Alternatives to RegDocs365

isoTracker Quality Management is a popular cloud-based quality management software (QMS) system. It is used on a worldwide basis by businesses to manage their ISO 9001, ISO 13485, ISO 22000, ISO 17025, ISO 14001 systems...plus many others. It is a modular product which can be configured to meet an organization's specific requirements and is competatively priced with superg customer support. Any module combination of Document Control, Complaints, CAPA, Audits, Training, Non-Conformance and Risk can be subscribed to.

It is difficult to make data available and actionable when a manufacturing site has many processes. As operations grow, it is becoming more difficult to comply with safety, quality, and environmental regulations. Manufacturing is built on predictability and reliability. Manufacturing by nature is all in the execution of established processes. TenForce was built from the feedback of our clients to map the operational reality in a plant.

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.

UnForm is a powerful enterprise document management and process automation solution that seamlessly integrates with any application. Our platform-independent, fully browser-based solutions provide the ability to create, deliver, capture, index, route, and store documents from start to finish so that a transaction’s entire life cycle can be accessed with one easy search. Our data extraction and workflow capabilities enable the automation of data entry-intensive processes. UnForm.Cloud, a hosting service for UnForm Document Management, is a perfect fit for those who are running cloud-based ERP systems or looking for a solution with no hardware to purchase, manage, or maintain. Implementing UnForm has never been easier. Backed by a proven hosting vendor, Oracle, you have the peace of mind knowing your data is safe and secure with well-managed data centers and cross-region backups, ensuring reliable and continues access to your data when you need it.

LogicalDOC empowers organizations all over the globe to take complete control of their document management. This premier document management system (DMS), which focuses on business process automation and quick content retrieval, allows teams to create, collaborate and manage large volumes of documents. It also stores valuable company data in one central repository. The system features include drag-and-drop document uploads, forms management, optical characters recognition (OCR), duplicate detection and barcode recognition, event logs, document archiving and integrated document workflow. Schedule a free, no obligation, one-on-one demo today.

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.

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.

Document Control is MediaLab’s document management system. Our online solution empowers lab directors and supervisors to manage their policies, procedures, forms, job aids, and worksheets using configurable review settings, custom approval workflows, automated employee sign-offs, and more! Reduce time spent chasing approval and review signatures while benefiting from email notifications and personalized to-do lists for employees. MediaLab's Document Control supports: • Digital records and version control of all documents, • Standardization across all documents from all sites, • Electronic signatures that meet 21 CFR Part 11 standards, • Customized approval workflows and processes, • Robust searching to easily locate specific documents, and more!

The SBS QMS Suite consists of 5 software modules that work together for efficient Quality compliance: SBS Quality Database - CAPA / 8D corrective and preventive actions (CAR) with root cause analysis - Nonconformance management - Risk analysis including FMEA, SWOT, interested party risk register - Internal, customer, and third-party audit management - Environmental Health and Safety (EHS / HSE) management SBS Ground Control - Employee training management (LMS) - Self-Paced training - Document control SBS Asset Tracking Database - Calibrated equipment control - Preventive maintenance - Asset inventory management SBS Inspection Database - Record incoming material, in process, and final product inspection data - Generate real time SPC charts - Inspection plans and Control Plans - Archive data for further statistical analysis SBS Vendor Management - Maintain an approved vendor list or AVL - Develop vendor / supplier qualification plans - Maintain vendor / supplier qualification history Modules may be purchased separately or in any combination.

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 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

Arone has over 20 years of experience in software edition and clinical research. We offer clinical research organizations a complete suite to help with patient data entry and management. Our solutions are fully integrated and our team will provide personalized support to help you conduct your studies and projects. All patient data can be managed in one place. Arone manages randomization of patients by randomly assigning treatment options to study participants in order to eliminate bias. Participants in clinical trials can be empowered to enter their data every day. Get a tailored support for your projects.

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.

Cloudbyz eTMF is a cloud-based solution that offers a repository of all clinical trials documents, including images, files, information, etc. Store, manage, and easily share all documents related to clinical trials in a digital format. Manage trial documents, remain inspection-ready, and provide real-time visibility to CROs and sponsors, as well as monitors and other stakeholders.

LifeSphere eTMF provides a single source of truth for your clinical trial. Discover a flexible solution that streamlines the inspection process, ensures compliance and saves time and effort for your organization. LifeSphere eTMF is the first system that supports the TMF reference models. It aligns Clinical documentation, regulations and study protocol in one solution. Create and manage your clinical trial from a single source. Live collaboration and real-time sharing of documents will ensure the quality, timeliness and completeness of your trial master files. TMF inspections can be streamlined quickly and efficiently for any audit. Maintain compliance using embedded workflows and dashboards which allow easy trial reconstruction.

Collaboration and document control. myClin is an eTMF platform that allows for collaboration and collaboration. You can upload and share your study documents on myClin's secure central channels. You can access your documents quickly and receive critical updates and training faster. You have full control of your data. The "File it!" feature allows you to see who has read and understood your study materials. You can record evidence of study execution and review training actions such as views, filing or downloading at individual or team level. Inspection readiness. Always be ready for inspection. Our compliance score shows how compliant each study site or team member is with the appropriate study information. You will be guided to areas that are less compliant in your study. This helps you improve risk management. We will create a myClin channel so you can share myClin with the team in just a few hours. It's that simple.

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.

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.

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.

Nira, a real-time access control tool that allows visibility and management of who has access to company documents within Google Workspace, is called Nira. Sharing a link is all it takes to collaborate. Information about company information can be scattered among employees, departments, or external parties. Access management becomes a full-time job. Personal accounts are not scrubbed by standard offboarding processes or tools. Outsiders have access to their accounts until they are audited. Access incidents are difficult to diagnose and fix. Nira connects with your cloud applications and gives you a single view of who has access. You can control document access to both internal and external accounts. Real-time access to all documents and their risks. Quickly manage vendor access to company documents. You'll be amazed at how easy and quick it is to manage access.

Adept Software provides fast, central access to your most important documents in an environment that is secure and collaborative. This saves time, reduces risk, lowers operating costs, and lowers your business' operating costs. Your company can be aligned on a single platform that provides a single source for truth and a unified view of engineering content and business content. You can empower stakeholders from anywhere to find the right document quickly, regardless of where it is stored. This will increase productivity by 20-30%. You can avoid costly mistakes and safety concerns by making sure your workforce always finds the right version. You can improve efficiency and eliminate bottlenecks with documents that follow predefined approval procedures. Notifications and time-based notifications keep everything on track. Everyone can collaborate on the same platform and do design reviews. Vaults can easily be replicated so that documents are accessible to everyone locally. Adept also keeps everything in sync.

Learn how top financial services and wealth management companies are using FutureVault in order to meet compliance, gain back-office and admin efficiencies, deliver greater value to clients, and ultimately save time and money. You can streamline and digitize document-related workflows, reduce security risks and compliance risks, and build trust with clients and their families. You will be able to improve compliance and administrative efficiencies, as well as providing your advisors, front office teams, and lines business with a value-add offering to scale workflow.

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.

airSlate WorkFlow, the first and only no-code platform for business automation, is a holistic platform. AirSlate WorkFlow combines electronic signing, no-code robotic automation, contract negotiations, document generation, and web forms in a single business automation platform. Configure and automate every business process, and integrate it with any system of records without writing a line of code. Start any process directly from your record system with just one click. Automatically pre-fill data, route documents according to real-time updates and archive completed documents. Start in minutes by choosing from tens or thousands of pre-built document templates and workflows for any industry and department. No need to integrate multiple platforms or services. The time to value is reduced by 10x with no-code configuration and deployment.

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.

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.

Improve productivity by automating, streamlining and reporting clinical trial operations data in all study management processes. Siebel CTMS, a comprehensive and scalable integrated trial management suite, improves operational efficiency through standardizing clinical operations workflows, while providing real-time data visibility. Siebel CTMS offers trial management capabilities to help you manage and monitor your trial operations from beginning to end. Siebel CTMS can be configured for each customer's process to improve data quality. Siebel CTMS is integrated with advanced analytics that can provide you with timely and fact-based insights into clinical programs in order to drive informed decisions. You can access complete and accurate clinical trial data in real-time to make better decisions more quickly and effectively.

eDeviation supports all operations related to Protocol Deviation management and assessment. From software design and validation to gathering supporting documents and exporting data to the TMF, eDeviation®, relieves your clinical staff from the risks of missing or incorrectly assessing protocol deviations.

The premier clinical trial management system, specifically designed to overcome the technical challenges of managing clinical trials. CTMS Master makes it easier for users to communicate, reduces manual work, and eliminates redundant data and tasks. This allows for more efficient trial conduct. A Site Visit Report tool that integrates with an automated workflow eliminates duplicate data entry. It also facilitates the creation and distribution of out-of-the box Site Visit Reports (SVR). Standard templates can be used for site and project documents, budgets, events, milestones and site visit reports. CTMS Master offers more than 100 metrics/statistics to help you track clinical study sites, countries, and projects. It also includes 80+ standard reports and ad-hoc reporting capabilities. CTMS Master allows you to create site-specific budgets using a default template, track accrued and future obligations, and define automatic or manual approval for each payment type.

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.

Clinical One RTSM supports a randomization scheme for the simplest and most complex studies, without the need for programming. This eliminates the need to conduct lengthy user acceptance tests. Self-service configurations allow you to take control of your study and create a study within days, not weeks. Assess the status of drug inventory in real-time and make changes without having to contact the vendor or incurring costs and change requests. Eliminate the need for change requests and avoid delays with quick implementation of changes and promotion of your studies. The only platform to truly unify people, processes and data in order to simplify and accelerate clinical trials for the future. Virtual components in clinical trial allow for greater patient participation, and improve the quality of clinical trial data. To accelerate study start-up, we need to transform digital strategies to harmonize and streamline data from all sources.

DocShifter software automates the conversion of digital content. Our solution converts high volumes of any digital document or content (document, images, video, audio, etc.) into any other digital format. On premise or in the cloud. We serve customers in highly regulated industries: Life Sciences, Banking & Insurance and public sector. We are proud to contribute to the success of leading companies such as Bayer, Novartis, Biogen, Sanofi, Chiesi, Otsuka, Galapagos, TAI, and many others. As our world has gone fully digital, content conversion serves many purposes: From creating compliant PDF in context of the submission of a new drug, to file format preservation in archiving, to document standardization during migration. What makes us different? We make this process super easy. Setup and forget. We provide high quality conversions, at high speed. And we do all of this with limited compute power. Resulting in lower cost. We run in any environment, from Docker over Linux to Windows. And connect to all your enterprise systems. Centralizing. Reducing cost across the enterprise.

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.

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 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.

Open interfaces ("API First") allow integration of applications for almost all possible input and output channels. Consistent optimization of communication processes ensures high performance even for large document volumes. NodeJS (NPM packages), web-based APIs that are documented and customized, and customer-specific process modules allow for greater flexibility. Modification of document control processes according the customer's specifications. Your business, your rules. Our professional services team will assist you. Access to all pre-configured (partial) processes via a web service that can be called by third party solutions. DocBridge® Gear is a platform with which all processes of document creation, conversion, modification and output can be easily configured customer-specifically - independent of a specific (given) page format and based on raw data. You will find examples of quality assurance processes like document check/comparison and validation, release workflows, and so forth. Models can also be used.

Scan documents, files, photos, video, and many more. You can collect almost any media format. Facilitate the flow and security of documents from a unified repository. To improve accuracy and version control, reduce multiple copies of documents that are scattered across different systems. To improve productivity and efficiency, encourage sharing of documents within the organization. Access your documents from any device, whenever you need them and wherever you need them. Security controls, encryption, and authentication modes built-in. Search historical records using complex queries to find the information you need quickly. You can manage all your information from one place: paper scans, efiles, video. Based on configurable roles, assign access to features and document rights. Proven performance in large volume deployments, from one department to the entire enterprise.

Avvoka is an automation, negotiation, and analytics tool that helps law firms, in-house lawyers, and businesses of all sizes to create documents, negotiate them, and use data insights from that process, to draft better documents and get to "yes" quicker. Avvoka allows you to quickly create automated versions of complex documents, unlike legacy tools. This means that Word documents no longer require complicated coding. Customers can quickly reach an agreement by working with colleagues in real time and negotiating via the Avvoka online platform. Avvoka also offers sophisticated reporting tools that enable businesses to monitor pushback against standard contract clauses, track key terms commercial terms, and compare individual negotiators' performance.

Our products Xeditor & Xpublisher enable collaborative creation, full administration, and easy publishing of content across all channels. This allows for highly automated production of journals and technical documentation. Our online XML editor makes it easy to create, edit, and review structured content quickly. You can access all your XML documents from anywhere, anytime. And you can collaborate with other authors in real time, regardless of technical skill. Manage and structure your content and any additional digital assets efficiently with our online publishing system Xpublisher, for a highly automated, fast and accurate multichannel-publishing. Our products Xeditor & Xpublisher have been adopted by many leading companies. They now benefit from digitalization in multichannel publishing. We offer turnkey solutions for these problems with Xpublisher or Xeditor. This will allow you to create content quickly and publish it automatically.

KRYSTAL Document Management System, a completely web browser based Document Management System Software Solution, is provided by Primeleaf Consulting Private Limited, an Indian Company based out of Mumbai, India. It is an award-winning Document Management Software Solution from Primeleaf Consulting, Mumbai, India. It is easy to install, easy to configure and easy to use system that allows you to spend more time on customer facing activities – instead of on tedious administrative and paper-based chores.

Document management, workflow, and portal solution with integrations to accountants and tax professionals. Doc.It Suite software helps tax and accounting firms stay organized by streamlining digital processes and automating them. This increases efficiency, workflows, and profitability and minimizes risk when dealing with financial documents.

The Seismic Enablement Cloud, a comprehensive platform, is designed to improve the ability of sales, marketing and customer success teams to engage and convert their customers. It includes a variety of features, including content management, coaching tools, and sales training. This ensures that teams have access to the right resources, at the right time. Seismic's powerful analytics allow users to track engagement, optimize performance and gain insights into the effectiveness of content and team activities. The platform uses AI and machine-learning to provide personalized content suggestions and streamline workflows. This makes it easier for teams and their members to collaborate and grow revenue. Seismic unifies enablement functions to help organizations improve sales effectiveness and accelerate the buyer's experience, ultimately achieving better business outcomes.

Protect your documents from unauthorized access and limit their use. You can be more efficient, faster, more automated, and more agile. Protect customer data from wrongful disclosure and ensure secure access to business applications. Trade secrets and intellectual property can be protected. Reduce the security gap between perimeter security and user collaboration. You can monitor and protect your business-critical documents such as intellectual property or product design from anywhere it travels. This includes apps, cloud services, on-premises, and devices. SkyDRM uses dynamic authorization technology and digital rights management to protect files and allow secure sharing. The document's protection remains with it, no matter where it is stored or with whom it is shared: within or outside your network, on file server or in the cloud. You can determine whether your file is accessible, viewed, edited or printed.

ImproWise is a web-based platform that is 100% secure and HIPAA-compliant. It was designed to manage Clinical Trial Management (CTMS), and Clinical Data Management System (CDMS) from beginning to end. ImproWise combines CTMS, CDMS and EDC functionalities with unparalleled flexibility, speed and security. ImproWise was designed to meet the requirements of all stakeholders in clinical trials. Our platform is designed to ensure seamless collaboration and efficiency for everyone involved in clinical trials, from sponsors and investigators, to data managers, entry specialists, site personnel, and regulatory affairs professionals.

The digital transformation is a challenge for organizations. They need solutions to inject intelligence into their workflows including their document management and print control work streams so that they can drive business outcomes, reduce costs and impact their bottom line. Tungsten Output Manager provides the most intelligent governance to meet your document control and printing management needs. Its superior security capabilities help organizations improve document safety, minimize inefficiencies, and mitigate compliance risk. Tungsten Output Manager’s best-in class print and document controls capabilities enhance process orchestration. This includes intelligent redaction and keen rerouting, which increases workforce capacity. Tungsten Output Manager protects printed documents and prevents unauthorized information flow.

Check out our quick screening tools to help you identify high-risk patients with colorectal, breast and other cancers. Progeny Clinical makes it easy to manage family history, assess risk, and determine treatment options for your patients. You can access family history data online from your patients and create pedigrees automatically before you visit the clinic. You can edit or create new pedigrees at any time. You can instantly run validated hereditary risk assessment models for cancer at the touch of one button. Ambry Genetics offers genetic testing at a fraction of the cost. You can track and view lab results without leaving the software. Save time by creating letters, notes, reports, letters, and other documents using custom templates that include patient data fields. Quickly generate custom queries or spreadsheet reports using pre-configured data entry screens. To display the most recent pedigree, add a hyperlink to your electronic medical record.

All aspects of your clinical trial can be managed from one platform. Zapclinica, an eClinical suite, is designed to manage and execute every aspect of your hybrid or virtual decentralized clinical trial. Automate complex processes, identify outliers and optimize resources. This will improve decision making and collaboration among sponsors, CROs, sites, and other stakeholders. Zapclinica makes it easier to manage a clinical trial. All aspects of your clinical trial can be managed from one platform. Zapclinica, an eClinical suite, is designed to manage and execute every aspect of your hybrid or virtual decentralized clinical trial. Automate complex processes, identify outliers and optimize resources. This will improve decision making and collaboration among sponsors, CROs, sites, and other stakeholders. Zapclinica makes it easier to conduct a clinical trial that is successful. All aspects of your study can be covered with one platform. You can choose the app that you need in one environment, with no additional vendors or third-party.

Trialpack Designer is a powerful and easy-to-use tool that allows you to create blister packs and cards for clinical trials. It is especially useful for designing packages for complex blinded trials, such as dosage titrations and double-dummy. It contains configuration data for the Trialpack PC Controller and the Trialpack Controlled Dosing Systems. Easy and direct on-screen design of filling patterns, print images, and blister shapes. Access rights for users can be very precise. Workflow features that include electronic signatures. Audit trail that is 21 CFR Part 11 compliant. Reports with detailed packaging instructions.

iOMS For Research Teams(c), was developed in collaboration by The Royal Wolverhampton Hospitals NHS Trust. It contains a cohesive integrated set of modules that helps all stakeholders effectively manage research management areas. All stakeholders can access a single platform that provides real-time views and engages them in research. Decision making is made easier by the inclusion of drill-down and detailed reports.

Full cycle product for Research and Development Teams in the Pharmaceutical Industry. The product includes Electronic Trial Master File and Trial Management. It also has Electronic Document Management with eSignature support. This product is suitable for areas regulated by 21CFR Part 11 requirements.