Alternatives to MediaLab Document Control

Intelex delivers a unified software system for overseeing Environmental, Health, Safety, and Quality (EHSQ) initiatives. Its expandable platform is crafted to consolidate, oversee, and scrutinize EHS and Quality data comprehensively. The solution works on any device to meet the realities of your workplace. With Intelex, your organization can: Elevate your EHSQ program outcomes by supervising workflows for superior performance and command. Discern patterns and propensities through goal-setting to deepen understanding and improve decision-making in your EHSQ program. Diminish occurrences and cut down on administrative tasks by efficiently supervising, managing, refining, and extracting insights from your safety data via our intuitive safety software. Simplify the management and reporting of air, water, and waste emissions, and oversee environmental outputs to fulfill sustainability objectives. Foster ongoing improvements in quality by seamlessly logging and monitoring all instances of nonconformity within a unified, web-based system. Investigate trends across various departments, sites, or locations. Intelex can help you manage compliance with international standards and regulations such as: OSHA, WCB, ISO 45001, EPA, ISO

Adaptive Compliance Engine® (ACE®) is a highly configurable, workflow based eQMS/eDMS and more that can adapt to any business process, allowing for real-time tracking, management, and reporting of all compliance, quality, and operational activities. With ACE®, you will minimize the administrative hassles and maximize ROI with productivity gains from day one – all while 21 CFR Part 11 compliant. Our one-stop software includes: -Office 365 Integration -Inspection Management -Document Management -Risk Management -Product Lifecycle Management -Learning Management -Audit Management -Quality Events -Paperless Validation -Electronic Signatures (21 CFR Part 11 Compliant) -Endless Workflow Configurations -And so much more! Empower all levels of your organization with intuitive user interfaces, easily search for all your documents and records, and transform your data into actionable intelligence with advanced analytics all on a single platform. ACE comes with everything you need, all included at one price. Every application is included, no more a la carte pricing. No more nickel and diming. One software, endless solutions.

Artintech ERP is a comprehensive enterprise resource planning solution designed to optimize and streamline your business operations across various departments. Tailored for small to medium-sized enterprises (SMEs), Artintech ERP offers robust functionality with a user-friendly interface, allowing businesses to seamlessly manage their resources, inventory, human capital, finances, and customer relations all in one integrated platform. Why Choose Artintech ERP? * User-Friendly Interface: Designed for ease of use, Artintech ERP minimizes the learning curve, ensuring a smooth transition and quick adoption across your organization. * Cloud-Based Flexibility: Access your ERP system anytime, anywhere, with our secure cloud-based solution, which provides the flexibility to manage your business on the go. * Comprehensive Support: Our dedicated support team is available to assist you every step of the way, from initial implementation to ongoing maintenance and updates.

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 25+ 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 Trial. Visit QT9qms.com

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.

Qualtrax is a quality and compliance software program that can manage and control documentation, automate key business processes, streamline training management, manage external and internal audits, and ensure that critical industry regulations are met in real time. Qualtrax is a valuable resource in highly-regulated industries where compliance with standards such as ISO 17025 and 17020, 13485 and 9001, TNI and GFSI, FDA and FQS are required.

All-in-One LIMS, ELN, QMS, and DMS Platform Xybion LIMS is an all-inclusive Digital Laboratory system including LIMS, ELN, QMS, and DMS that creates optimized workflows for the unique business needs of all regulated laboratories including research, diagnostics, quality control, stability studies, and more. Xybion LIMS instills consistency, improves data quality, and supports regulatory compliance with a complete laboratory management solution that connects with your operating systems with powerful laboratory information management and analytics.

Navigating healthcare regulatory compliance is now more manageable than ever! Compliancy Group presents its Healthcare Compliance Software, a robust solution designed specifically for the healthcare sector. Boasting an intuitive dashboard, adaptable policies, and risk evaluation capabilities, this software enhances adherence to regulations such as HIPAA, OSHA, and SOC 2. Furthermore, it seamlessly manages employee training, document organization, incident monitoring, and automatic reporting, streamlining the intricate process of healthcare compliance management.

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.

Sapio LIMS is an advanced laboratory information management system offering a unified no-code/low-code solution that streamlines laboratory workflows. Built on the Sapio Platform, which integrates LIMS, Electronic Lab Notebooks (ELN), and Scientific Data Management Systems (SDMS), it provides purpose-built solutions for scientific research and discovery, manufacturing, and clinical diagnostics. Sapio LIMS helps to optimize laboratory operations, seamlessly integrating with lab instrumentation and existing IT infrastructure. Through its robust, scalable architecture, Sapio LIMS enhances operational efficiency and ensures compliance with GxP standards such as GMP and GLP. Solutions are available for Life Sciences R&D, Clinical Diagnostics, Lab Operations and Analytics and Enterprise Data Management.

It can seem like a never-ending series of tradeoffs to bring breakthrough products to market within highly regulated industries. MasterControl's GxP software simplifies workflows, so you don't have to compromise quality for cost or innovation with regulation. Complete and connected meets flexible and fast. MasterControl Quality Excellence transforms quality data and processes to a competitive edge. Modern software is the first step in modernizing your manufacturing operations. MasterControl Manufacturing Excellence, from work orders to production records (EBR/eDHR), to logbooks and work instructions, is the easiest way to digitalize manufacturing.

iDoc is a document management system that is efficient. Automates and controls the documentation process, including distribution, organization policies and standard operating procedures. It is robust and secure in managing document management systems. It also provides real-time visibility. It streamlines all processes, including creation, review, approval, archival, and archival, and supports multiple files in controlled ways. Integration with training management system to assign training and to remove incorrect documents. This ensures accuracy for end-users and tracks compliance. Automated documentation, document retrieval with search/indexing capability, and document archive. You can easily set up labels, descriptions, and tags to help you organize information and keep track of documents. Keeps track of all documents and tracks any changes. This provides an audit trail that reports on documents and data fields.

Policy Manager's intelligent document management and workflow management software solution automates policy review, approval, and attestation across your organization. The policy management software's automated tracking features and reporting feature ensure compliance with regulatory and audit requirements. It is easy to use and simple to manage. MCN's Policy Management Software allows your staff to easily access the most recent policies and procedures through our powerful search functionality. Manager-assigned competencies track the knowledge of your staff about policies and procedures.

We are a technology and regulatory consulting company that assists businesses in implementing international standards, streamlining business processes, and accelerating global growth. Our in-house ISO consultants are available to provide expert guidance for your management system requirements. Our advisory services have been successful for many clients due to our international experience and our knowledge of companies that deal with software and hardware products in nature. No matter if you are a startup or an established company, you will find valuable features that can be tailored to your business, including setting up your QMS with all the necessary documents and maintaining it through proper document version control.

These workflows will help you create everything you need for a 510(k), and create quality records for 21 CFR Part 820 when you are ready to sell your device. Built-in tools for creating policies, procedures, or work instructions. With customized quality management reports, you can track non-conformances, deviations and CAPAs. Keep your team trained as you improve and scale your policies, workflows, and procedures. Automate validation testing for devices, apps, web and custom-made software. Reduce the time and resources required for lengthy testing, reporting, approvals, and other tasks. All your policies, procedures, artifacts can be converted into traditional documents for audit review.

CLIA requires that personnel performing waived and nonwaived testing must be assessed by your laboratory. It is a good laboratory practice to regularly assess the competency of all testers, even those who have been waived. Compass allows your lab coordinators to deliver custom competency assessments for hundreds or thousands of workers, track their completion, corrective action, as well as provide powerful reports for internal audits and accreditation audits. MediaLab's Compass allows your laboratory to eliminate the need for paper and ensure that employees comply with your competency program. Dashboards make it easy to track and see who is due when at any given time.

LabLynx offers more than standard sample tracking. It is a configurable, customizable laboratory information management system that supports inventory management, document storage and chain-of custody tracking. Our solution is tailored to meet your lab's needs. Our ELab LIMS solution redefines the concept of LIMS. It is a comprehensive information management system that can be used in every industry. This user-friendly system can be customized to meet your needs. Our LIMS Add-On Solutions will help you improve your lab's efficiency. Our solutions improve the LIMS experience and help you achieve your goals.

It is important to have a well-defined document control procedure. This will ensure that your projects run smoothly and are completed on time. It is possible to embed the document control procedure in a project document management system. This will ensure that all project team members follow the process from document preparation, approval, distribution, and then on to quality and consistent output for your client. A document control procedure for engineering drawings should include important information like the document's owner and numbering system, revision, and reviewers/approvers. You can ensure that all these attributes are in place before the publication.

Dynamically modify and manage Policies and Procedures (PnPs) dynamically. Search electronic for PnPs or agency standards. Attach notes, documents, and PnPs to the appropriate agency standard. Prepare and manage facility documents to be used in Surveys. The end-user can search agency standards electronically and view and/or attach insight, notes, operational documents, polices & procedures, and other related documents. End-users will be able to search standards, operational papers, and policies & procedures using keyword or name search functions. The end-user will be able to navigate agency surveys using step-by-step preparation tools that include amendments, PnPs, and tracking deficiency. Log-ins can also be created to allow monitoring and consulting roles. HOTB's proprietary technology allows policies and procedures to be dynamically created based on system data inputs specific for the agency.

You can use simple approvals or more complex workflows to assign approvers for your documents. This will ensure that the content is reviewed, approved, and signed off. When you use our Quality Management System workflow, you can combine electronic signatures and approvals. You can use the read confirmations feature for users to read pages and to track acknowledgments. Appfire features many top-selling apps that can help teams solve big problems worldwide. Choose from three distinct Comalatech-created workflows. You can view approved documents or review those that are pending approval.

FormFox provides industry-leading workplace safety and health tools and technology to all employers, collectors, TPAs, MROs, and laboratories. Our web-based, software-driven service streamlines all collection and event processes, from initial order to final decision, and reporting. FormFox reduces errors, saves time and expedites data delivery, improving quality, accuracy, speed, efficiency, and productivity for our clients and the people they serve.

Under the leadership of Locasoft founder, LIMS.FR was the first 100% Web French-language LIMS launched in Europe and North America in 2006. In February 2020, the Locasoft team joined LiMSEO to continue and develop its LIMS Web activity. Through close collaboration with all actors involved in laboratories (quality manger, lab manager, etc. LiMSEO has a deep understanding of the needs and operations of laboratories thanks to close collaboration with auditors, government officials and regulations inspectors. LiMSEO has close relationships with laboratories in order to better understand their challenges and needs. Our solution specialists will assist you with your IT projects. Our multidisciplinary team, which includes IT developers with lab experience, will work closely with you to ensure you get the solution you need.

Document Automation & Contract Assembly, Smart Workflows and Approvals & Document Management; Advanced Electronic Signature. Legito, your Smart Document Workspace, combines all these features under one roof. You can automate documents that are almost as easy to draft in less than two hours with Legito, your Smart Document Workspace. Legito is used by over 140,000 users from 50 countries, including top-tier law firms and companies, such as Price Waterhouse Coopers and Skoda Auto.

Document Locator is a Windows-integrated document management program that can be accessed via the Web or mobile. It combines enterprise-class capabilities with ease of use. Document Locator is fully integrated into Microsoft Windows, Office and Outlook. It offers version control, approvals, security policies, workflow, security, security, and security. All this while using the familiar Windows folders interface. This system is ideal to file HR, Accounting, Projects and Contracts, as well as Quality. Integration with other systems is possible via an advanced API.

DocControl is a web-based document control and management system. It is responsive and intuitive, making it easy to use on any device. Multiple users can work together, offering services such as large storage, versioning, electronic signatures, and automatic PDF conversion. Control is HIPPA- and 21 CFR Part 11 compliant, making it more secure than any other document manager system. DocControl can handle any type of document. It will convert it into PDF automatically. It features a great workflow for document revision. Every time a document is modified, its version number is automatically updated. Control is suitable for small to medium-sized businesses that provide security for their documents and work in a team. Control has more than 50 corporate clients, more than 5000 documents added to the system and more than 33,000 PDFs generated.

LabVantage is a platform that combines laboratory information management system, electronic lab notebook (ELN), lab execution (LES), and scientific database management system (SDMS). It allows labs to be productive and efficient. LabVantage can be deployed intelligently via a zero-footprint web browser-based interface. It is available for all sizes of enterprises as pre-packaged solutions to specific industries and via on-premise or cloud-hosted SaaS implementations. Our solutions are designed to help lab managers, scientists, technicians, and researchers better manage everything, from instruments and materials to reports and regulatory compliance to data integrity.

MediaLab's Inspection Proof module allows laboratories to be ready for inspection at all times. Uploading checklists and responding in the web-based portal means there is no need to keep track of paper or other documents. MediaLab's experts have years of experience in inspection. We have the features you need to make your inspections run more smoothly and efficiently. InspectionProof will eliminate the need for binders full of outdated policies, checklists, and standards. InspectionProof digitizes all your checklists and standards, and stores your evidence and responses in the cloud. Upload attachments, link policies and procedures in Document Control, or your own document management software, and more. Checklists can be imported from a variety of accrediting agencies, including CAP or ASHI. InspectionProof can import Excel and CSV checklists from nearly all laboratory accreditation organizations.

Qualis document management system ensures secure documentation and controlled distribution to end users. It allows workflow-based approval of documents with revision control. End users are able to access the most recent approved version of any document, reducing the risk for obsolete documentation. Roles can be used to configure the activity workflow. Multiple workflows can be set up to associate with each type of document. Reduce paper, storage space, secure storage and recovery. Distribution of approved documentation, lower risk of outdated copies. Controlled access and easy search, improved regulatory compliance. All metadata is stored in one central database. Database agnostic (supports MS SQL and Oracle, Postgre SQL). Document management at the organization level and controlled distribution. Qualis DMS provides integrated document management and control through a single platform.

Protect sensitive documents with an invisible fingerprint to prevent them being exposed to the public while printing, taking photos or snapping pictures. You can track leak source in seconds. LeaksID, a cloud-based tool, is built on a unique algorithm. Once you wish to share your document securely with third parties, it allows you to add an invisible markup. You can identify the person responsible if you have a printout, a photograph or a snapshot of a confidential document that has been made public. If you share your personal documents or data with someone, you can't guess who it was, especially if they are close friends or family. Even if you have password-protected PDFs and set enough user permissions, anyone could take a picture of your friend's screen as they pass by. LeaksID allows you to continue working as before but have more control over the document workflow and can identify the leak source quickly and accurately.

Document generation using customizable templates allows you to automate and digitize processes within your company. Maintain templates with dynamic content and standardize data fields across documents. Templates are useful for building workflows, standardizing processes, and standardizing cross-business data. You can eliminate the need to maintain hundreds upon hundreds of different document types for different product categories. Create business workflows that span multiple document types using searchable and indexed metadata. DigiDocs integrates well with DigiSign. This allows you to create a standard document, prefill it with relevant information, and have it digitally signed or electronically signed by multiple people.

Electronic signature with legal validity. Electronic signatures for your company offer security, trust, and the ability to send, approve, and sign electronically. Step by step, electronic documents Reduce the complexity of your processes Sending documents forgo the paper Send documents electronically by uploading your PDF or.docx file (Word). List the email addresses of signatories to collect their signatures 100% digitally. Electronic signature Each signer will receive a unique link to sign and save the document. You can subscribe by computer, tablet, or cell phone. It's simple and practical. Manage documents. After completion, the document will be encrypted in your account. You can save or export the document. Sign and go! Commercial contracts. Opening a loan account. General documents. Insurance proposals. School enrollment. API for integrations Use Clicksign's REST API to integrate electronic signatures into your systems and automate your signature processes.

Greenbox is an innovative document management system that combines a business process management system with a unique document management system. It is a Document Management System which allows for the storage, tracking, retrieval, and management of documents. Anybody with permission can access any file, regardless of where it is located. The system ensures complete confidentiality and safety of the documents and is designed for simplifying otherwise complex operations. Greenbox gives the user access to many features, including unlimited folders and subfolders and Solr OCR/text searching inside an image, document restoration, document versioning, granular access control, and advanced document control. Its most notable features include document approval workflow, intelligent handling of metadata, and an attractive pricing bracket.

If you are finding that outdated pen-and-paper methods of signing contracts and documents are not meeting modern requirements of your business or its customers, it is time to move digital. SigniFlow's digital signature security ensures that every document signed with SigniFlow contains the appropriate embedments to increase non-repudiation. SigniFlow can be deployed on-premise in your data center or you can take advantage of our compliant, secured datacentre offerings, which are available across all regions. SigniFlow uses the most recent cryptographic digital signature standards to secure sign PDF documents, as electronic signatures are not sufficient. Join the millions of people worldwide who are moving to digital signatures.

Docusoft collaborates with financial professionals to develop software and create innovative solutions. We address issues such as document management, cloud file storage and client data management, workflow processes and data protection. File sharing, document delivery, electronic signatures, and file sharing are just some of the many areas we address. We work together to create the best software solutions possible for accountants, insolvency professionals, financial and business advisors, and other professional service businesses around the world. Every transaction or business communication results in the creation or modification of files and documents. Docusoft CloudFiler is the best cloud document management tool to manage your business communications. Users can search, retrieve, create, automate, and process business documents from any web browser. OCR search features are also available to review documents.

Ensure patient safety and employee safety with seamless compliance and operational tools in the healthcare sector. Compliance with policies and procedures will play an important role in the new norm. SCT/CoreCompli can ensure patient safety and trust. Our digital SaaS platform offers digital and dynamic policies, and the ability to capture electronic logs using our operational tools. This will allow you to eliminate compliance deficiencies. You can have confidence in your business operations. Our compliance solutions help organizations reduce risk and increase productivity. Our applications enhance business performance and outcomes by strengthening risk management, regulatory compliance and audit/accreditation governance. Background screening administration is also available for hundreds of thousands of users across a wide range of industries. The HOTB software applications enable information security and governance professionals regain control over their data.

Zapendo offers enterprise-level features for Contract Management, and eSignature as a self service platform that any company can afford. All businesses deal with contracts, large and small. Zapendo can help you locate your contracts quickly, find out when they expire and identify the key stakeholders. You can create custom workflows to allow you to set up your approval process for every contract, task, deliverable, and company you create in Zapendo. Each plan includes unlimited eSignature features. All signed documents can be attached one- or multiple contracts.

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.

A platform for eReg that was designed with the study site in view. No forced workflow, easy implementation, intuitive design, and functional function. RegisterDoc eSafe today for free! Secure lock-box for source documents. Tools that allow remote access to sensitive documents to be transferred, redacted, and assigned roles-based, time-limited access. RegDoc eSafe allows for quick, flexible configuration and intuitive use, with minimal training and a simplified validation process. You can quickly get your clinical study sites up-and-running with a simplified implementation process. Pre-loaded regulatory binder templates for your site. Configuration of access control and user upload. Sessions for admin and user training. MedPoint is committed compliance and will walk you through the steps to validate our software. MedPoint is regularly audited and supported by study sponsors.

A scalable, real-time, collaborative, out-of-the box solution for CROs, Life Science Consultants and Industry Stakeholders. Built in an Audit Ready Compliant Cloud environment (ARCC). All 21 CFR Part 11 requirements are met. GxP audit ready. Pre-configured Departmental. Communications with internal and external stakeholder. Secure data integration between remote teams. Collaboration in review and approval. Turn access on/off according to need (EX: auditors), reducing audit prep time from days to hours. Preconfigured to eTMF Reference models & EDM. Intelligent content management tools can improve workflows. Improve document management with real-time collaboration, automatic indexing and co-authoring. Pre-configured, validated system that manages documents and data electronically in accordance with eCTD mandates.

All your governance, compliance and risk documents in one place. You can upload and share PDFs, Office documents, images, and many other files. It's easy to manage your files with automatic version control. No more searching through network folders or inboxes. Other useful features include: - Reminders for document expiry Unlimited Permissioned Users - Custom document tagging - In system notifications You can have reliable and secure visibility. It is not enough to have the most recent version of a document. To prove compliance, version control and user access tracking are crucial. TrackMyRisks offers the following: - User activity log Backup and virus scan Document revision history - Encryption all files

Xeditor is an online professional XML editor that allows you to create XML documents using state-of-the art web standards. Xeditor allows authors to collaborate on structured content from anywhere at any time. This helps companies create efficient workflows. Xeditor's web-based architecture eliminates the need for costly local installations. Xeditor, an online professional XML authoring tool, provides users with the tools they need for creating and editing structured documents in XML format. XML allows content to be created media-independently, semantically marked up and automatically processed. XML is the data format for the future. Xeditor provides both a visual and technical writing experience. The intuitive user interface of Xeditor's visual XML editor includes WYSIWYG functionality. This is a great tool for authors of subject-specific content.

The IVFID System is a security solution that was designed specifically for IVF clinics. It ensures the exact matching and verification of sperm and oocyte samples during the IVF treatment. It uses Radio Frequency Identification technology to track and verify samples at each stage, including sperm collection, oocyte tracking, Intracytoplasmic sperm Injection (ICSI), and embryo transfer. At the start of treatment, patients receive RFID-enabled wristbands. All consumables such as test tubes, cryotopes and cryotopes are marked with RFID tags that contain patient and spouse numbers and names. The system wirelessly verifies every procedure in the operating room and laboratory, recording all operational information including the procedure name and personnel involved. It also records the date and time and the specific location. The system locks itself in the event of a mismatch between the sample and the test.

Many countries require that businesses and organizations provide accessible documents that are UA-compliant to their customers. Consist's advanced accessible system solution, NAGIX, transforms large volumes of documents into fully-accessible PDFs. It conforms to all regulations regarding the rights of people with vision impairments. These documents include customer forms, financial reports from publicly traded companies, public protocols of government and municipalities, and other documents. Leading banks and other organizations use NAGIX's proven technology. Consist, a global software solutions group, has been in operation since 1972 and has extensive knowledge and experience in the implementation of advanced system solutions. NAGIX uses a powerful and innovative automatic accessibility technology that allows visually impaired customers to instantly produce an accessible version of any document.

Digitize your processes. Security. Environment. Qualitative. Hygiene. Of Business. Centralize. Simplify. Automate. All your tasks can be managed with one tool. Your organization's sustainability and performance. Automated processes are the foundation of safety and performance. BlueKanGo is the digital EHSQ platform to manage them. BlueKanGo is the digital EHSQ solution that has been trusted by over 3500 customers for 18 years. Digitize your Quality, EHS, and other processes. Quality and audits management. Employee safety and health. Environment. CMMS & inspection. Certification, Standards. Corporate Social Responsibility (CSR). Regulatory Watch. Strategic Planning. 6 key differences that make BlueKanGo different. BlueKanGo has been around for 18 years and is the SaaS platform with no boundaries. BlueKanGo is an innovative, scalable, and all-inclusive solution

Ensure seamless data integration and top-notch informatics management. iLES is a single-stop communication, documentation storage, and workflow hub for your entire organization. It works in real time. iLES supports LIMS (Lab Information System), ELN(Electronic Lab Notebook), SDMS [Scientific Data Management System] and DMS (Data Management System). Regardless of which digital stage your lab is at or what system it is replacing, iLES uses vendor neutral technologies to integrate your data. To manage all communications and lab needs, you will only need one system, iLES. Automated upgrades and rapid feature release. Access information securely from anywhere on the planet using any device that has an Internet connection. Technology that is vendor-neutral helps transform laboratories into paperless, tightly integrated environments.

Vault QMS ensures quality and compliance to GxP. Vault QMS integrates best practices and automates workflows to bring all parties - pharma, biotech companies, contract manufactures, and suppliers - into quality control processes for better visibility and control. You can easily bring departments, sites and suppliers, contract manufacturers, contract testing labs, or other partners into continuous quality improvement. Automated workflows and best practices will increase operational efficiency. Unified risk management can improve visibility across products and processes. A unified suite quality applications will improve speed, efficiency, compliance, and GxP. You can easily enable quality management processes by incorporating best practices for deviations, internal and external audits and complaints, as well as change control, CAPA and quality risk management.

Enterprise File Fabric™, a private, secure, policy driven multi-cloud content and collaboration platform, provides an efficient, secure, and private solution for storing, sharing, and collaborating with other users. It doesn't ship with storage. It works with any company's existing storage portfolio, on-cloud or off-premises. Enterprise File Fabric™, unifies, secures, and makes all types of storage (including object storage), easily accessible for end-users. The Enterprise File Fabric for Compliance is available in three product variations: 1. It enforces GDPR/CCPA/ HIPAA by providing intelligent policy-based enforcement across all corporate data. 2. The Enterprise File Fabric for Media and Entertainment provides a unified view to media assets that can both be distributed on-cloud and on premises.

LabSpeed™, Results Analysis software allows you to share, chart, report, export, monitor, validate, share, and analyze results from all types of instruments in a laboratory. These instruments can be hand-held devices, multi-element analysis spectrumrometers, bio-tech instruments, or handheld devices. You can access your instrument data instantly with minimal or no setup. LabSpeed automatically handles data connections and formats. It is easy to quickly create the solutions that a laboratory needs on a daily basis in a drag-and-drop interface. LabSpeed can simultaneously work with data from any type of analytical instrument, regardless of its complexity. LabSpeed can be used at the instrument to review, export and print data, or in the office for advanced publishing, research, data analysis, and data analysis. LabSpeed offers advanced capabilities and features that are not available in other software packages like Crystal Reports®, SigmaPlot® or InfinityQS®.