewer, has many powerful features. Most of these features address PDF and TXT viewing. GoodReader®, a powerful PDF editor app for iPad, iPhone, and iPod touch is available. Its iPad version was the #1 non-Apple iPad app in 2010, and we have been constantly improving it to make it the best mobile productivity tool available. We have many more features to come! GoodReader for iPad/iPhone allows you to read almost anything anywhere, including books, movies and maps. Once you use it, you'll be hooked. If you work with documents, you'll soon wonder how you ever managed without GoodReader. GoodReader can automatically synchronize individual files and entire folders to remote versions hosted on an online server. GoodReader supports email server access and email attachment downloads.

OnePDF is an online tool that allows you to view and convert PDF documents quickly and easily. OnePDF's Excel-toPDF converting tool is one of its most impressive features. It allows you to quickly convert Excel files into high-quality PDFs. OnePDF's Excel to PDF converting tool makes it easy to convert Excel files without the need for additional software or complicated installations. Simply upload your Excel file to OnePDF and the tool will convert it into a PDF document in a matter of seconds. The converted PDF file can be downloaded and used however you wish.

ACE Essentials is the pre-validated Electronic Quality Management System Software (EQMS) designed for highly regulated industries. ACE Essentials includes 10 workflows, as well as all the required Standard Operating Procedures (SOPs) and Policies. This ensures that your quality management system is fully compliant from the start. ACE Essentials features include a complete audit trail that tracks every action within the system. This allows you to understand the risks associated assets. Features of ACE Essentials Pre-Configured Workflows Pre-Configured Event Management (Due dates, Scheduling, Reminders) - Pre-Configured Permission Based Security - Pre-Configured Full Documentation - 50+ documents - Multiple Site Capability - No Charge Upgrades for the Product's Life Pre-Configured Tasks Liste - No Validation Period Pre-Configured In System Notifications Pre-Configured Email Notifications

UniPoint's Quality Management Software can be used on-premise to manage quality. Quality Management Software is easy to integrate with other ERP systems. Quality Management Software can be used by manufacturers of any product, in any manufacturing mode. With Quality Management Software, users can manage processes such as document control, equipment management, non-conformances, corrective/prevantative actions, and more.

Document control made easy. You can create, review/approve and revise documents, as well as retire them. All transactions are recorded using e-signatures, timestamps, and stored in the Audit Trail. Audits from start-to-finish The SOLABS QM10 Audit APP allows you to track and document all aspects of your audits, from planning and preparation to closing. The SOLABS QM Essentials package offers advanced reporting capabilities and intuitive reporting. Trending and tracking are critical components of any quality management system. The dashboards and reports are easy-to-use, customizable, and can be shared in the most popular formats such as Excel, PowerPoint and PDF. You can share the reports and dashboards with anyone in your organization. In a matter of seconds, you can create, schedule, monitor, and assign training. Online assessments can be used to validate the learnings of your team. You can manage all aspects of training with the SOLABS QM Training section.

ZenQMS improves the quality compliance profiles life sciences companies through a cloud-based platform. It is purpose-built to facilitate document collaboration, control, training, issues management, audits, and change management. ZenQMS is a team of technology and quality leaders who share the common goal of making quality management a business imperative.

Ideagen Quality Management, a modular SaaS application, is designed with quality managers in mind. More than 6,000 customers trust Ideagen Quality Management to digitalize and comply with industry standards. Ideagen Quality Management integrates seamlessly with your existing processes, and is the backbone of your business. Our system's workflow automation and comprehensive documentation management empowers your team by identifying and resolving any issues before they occur. Our powerful digital quality management software will help you to improve your organization's performance, and give you a competitive advantage. Our software helps you gain full visibility of your organization, identify risks and take action, and maximize opportunities. Secure world-class processes and smart data-driven decisions that will satisfy your customers, regulators, and grow your business.

QualityKick provides a QMS solution for the biological sciences. It is divided into different modules, each of which solves a particular part of the quality-management processes: document control and control of training, change control and control of events, CAPA and risk assessment, as well as audits and qualification of suppliers and equipment. It is a web application that can be accessed anywhere and on any mobile device. It works on all devices: computer, tablet, and smartphone. A guided tour is automatically loaded when new users sign in. You can edit documents in MS Word, and then send them to a configurable review process. You can configure different types of events, such as deviations or nonconformities. CAPA plans can be defined, actions recorded, and their effectiveness verified. Solutions for quality management within the pharmaceutical, biotechnology and medicine sectors.

SoftExpert EQM (enterprise quality management software) is the most comprehensive. It assists companies in achieving and maintaining ISO 9001 certification by automating highly interactive quality processes that are tailored to their specific products, operations, and business practices. As a modular and scalable solution platform, SoftExpert Quality Management Software seamlessly integrates all key quality initiatives, including process mapping, documented information (SOP - standard operating procedures, work instructions and records), non-conformance reports (NCR/NCMR), corrective/preventive actions (CAPA), quality indicators (KPIs). The solution can also manage supplier relations, customer complaints and quality audits, as well as competence and training, quality controls, quality inspection, and statistical process control, increasing QMS flexibility and robustness.

Your team should keep your device history file (DHF), while it is being created. MatrixALM can help you verify the content and assist you in creating documents for certification. Work instructions and processes should be simple, efficient, and easy-to-use. Not SOPs written by someone else. MatrixQMS can help you create a quality management system that works for and against you. Risk management must be integrated into the design process as well as the quality system. Not in Excel files on some servers. The traceability matrix includes the risks associated with our applications. Not when you think your device is ready for release, but while you plan and document your validation and verification activities. MatrixALM provides the complete traceability matrix, from the requirements to the completed tests.

Revolutionize your Life Sciences processes. You can dramatically improve the quality, control, and efficiency of your products and processes. Our fully compliant platform is pre-validated according GAMP5. This ensures inspection readiness at all time. You have complete control over all documents and processes. You can also customize workflows and automate when possible. You can enjoy uninterrupted workflows and full traceability with seamlessly connected and integrated modules. Our dedicated team is available to answer any questions you may have. Only the best Scilife experience is possible! Our Scilife platform automates, automates and organizes all processes in your industry space, no matter if you're in Medical Devices or Pharma & Biotech or ATMP. Click below to see which Scilife modules are available for your industry's unique lifecycle stages.

LabWay LIMS allows you to focus on what you do best, and manage your lab. Integrated digital solutions to organize and manage laboratory information. LabWay LIMS is a LIMS and QMS solution that allows for the computation of all laboratory areas. Its main goal is to promote productivity and process quality improvements. LabWay is a highly-competitive LIMS and QMS for different areas of activities. Proactive communication system, control of records for pending activities and process. Quick and easy-to-use integrated document management that provides verification and evaluation of purchases and orders. Management of internal and outside audits to ensure continuous improvement. Team management that is both efficient and fast. We align management strategy with quality. Management of immediate action and effective resource management. Improved service quality and speed in sending results.

RQM+, a global service provider for medical technology, is focused on accelerating market success and compliance. We deliver specialized solutions to medical technology companies and accelerate the journey along the entire product lifecycle, from concept through commercialization and post-market. Our portfolio of services allows us to deliver end-to-end products and solutions throughout the entire medical device lifecycle. RQM+ quality assurance engineers review materials lists, establish suppliers, and support design change processes. RQM+’s design quality engineers support any packaging, sterility or biocompatibility testing that may be required. RQM+ regulatory affairs consultants offer guidance and assistance with submissions to FDA, notified authorities, or other government agencies. Our extensive experience with the most recent reimbursement requirements and value based compensation models is what we use.

You can now focus on delivering safer and more effective products faster by eliminating repetitive, manual tasks. SmartSolve Postmarket Suveillance by IQVIA is a SaaS solution for postmarket surveillance. It provides best practices for centrally managing all postmarket surveillance activities. Fusion is a SmartSolve/RIM Smart user event. It provides in-depth education on timely and relevant quality topics and regulatory topics, as well as practical insights and tools that can be used within any Life Sciences organization. Fusion began as a live SmartSolve user event. It has expanded over the years to include both virtual and live events for SmartSolve and RIM Smart users. IQVIA SmartSolve™, Regulatory Connector, simplifies, automates, and integrates your compliance response times. Connected Intelligence, our innovative, interconnected approach to operational efficiency, is what we call Connected Intelligence.

A digital quality ecosystem that delivers proactive quality. TrackWise Digital, a cloud-based, industry-leading quality management system, has integrated modules that support quality, compliance, and more efficient and effective decision-making. Users can use quality data to improve their culture of quality and increase company performance through advanced analytics and reporting across all quality processes. TrackWise Digital's Quality Process Accelerators, (QPAs), are based on Sparta’s 25+ years of expertise. They provide quick value and streamline digital quality. TrackWise Digital's QMS is the first to use AI to enhance quality-related decision-making capabilities. This allows for a shift in quality from reactive to proactive.

Advantum's flexibility and security make it the perfect solution to your information management needs. You can choose from pre-packaged solutions or individual components. Or, let us design something that is unique to your needs. We will provide cost efficiency, reliability, and custom configurations. It is easy to work anywhere you like today. Advantum can be used on any device, including your smartphone or tablet. Advantum's flexibility allows you to tackle the challenges of today while still being prepared for future technical and organizational changes. Advantum is flexible, as is its licensing model. Flexible licensing is used and we focus on concurrent users. Advantum is a cost-effective option for you by sharing licenses. Our customers appreciate our support the most.

Your customers and shareholders will be delighted by your profitable products Buyers have changed. Supply chains are in chaos. The definition of a product is being redefined. However, product development technologies have not kept pace. We need a new approach. One that is focused on patient and customer outcomes. This helps product companies make the right decisions. This engages markets with engaging products and experiences. This is called product value management (PVM). Collaboration with all stakeholders, including suppliers and customers, is essential to develop and launch innovative products. Design for product quality and manage part quality. Take action to resolve quality issues. To engage customers with enhanced omnichannel product experiences, leverage a trusted source of product information.

EzyPro Adaptive Management system QHSE (QHSE) enables you to seamlessly integrate compliance, performance and continuous improvement. EzyPro QHSE is a one-stop solution for compliance, maintenance and operational control. You can increase efficiency, share information, collaborate, and increase productivity. Flexible subscriptions are possible with its modular approach. EzyPro Healthcare – Hospital Quality Management System with integrated action tracking, dashboards and dashboards to meet requirements such as NABH or JCI. As a central hub for continuous improvement across the Healthcare unit, it was designed. Remote consultancy service is available for implementation support. QHSE Management System bundled comprehensive maintenance management solution. Increase equipment lifespan, increase time efficiency, and equipment uptime. This will result in lower costs and higher profits. You can easily manage work orders for repairs or maintenance, as well as transfer of assets, using a QR code assisted asset retrieval.