Alternatives to MediaLab Document Control

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.

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.

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.

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.

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.

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

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.

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.

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.

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.

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.

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.

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.

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.

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.

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®.

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.

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.

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.

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.

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.

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.

Scispot stands as the premier technology platform for the biotech sector, offering an unparalleled toolkit designed for customization without the need for coding. Imagine a powerful blend of Electronic Lab Notebook (ELN), Laboratory Information Management System (LIMS), integrations, and analytics. This platform allows for easy setup, either through a graphical user interface (GUI) or command line interface (CLI), aimed at transforming your digital biotech ambitions into reality. With Scispot, you can craft your data infrastructure, streamline your workflows and integrations, and prepare your data for advanced applications like machine learning and artificial intelligence, all from a single platform. It also offers ready-to-use templates for key experiments, facilitating collaboration and efficient data management.

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.

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.

Inefficient document workflows can be eliminated, which can lead to a loss of time and money and a reduction in your ability to scale up and attract new research. Florence eBinders integrates your clinical trial systems, automates eRegulatory processes and tracks study progress. It also enables secure remote monitoring via the industry-standard eRegulatory and eISF platforms. Florence eBinders integrates your clinical trial systems. It automates eRegulatory processes and reduces time for contract negotiation. It also tracks study progress and allows secure remote monitoring. Our top-ranked implementation teams and support team will quickly set up your study and get all users connected. In less than four weeks, most sites are up and running. Secure access to your monitors and remote access for your team can reduce the time spent on site monitor visits.

It is difficult to find the information you need to improve efficiency because of the data stored in different laboratory systems. This can lead to fragmented processes. Imagine if you could combine data from any type of LIS, analysis, or automation system across your entire institution. You can see the video to learn how. AlinIQ AMS is Abbott's analyzer management software. It allows you to standardize IT and workflow functionality throughout your entire lab system. AlinIQ AMS can connect almost any automation system or analyzer to the LIS, allowing you to manage data flow throughout the entire process. AlinIQ AMS offers five functions and expert advisors to improve your operational efficiency.

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.

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.

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.

Arxspan's Electronic Lab Notebook, a cloud-based platform for scientific data management, combines biology and chemistry data in one system. It is designed to facilitate collaboration between internal teams and external partners. Single cloud ELN supports chemistry and biology experiments. Advanced, chemical, and keyword searching. Attachment and inline editing for all Microsoft Office, image and instrument files. The private, secure Arxspan Cloud environment allows for deployment without the need for hardware maintenance, acquisition, or IT overhead. Integration with legacy electronic laboratory notebooks systems is possible out of the box. View and/or create sharing capabilities at the notebook and project levels. Configurable permission hierarchy and user roles. Test signing and witnessing workflows. SAFE BioPharma compatibility with multi-factor capabilities. Support for system validation and system updates

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.

The IA software's role is to automatically collect measurement results from the test instruments assigned to it. It will then display this data to the tester and offer many other editing, analysis, and audit features before sending the data off to the production floor, or other testing laboratories. Each IA includes a driver program that can pull data from any instrument with an output electronic. AcquiData's extensive library of driver software programs has been developed over the last 30+ years for virtually every materials testing instrument currently in use. In the browser environment, multiple IA programs can be run simultaneously on one PC, allowing different samples to tested by different technicians at the same time. Lab Server is the heart of Testream(r/CS). The Lab Server program's main job is to control information flow into and out of the various laboratories within the system.

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.

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.

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.

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.

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.

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

The most widely used LIMS (Laboratory Information Management System) is the best way to increase productivity, ensure compliance, streamline operations, and improve organizational efficiency. Thermo Scientific's SampleManager LIMS™, which combines laboratory management, data management (SDMS), and process execution/procedural ELN(LES) capabilities, is the world's most widely used LIMS. SampleManager LIMS is used by laboratories in all industries including pharmaceutical, food, beverage, oil and natural gas, manufacturing, contract testing, and water and environmental.

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.

Streamline regulatory operations within your organization to improve compliance. Veeva SiteVault simplifies clinical trial management by connecting all regulatory operations. This improves efficiency and compliance. A single system that integrates regulatory and source documents supports 21 CFR Part 11 compliance and HIPAA requirements. SiteVault Enterprise provides real-time visibility across trials and speeds study activation. It also enables faster and more quality trial execution. To speed up study activation and reduce manual work, you can replace manual processes with your own workflows. Monitors will have secure, direct access into your source and regulatory documents. This will eliminate the need to redact or grant EMR access. You can create your own workflows, reports and dashboards to gain greater insight into regulatory processes and start-up timelines.