Alternatives to MediaLab Document Control

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.

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

SciNote is the top-rated platform among researchers in industry and academia. SciNote has been chosen by many of the top executive departments in the United States as their solution. SciNote allows you to organize your data however you want. It gives structure and context for all your notes, excel spreadsheets, tables, checklists, or pictures. It also includes lab inventory, compliance, & team management tools SciNote users save an average of 9 hours per week. Data research: 90% faster thanks to the fast search of all data. Reporting is 90% faster with SciNote's automatic generation of project reports. Templates: 80% faster replication of processes, experiments, and more with templates. Without SciNote, laboratory notebook tasks take 37 minutes to complete (experiment execution and some results). Type in your keyword, and SciNote will search all your projects, files, experiments and their contents. SciNote allows you to tag, notify and post comments to your team members, speeding up lab management and correspondence.

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.

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.

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.

Labguru, a cloud-based Electronic Lab Notebook, LIMS and Informatics Platform that offers a complete solution to life science research and industry, is secure and reliable. It records and manages laboratory data, inventory, molecular biology tools, and chemistry tools. This allows labs to run more efficiently and automates lab operations. Labguru allows scientists to design experiments and workflows. They can also capture structured and unstructured information, manage projects, and share their results. You can create custom-designed experiment templates and integrate protocols, SOPs and other cutting-edge features to improve data quality, streamline workflows, and reduce costs. Labguru is available via the cloud on desktops as well as mobile devices. Labguru is part Holtzbrinck Publishing Group. It serves more than 100,000 scientists from universities, research institutes, startups, and large pharma companies around the world.

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.

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.

Founded in 2006 by the visionary leader of Locasoft, LIMS.FR stands as the pioneering 100% Web French LIMS available in Europe and North America. In February 2020, the dedicated Locasoft team integrated into LiMSEO to continue and enhance the development of their web-based LIMS. Through a collaborative approach involving all stakeholders in laboratory environments—including quality managers, lab directors, auditors, government representatives, and regulatory inspectors—LiMSEO has cultivated a deep understanding of laboratory operations and their specific requirements. To ensure a thorough grasp of client needs and challenges, LiMSEO fosters strong partnerships with laboratories. Our IT project specialists are ready to assist you every step of the way, while our diverse team, experienced in laboratory settings, collaborates closely with IT developers to guarantee that we deliver the precise solutions you require. This commitment to collaboration and innovation positions us to effectively meet the evolving demands of the laboratory sector.

Sapio Sciences delivers a cutting-edge AI-driven lab informatics platform that integrates Laboratory Information Management Systems (LIMS), Electronic Lab Notebooks (ELN), and a Scientific Data Cloud into one seamless ecosystem. It is tailored to advance scientific research, clinical diagnostics, drug discovery, and manufacturing through configurable, no-code solutions. The Sapio LIMS® automates complex workflows with full configurability, removing the need for programming. Sapio ELN® offers a flexible, adaptable electronic lab notebook that supports diverse experimental needs. The platform’s Scientific Data Cloud consolidates instrument and research data enterprise-wide, paving the way for AI-driven insights. By unifying these components, Sapio simplifies data management and boosts productivity across the lab lifecycle. The platform is accessible for a wide range of industries and research applications. It aims to reduce administrative burden and enhance collaboration within scientific teams.

Laboratories that strive for high productivity and efficiency rely on the LabVantage platform, which integrates a laboratory information management system (LIMS), an electronic lab notebook (ELN), a lab execution system (LES), and a scientific data management system (SDMS) into one cohesive solution. This innovative platform is skillfully implemented through a zero-footprint, web browser-based interface, making it accessible for organizations of any scale, with tailored packages for various industries, as well as options for on-premise, cloud-hosted, or SaaS deployment. LabVantage empowers lab managers, scientists, and technicians to optimize the management of all aspects of their work, including instruments, materials, experiments, reports, regulatory compliance, and data integrity. As a prominent player in the field of enterprise laboratory software, LabVantage Solutions is committed to enhancing customer success by converting data into actionable insights that drive laboratory performance. By leveraging this comprehensive system, labs can achieve greater efficiency and accuracy in their operations, ultimately leading to improved research outcomes.

ZONTAL stands out as a prominent provider of digital solutions tailored for the life sciences sector, focusing on optimizing laboratory workflows and speeding up research results through advanced analytics and data science. Their all-encompassing platform features a range of products aimed at improving data management, including the Digital Lab for connecting experts and data, Data Preservation for the protection of critical information, and the Life Science Analytics Platform for seamless integration of analytics into laboratory processes. By prioritizing data to be Findable, Accessible, Interoperable, and Reusable (FAIR), ZONTAL enables organizations to reduce the complexities of data handling, conduct real-time analyses, and tap into limitless analytical capabilities. This transformation not only enhances laboratory operations but also promotes innovation within the modern digital landscape, ensuring that organizations remain competitive and forward-thinking in their research endeavors.

To facilitate efficient operations and timely progress in your projects, it is crucial to implement a well-defined document control procedure that enhances the flow of information. Integrating this document control process within a project document management system ensures that every team member follows the established guidelines, from document creation to approval and distribution, ultimately leading to improved quality and consistency in deliverables for clients. Typically, a document control procedure for engineering drawings, which encompass technical documentation, should also include key details such as the document owner's information, a numbering system, revision history, and the identities of reviewers and approvers. Utilizing a document control tool enables you to verify that all these essential elements are addressed prior to publication, ensuring that the information remains accurate and easily accessible. This approach not only streamlines operations but also fosters accountability among team members throughout the project lifecycle.

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.

Achieve seamless data integration and exceptional informatics management with iLES, a comprehensive hub for communication, documentation, storage, and workflow that operates in real time for your entire organization. iLES combines the functionalities of a Lab Information System (LIMS), Electronic Lab Notebook (ELN), Scientific Data Management System (SDMS), and Data Management System (DMS) into one solution. Regardless of your lab's current digital stage or which system you're considering replacing, iLES employs vendor-neutral technologies to unify your disparate data sources. This means you will only need to work within the iLES platform to manage all lab-related tasks and communications for every user. With rapid feature releases and automated upgrades, you can enjoy the benefits of the latest advancements effortlessly. Additionally, iLES provides secure access to your information from anywhere in the world on any device with an internet connection, transforming laboratories into efficient, fully integrated paperless environments. This all-in-one approach not only streamlines operations but also enhances collaboration and productivity across your organization.

LabSpeed™ Results Analysis software offers a unified platform for charting, reporting, exporting, monitoring, validating, sharing, and analyzing results from various laboratory instruments, ranging from portable devices to sophisticated multi-element analysis spectrometers and biotechnology tools. Users can quickly access their instrument data with minimal setup, as LabSpeed automatically manages data formats and connections. The software features an intuitive drag-and-drop interface, allowing laboratories to effortlessly create the necessary solutions for daily operations to enhance efficiency. LabSpeed is compatible with data from all kinds of analytical instruments, regardless of their complexity or type. It can be utilized at the instrument for tasks such as data review, exporting, and printing, or in an office setting for research, data analysis, and comprehensive publishing. Moreover, LabSpeed incorporates advanced functionalities and features typically found in separate software packages, including Crystal Reports®, SigmaPlot®, and InfinityQS®, thereby streamlining workflows and enhancing productivity across various laboratory environments. This comprehensive tool is designed to adapt to the changing needs of laboratories, ensuring that users can maintain high standards of accuracy and efficiency in their data management processes.

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.

Utilize either straightforward approvals or more sophisticated workflows to designate approvers for your documents, guaranteeing that the material undergoes thorough review and sanctioning. When integrated with our Quality Management System workflow, approvals can be paired with electronic signatures for added efficiency. Additionally, the read confirmations feature allows for the assignment of users to review a specific page while monitoring their acknowledgments. The Appfire platform boasts an array of popular applications that assist teams around the globe in tackling significant challenges. Choose from three distinct workflows designed by Comalatech, and easily access both approved documents and those awaiting approval. For users desiring greater flexibility in their approval processes, Comala Document Management provides unlimited, fully customizable approval workflows to fit unique needs. To prevent any technical complications, it is advisable not to install this app on the same server as either Comala Document Management or Comala Document Approval, ensuring a smoother operational experience. In this way, organizations can streamline their document handling processes while maintaining strict quality control.

FormFox provides top-tier tools and technology for workplace health and safety, making them accessible to collectors, laboratories, TPAs, MROs, and employers alike. By utilizing purposeful automation, our web-based software optimizes the entire process from the moment an order is placed to the final reporting and decisions made. This approach not only minimizes errors but also saves valuable time and accelerates data delivery, enhancing quality, accuracy, speed, and efficiency for our partners and their clients. The FormFox MRO solution ensures quicker results adjudication and turnaround times, implementing more streamlined workflows for the review process. Our industry-wide "Common Platform" strategy has been widely accepted, enabling laboratories to significantly cut costs while simultaneously improving the quality and reliability of testing. Furthermore, FormFox stands out as the premier Electronic Custody and Control (ECCF) solution available to all clinics within the employee health and safety sector, reinforcing our commitment to excellence in safety practices. Ultimately, our innovative solutions are designed to adapt to the evolving needs of the industry, ensuring that our clients remain at the forefront of health and safety standards.

DocControl is an online system for managing and controlling documents effectively. Its user-friendly and adaptable interface ensures that it can be utilized seamlessly across various devices. This platform enables collaborative teamwork, offering extensive features such as ample storage, document versioning, electronic signatures, and automatic conversion to PDF format. Moreover, it complies with HIPAA regulations and 21 CFR Part 11, enhancing its security compared to other document management solutions. Users can upload any document type, which will be instantly converted to PDF, while its efficient workflow streamlines the revision process by automatically updating version numbers with each change. This system is particularly beneficial for small to medium-sized businesses that prioritize document security and collaborative efforts. With a growing client base of over 50 corporate clients, DocControl has successfully processed more than 5,000 documents and generated upwards of 30,000 PDFs, showcasing its reliability and efficiency in document management. It stands out as a comprehensive solution tailored for businesses looking to enhance their document handling capabilities.

Workflows are specifically developed to assist you in preparing all necessary components for a 510(k) submission, while also ensuring compliance with the quality record requirements set forth in 21 CFR Part 820 as you prepare to market your device. These workflows come equipped with tools to facilitate the drafting of essential policies, procedures, and work instructions. Furthermore, you can monitor non-conformances, deviations, and CAPAs through tailored quality management reports. As your processes evolve and enhance, you can ensure your team receives automatic training updates. The system also automates validation testing for devices, applications, websites, and custom software tailored to your business needs. This automation significantly reduces the time and resources that would otherwise be consumed by extensive testing, reporting, and approval processes. Additionally, you can compile all your policies, procedures, and artifacts into standard documents, making them readily available for audit evaluations. Overall, this solution streamlines the compliance and validation processes, thereby enhancing operational efficiency.

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.

As a regulatory consultancy and technology firm, we assist businesses in adopting international standards, optimizing their internal processes, and promoting rapid expansion on a global scale. Our dedicated team of ISO consultants is equipped to offer reliable advice tailored to meet your management systems needs. With our extensive international experience and a strong background in both hardware and software sectors, we have successfully supported a diverse range of clients. Whether you need to establish a Quality Management System (QMS) with comprehensive documentation or ensure its ongoing effectiveness through efficient document management and automated workflows, we provide essential solutions customized for your unique organizational requirements, catering to both emerging enterprises and well-established businesses. Additionally, our commitment to continuous improvement means we stay updated on industry trends to further enhance your operational efficiency.

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.

MediaLab's Compliance & CE solution provides a complete learning management system (LMS), for your laboratory. MediaLab is a trusted industry source for over 4,000 laboratories due to its long-standing reputation as a leader in providing quality continuing education and compliance courses. Our cloud-based LMS is affordable and easy to use. We offer the tools to create, deliver, track, and track safety, compliance, continuing education that is approved by P.A.C.E., as well as custom courses to meet all your laboratory's needs.

Scispot delivers a powerful lab informatics platform that transforms how life science labs operate. Through its configurable LabOS™ ecosystem, teams can select from a unified suite of tools covering ELN, LIMS, SDMS, QMS, and AI capabilities—all accessible through an intuitive no-code interface. Purpose-built for CROs, Diagnostic Labs, and Biotech R&D teams, Scispot addresses critical challenges in Sample Management, Freezer Management, and GxP Compliance. The platform seamlessly connects with 200+ lab instruments and 7,000+ applications, eliminating manual data entry while ensuring regulatory adherence. Scispot's AI-powered analytics convert experimental data into actionable insights, accelerating discovery timelines. With rapid implementation and a focus on user experience, Scispot enables 1000+ lab scientists and operators to standardize processes, maintain compliance, and focus resources on innovation rather than administrative overhead.

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.

Streamline your document workflows to eliminate inefficiencies that consume valuable time and resources, hindering your growth and ability to secure new studies. Florence eBinders seamlessly connects all your clinical trial systems, automates eRegulatory tasks, shortens contract negotiation duration, monitors study advancement, and facilitates secure remote oversight on a leading eRegulatory, eISF, and eSource platform. With our highly-rated implementation and support teams, your team and study can be set up quickly, ensuring a smooth transition for all users. Most sites become fully operational within just four weeks! By enabling secure access for your monitors and providing remote capabilities for your team, you can significantly decrease the time spent on-site during monitoring visits. Additionally, this approach fosters a more efficient and flexible research environment.

An electronic signature that holds legal weight offers a secure, trustworthy, and convenient method for your business to send, approve, and sign digital documents. By streamlining your document processes, you can eliminate the need for paper entirely. Simply upload your PDF or .docx file and input the email addresses of the individuals who need to sign. Each signatory will receive a personalized link to provide their signature, ensuring a fully digital experience. This service can be accessed effortlessly from a computer, smartphone, or tablet, making it both user-friendly and efficient. Once the signing is complete, the document is safely encrypted within your account, allowing you to choose whether to save or export it as needed. There's no need for a digital certificate; just sign and proceed. This solution is suitable for various applications including commercial contracts, loan agreements, account openings, general documentation, insurance proposals, and school enrollments. Additionally, you can seamlessly integrate the electronic signature feature into your existing systems through Clicksign's REST API, which helps automate your signature workflows, enhancing productivity further. Embrace the future of document management and streamline your operations today.

The Qualis document management system offers a secure method for managing documentation while allowing for regulated distribution to end-users. It features a workflow-driven document approval process that includes revision tracking, ensuring that end users always have access to the most current approved document, thereby minimizing the chance of using outdated materials. The workflow can be tailored to specific roles, accommodating various organizational needs, and multiple workflows can be implemented to correspond with different document types. This system not only helps in conserving paper and storage space but also ensures secure storage and easy recovery of documents. By distributing only approved documentation, it significantly lowers the risk of circulating outdated copies. Additionally, it enhances regulatory compliance by providing controlled access and facilitating straightforward search capabilities. All metadata is stored in a centralized database, which is flexible and supports various database systems, including MS SQL, Oracle, and Postgre SQL. Overall, Qualis DMS serves as a comprehensive solution for organization-wide document management and regulated distribution, streamlining the entire process for better efficiency and compliance. Ultimately, it establishes a unified platform that integrates all aspects of document management and oversight.

Streamline and digitalize organizational workflows by utilizing customizable templates for document creation. Ensure that templates feature dynamic content and maintain consistency in data fields throughout various documents. Focus on template management, workflow construction, and the standardization of processes and data across multiple business functions. This approach drastically reduces the necessity of handling numerous document formats that cater to different product lines. Facilitate the development of business workflows that incorporate various document types while also ensuring that they are equipped with searchable and indexed metadata. With DigiDocs' seamless integration with DigiSign, you can effortlessly create a standardized document, auto-fill it with pertinent information, and obtain digital or electronic signatures from several parties involved. As a result, this system not only enhances operational efficiency but also promotes collaboration among stakeholders.

Managing data from various laboratory systems can complicate the retrieval of essential information needed to enhance operational efficiency, often resulting in disjointed workflows. Imagine the potential if you could consolidate information from nearly any laboratory information system, analyzer, or automation setup throughout your organization. Check out the video to discover how this can be achieved. With AlinIQ AMS, Abbott's analyzer management system, you have the ability to harmonize IT and workflow processes across your entire laboratory network. AlinIQ AMS offers an open, scalable solution capable of linking almost any analyzer or automation system to your LIS, facilitating improved data management throughout your operations. By leveraging five distinct functional categories alongside expert guidance, AlinIQ AMS not only boosts your operational efficiency but also enhances the quality of your laboratory information system, ultimately transforming how your lab operates. This innovative approach promises to streamline your processes and improve overall productivity.

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.

SciCord Solution features are designed to help your company transition quickly into the digital age. SciCord ELN/LIMS can be used to ensure compliance in both manufacturing and laboratory settings. Validated formulas can improve compliance and eliminate errors in calculation. To ensure compliance with SOPs, create lists. Automatic entry verification to flag possible Out-Of-Specification scenarios. Restrictions to prevent the use of expired solutions and ensure that equipment is only used by trained personnel. Intelligent scans alert reviewers to potential issues such as unstable balance, precision, uncalibrated equipment, and unvalidated process. Fully compliant with CFR 21 Part11, including electronic signatures. Custom parsing of attached files extracts data and records it in SciCord experiments for additional calculations and statistical analysis.

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.

Vault QualityDocs enhances quality processes and mitigates compliance risks through automated workflows and thorough audit trails. By streamlining review and approval procedures, it ensures efficient sharing of SOPs and other GxP documents among staff and collaborators. The automation of workflows, coupled with real-time visibility into content status, empowers organizations to manage SOPs effectively, further minimizing compliance risks. Its user-friendly interface promotes higher adoption rates and operational efficiency. In addition, the system provides detailed audit trails, organized content, and robust search capabilities that greatly improve audit preparedness and inspections. Users can securely access and interact with documents via any major web browser, and if configured, can print, distribute, and monitor controlled PDF copies. The incorporation of predefined document taxonomies, metadata, and selection lists for quality, manufacturing, and validation documents not only streamlines operations but also enables organizations to swiftly embrace industry best practices, ensuring continuous improvement and compliance alignment. Thus, Vault QualityDocs stands as a pivotal tool in modern quality management.

Arxspan's Electronic Lab Notebook offers a comprehensive cloud-based platform dedicated to the management of scientific data, effectively merging chemistry and biology information into a singular cohesive system. This innovative tool is meticulously crafted to foster collaboration in research between internal teams and external collaborators. It provides streamlined support for conducting chemistry and biology experiments and workflows all within a unified cloud-based ELN. Users benefit from advanced features such as keyword and chemical searching, alongside the convenience of attachment and in-line editing for various file types, including Microsoft Office documents, images, and instrument outputs. By utilizing the secure and private Arxspan Cloud environment, organizations can avoid the high costs associated with hardware procurement, ongoing maintenance, and IT management. The platform also features seamless integration with existing legacy electronic laboratory notebook systems, allowing for easy data migration. Users are afforded the flexibility to share views and contributions at both the notebook and project levels, further enhancing collaborative efforts. Additionally, Arxspan provides customizable user role and permission hierarchies, along with workflows for experiment signing and witnessing, ensuring compliance and accountability. The inclusion of SAFE BioPharma compatibility adds multi-factor authentication capabilities, enhancing security. Furthermore, the platform supports system validation and the management of system updates, ensuring that users remain compliant with industry standards and regulations. This holistic approach makes Arxspan's Electronic Lab Notebook a powerful asset for any research organization aiming to modernize its data management practices.

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.

The purpose of the IA software is to seamlessly gather measurement results straight from the designated testing instrument, present that information to the technician, provide a variety of editing, analysis, and auditing tools, and then transmit the results to the production area or alternative laboratories. Each IA is equipped with a single driver program designed to extract data from any testing device that has an electronic output. Over the past three decades, AcquiData has compiled a comprehensive library of software driver programs suitable for nearly every materials testing instrument currently in operation. Operating within a browser environment, multiple IA programs can function simultaneously on a single PC, allowing different technicians to test various samples at the same time. At the core of the Testream®/CS system lies the Lab Server program, which manages the flow of information into and out of each laboratory within the network. This ensures that all data is processed efficiently and accurately, streamlining the entire testing workflow.

Introducing an eReg platform specifically tailored for study sites, it ensures rapid deployment without imposing rigid workflows, featuring a user-friendly design and functionality. Experience RegDoc eSafe free of charge today! This platform acts as a secure vault for source documents, equipped with tools that facilitate the transfer, redaction, and assignment of role-based, time-limited remote access to sensitive information. RegDoc eSafe boasts fast and flexible configuration options, requires minimal training for intuitive usage, and includes a comprehensive yet efficient validation process. The implementation is streamlined to quickly prepare your clinical study sites for operation. Additionally, regulatory binder templates are readily available within your site for convenient retrieval. The platform allows for user upload and access control settings, along with dedicated training sessions for both administrators and users. MedPoint prioritizes compliance, guiding you through all necessary procedures to validate our software effectively. With a wealth of experience in developing and supporting validated systems, MedPoint undergoes regular audits by study sponsors, ensuring the utmost reliability and quality in our offerings. Our commitment to continuous improvement and user satisfaction sets us apart in the industry.

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.

The SCHEMA Group, a medium-sized software company with over 130 employees, was founded in Nuremberg in 2015. The SCHEMA Group provides content delivery and component content management solutions for authoring departments that create product-related content. The SCHEMA ST4 component management system is one of most commonly used systems for modularised documentation, package inserts, and marketing documentation. The system covers all aspects of creation, revisioning, variant control and publication of product-related material - from authoring assistance during input until the final layout for the printed catalog.

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.