Alternatives to RegDesk

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.

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

The regulatory affairs departments in the healthcare and life science industry are driven to improve efficiency and create intelligent systems that optimize costs, maximize accuracy, and reduce submission times. RIMTrack, a cloud-ready, artificial intelligence (AI)-based, new age regulatory information management system, addresses this concern. It was created from scratch to assist organizations in preparing submissions accurately and efficiently. It streamlines regulatory processes related to licensing, approvals, regulatory, competitive intelligence, clinical trials and reporting across global stakeholders. Integrate with existing RIM systems to achieve complete management of the regulatory lifecycle process.

End-to-end regulatory information management from a single platform. The Vault RIM Suite streamlines global regulatory process on a single cloud-based platform. This allows life sciences companies to increase visibility, data quality, agility, and efficiency. You can respond faster to changes in regulations and improve process efficiency, from submission planning to publication. Coordinate regulatory efforts across HQ and affiliates within a single RIM platform. Assure that teams are creating reliable regulatory content with high data integrity. Veeva Vault Registrations manages product data worldwide, including variations, registration status, and interactions with health authorities. Veeva's flexible data structure supports IDMP data points, and will continue to support changing regulatory data standards. Veeva Vault Submissions automates regulatory process steps and streamlines submission planning.

Kalypso offers life sciences companies a cost-effective accelerator to implement a RIM system - Accel for RIM. The integrated platform allows for efficient product distribution and management, as well as a global platform to track and manage product registrations. It consolidates compliance data and quality data from different enterprise solutions into one global source of truth to facilitate product registrations and tracking in order to speed up regulatory submissions. Modern APIs are used to combine product data, regulatory documentation, and submission packages. Pre-configured for quick implementation with a valid software system. Based on industry-leading RIM practices.

Imagine all your regulatory information about products, registrations and submissions, correspondence, and commitments in one central place, accessible from anywhere. Ennov RIM allows life sciences companies to streamline their regulatory processes, improve data quality, quickly respond to business-critical questions, and effectively responds to health authority requests. Ennov RIM, a purpose-built application based on Ennov Process, allows for the tracking and management of therapeutic product details as well as registration information. Ennov RIM gives regulatory personnel the essential information and functionality they need to manage product portfolios globally, whether you're planning to launch a new product or handle variations to existing registrations.

All the information you need to register your IVD product or medical device in any market worldwide and manage your market access licence throughout the product's life cycle. REGISLATE®, which provides information about medical and IVD device-specific submission file requirements for each country, allows users to manage their market access licenses through the product life cycle. You can track milestones, timelines, estimated and actual completion dates, as well as estimated and actual completion dates, for initial registrations, renewals, amends, and license transfers, in real-time. For clear monitoring and management, infographic data and proprietary indicators are available. Collaboration tools are available to assist with the preparation and review submissions, compliance requirements, and documents. Receive progress reports in real time for current and future submissions, including market access readiness index. REGISLATE®, which includes GR-MAP registration tracking, for both country AND product.

ClinChoice manages global regulatory data with technology expertise, a deep understanding and best data management practices. ClinChoice uses its expertise in technology and regulatory affairs to help organizations manage their regulatory information. Our consultants offer general data maintenance support in regulatory Information Management System (RIMS) software. This will help ensure that applications are submitted, approved, renewed, and tracked on time. We offer the necessary support in managing and controlling the drug registration process. This allows drug and medical device manufacturers to track all regulatory information and has the ability to see it. Organizations can develop short-term and long-term strategies that meet submission deadlines with minimal impact on their day-to-day operations.

Global regulatory affairs system that includes registration management software and support from regulatory experts around the world. This registration system is required to renew, amend, transfer, or modify your IVD market access approval or medical device. The intuitive user interface of LICENSALE®, which includes real-time data and infographic analytics, allows for project management, collaboration, future market access planning, advanced reporting, and effective project management. It allows you to take control of your global medical technology registration activities. Arazy Group's "in-country regulatory experts" review your compliance documents and assist in the preparation of your applications. They will work with authorities until you receive your desired marketing approvals. LICENSALE®, which includes compliance and submission requirements for your product in over 140 countries, as well as regulatory experts to help you with each market.

ViSU™, a cloud-based End-to End Regulatory Information Management platform (RIM), is specifically designed for the medical device industry. It allows global users to access and manage regulatory data (Product Master and Registrations, Tracking), Dossiers/Tech files (Submission planning and building & lifecycle), HA/NB correspondence and Obligations tracking. ViSU helps you embrace digitalization in regulatory. It provides connectivity, traceability, and automation which leads to regulatory management efficiency, lower compliance risks, and cost reduction.

Rimsys provides a single, cloud platform for end-to-end regulatory process digitization and automation. Designed by and for regulatory affairs professionals, Rimsys helps medtech companies reduce repetitive administrative work, speed time to market, respond faster to changing regulations, and drive alignment across internal teams, affiliates, and partners. Only Rimsys provides a holistic platform that supports a full range of regulatory activities. Use regulatory intelligence and digital templates to guide regulatory strategy and streamline submissions. Create compliant, submission-ready content, and consolide PDF packages for electronic and print submissions. Digitally collect and maintain evidence of compliance. Link to relevant standards and get notified of changes. Get notified of changing standards, laws, regulations, and guidance documents that impact your products. Create self-service application, product, and country reports to see exactly where your products can be sold and their current registration status.

EXTEDOpulse, a comprehensive RIM software solution, consists of five hubs that address all stages of product development. You can use the applications separately or combine them to get additional value based on your needs. The development of pharmaceutical products can be complex and require input from many people. Life science organizations face many challenges due to the complexity of operating in a highly regulated industry. We are able to provide you with great synergy and connection, as well as innovation, for compliance. EXTEDOpulse was designed with these aspects in view to help you connect the dots throughout the entire lifecycle pharmaceutical products. EXTEDO is familiar with the complexities involved in the regulatory pharmaceutical product journey.

Essenvia delivers business value to all departments and teams, and increases efficiency across the board. Centralized repository of all regulatory information allowing collaborative authoring, reporting, and eliminating technical holds, RTAs and RFIs. The regulatory affairs department is empowered to accelerate product launches, and eliminate revenue losses due to delays in submissions and missed renewals. Helicopter view over the entire regulatory lifecycle. Executive dashboards, metrics and proactive alerts are available for global registrations and submissions. Essenvia, a RIM Platform, allows you to manage regulatory workflows throughout the entire product lifecycle. It also accelerates global market access and generates exponential business value. Consolidate all regulatory activities onto one platform to bring your devices faster to market. All registration documents linked to product master information are stored in a central repository. Manage the product registration lifecycle per country.

PhlexRIM dramatically improves compliance by providing you with real-time, efficient and effective access to your global registration information. PhlexRIM 2.0 includes a library of pre-configured automation "bots" and built-in regulatory use case examples based on industry best practice. The intuitive drag-and drop design tool allows regulatory teams to automate their business processes without the need for programming knowledge or IT support. Manage the entire lifecycle of pharmaceutical product registration activities. Access detailed status information and make use of the alert management feature that is part of all workflows. You can either use standard reports to illustrate your reports or create your own reports. You can create and assign regulatory tasks to your organization for management, headquarters, and affiliates.

High-cost contributors are essential for regulatory functions. They can be found in a wide range of regulatory content. This problem can be solved by a cloud-based solution like Infosys' regulated document management platform. Externalization, collaborative authoring, and editing. Simplify governance and processes; implement a consumption-based model. Support audit trails. Implement a proven solution that guarantees 99.95% uptime in production. Our solution allowed business users to search documents in a vast repository in just 3/4 seconds. Users also had unlimited storage on-demand. To reduce operational and maintenance costs, the DMS uses Google's application programming interfaces (APIs). The company's overheads are restricted to API usage and storage space.

RIMExpert™, which addresses regulatory planning, tracking, and data management, manages the global rollout plans and automates the creation of regulatory activities, medicinal products, and regulatory applications. RIMExpert™, reduces data entry requirements, improves data quality, and increases global oversight and control. Standardize regulatory planning, tracking, and registration management processes. Increase collaboration between affiliates and headquarter. All registration activities can be done in one place. One point of contact for all applications, questions, correspondence, and commitments. To maximize the efficiency of enterprise regulatory resources, sync your efforts. You can monitor registration activities throughout the product's lifecycle, keeping track of deadlines, status of commitments, and agency questions. Interactive dashboards to monitor and control regulatory activities and registrations.

Mednet is an eClinical technology company that specializes in healthcare solutions for the global life science community. Mednet's flexible, EDC-centric eClinical platform increases the efficiency of clinical research of all sizes. Mednet's comprehensive solution suite provides all the tools necessary to create and manage clinical research. It can also adapt to changing demands and requirements. Mednet has been trusted by CROs in every sector of the pharmaceutical, medical device, and biotechnology industries for almost 20 years. They provide the expertise, reliability, and innovation that they need to succeed. Mednetsolutions.com has more information.

OpenText™, a leading provider of information management solutions for life sciences organizations, helps them to harness insights from data and content to improve their decision-making and accelerate product development. Integrate, manage and securely exchange data between people, systems, and things. Use information assets to drive innovation and commercialization. Cloud-native software can run anywhere, giving you freedom of choice. OpenText for life sciences accelerates discovery by delivering actionable insights that can be used to drive innovation in pipelines. Intelligent capture allows you to capture and manage research papers in electronic lab notebooks. Text mining can help you gain insights. Unstructured text in clinical trial reports, study protocol, clinical safety and efficiency findings, can be used to extract knowledge. Learn how to intelligently analyze and classify clinical trial documents and extract them to reduce the risk for costly stops and starts.

Ennov Regulatory Suite is a world-class solution for regulatory content and information management. It is a unified, centralized and end-to-end solution that supports the regulatory information workflow, from the earliest stages through market authorization. This is a common principle that companies who strive to achieve regulatory operational excellence share. This is because they know that such a solution will allow them to drive harmonization and promote standardization, improve collaboration and ensure compliance, eliminate waste and reduce costs, accelerate product releases, and allow them operate and compete in global markets more effectively. Ennov Doc, Ennov Dossier, and Ennov Process combine to provide support for the entire regulatory product cycle, from early planning of registration targets to product retirement. The Ennov Regulatory Suite is a valuable tool for planning regulatory activity.

Protect your business, meet country-specific requirements regarding drug serialization and other rapidly-changing regulations, while processing large volumes of data with intelligence. The SAP Advanced Track and Trace application for Pharmaceuticals allows you to comply with international and regional legislation. It provides a corporate serialization repository, serial numbers management, and reporting capabilities. Reduce compliance costs for current and future serialization requirements, including country-specific reporting. Increase efficiency in your supply chain by gaining greater visibility into material movements down to the sales-unit item level. Manage large quantities of serialization data and adapt to changes in legislation. Track and trace serial numbers of retail products in a corporate repository. Report serial numbers in accordance with country-specific regulations.

THINQ is a thought-leader in compliance for the Life Sciences sector. They provide compliance solutions to a wide range of pharmaceutical, biotechnology, and medical device companies. THINQ has a special expertise regarding validation and is leading the change in how validation is managed within Life Sciences companies. THINQ provides comprehensive compliance program management and development--powerful, market-proven solutions that are custom-tailored to our enterprise clients.

Samarind RMS is a smarter way for you to manage your medical product information. Samarind RMS allows you to only enter data once, and you can reuse it as often as necessary. An example of this is the 'INN' which can be used once and reused for all IMA submissions, renewals and variations. This concept is applicable to all key data within the system. It has been proven to improve data quality and streamline workflows. Our pragmatic approach to systems design and implementation means that our customers can manage their licenses smoothly and efficiently, safe in the knowledge that our single-place-of-truth™ approach for regulatory affairs professionals delivers a complete end-to-end system. An electronic document management system (EDMS), which includes version control, template creation, and the ability to link with external document management systems like Documentum™, SharePoint™.

SANeForce offers a comprehensive CRM and sales force automation solution, primarily tailored for the pharmaceutical, healthcare and life sciences industries. SANeForce is designed to increase the productivity of marketing and sales teams. It offers features such as real-time order tracking, expense tracking, stock control, and territory administration. The platform supports medical representative reporting, allowing field sales personnel log visits, capture doctor interaction, and manage appointment directly from their mobile device. SANeForce's data-driven insights, analytics, and customer engagement strategies help organizations track performance, streamline their processes, and optimize their customer engagement strategies. The solution also includes features for compliance, making it an ideal choice for highly-regulated sectors that require meticulous records and adherence to standards.

Dow Jones Risk & Compliance, a global provider, provides best-in class risk data, web based software applications, and scalable due-diligence services to help organizations manage risks and meet regulatory requirements in relation to financial crime, third party risk management, international trade, and sanctions. Dow Jones Risk & Compliance is built on the legacy of the world's trusted newsroom. It combines the expertise and knowledge of a multilingual team of researchers with the industry-leading data scientists, technologists and analysts to provide actionable compliance content. Our solutions were created in partnership with leading legal and political advisors, including former regulators, to help our clients maintain consistency among global business units and teams.

ComplianceWire, a cloud-based, Part 11 compliant learning management system (LMS), was developed by UL Compliance to Performance. ComplianceWire is a workforce training system for pharmaceutical, biologics and medical device companies. It facilitates the management and proficiency of learners, as well as compliance status. ComplianceWire's unique role-based approach to compliance qualification and performance management allows users to meet stringent regulatory requirements while seamlessly managing the most difficult training assignments.

It's more than just a place to store names and addresses. It creates awareness about who received your message and how. It can also be used to retrieve current commercial information at any moment. It is a feature-rich database that can be customized to fit your business' needs. It's simple to use and was designed with pharmaceutical sales organizations in mind. Add-ons and development proposals can be tailored to your company's specific needs. ActisCRM is always accessible and allows for quick interaction via desktop and mobile apps that can be used to suit any part of your business. This includes traditional face-toface reporting, key account management, medical sales liaison, and management at all levels.

The enterprise content gap can be bridged to achieve global harmonization and local autonomy. Veeva Vault, a cloud-based enterprise content management platform that includes a suite of applications designed for life sciences, is a true cloud enterprise solution. Companies have traditionally had to deploy separate applications to manage data and content applications. Veeva Vault is a content management platform that can manage both data and content. Companies can now eliminate site, country, and system silos and streamline all aspects of commercial, medical, clinical and regulatory quality and safety. All Vault applications are built from the same core platform. This allows companies to gain efficiency and compliance by allowing for a seamless flow of documents between regions and departments. The content is always available, current, and in context throughout the entire development and commercial lifecycle.

Affytrac is our secure EHS Software for the Life Science Industry. It is currently used by biotechnology, pharmaceutical, and medical device companies around the globe. You don't need to install any software. Our streamlined setup process makes it easy to have your EHS program automatically set up, tuned and available at all times. Affytrac is simple and intuitive, yet powerful and fully-featured. It does not have any extra complexity. Task Management allows you to define your organization's compliance and safety tasks. Affytrac tracks progress and notifies staff by assigning tasks to the appropriate personnel. Track and document Corrective Actions resulting from accidents, incidents, safety committees and regulatory inspections.

Enterprise Quality Management Software in cloud for life sciences. Technology plays a crucial role in ensuring that QA is aware of any issues as they arise in today's complex operational environment. You can gain insight into your quality management system's performance and the current state in your operation to be more proactive and reduce risk. Montrium's Enterprise Quality Management system (EQMS), was designed to help life science companies tackle the content management challenges they face head-on. Each module of the SharePoint QMS can be used separately or as part of a fully integrated quality management platform. These modules can be used on-premise or in a cloud environment. These modules are ideal for pharmaceutical companies, contract manufacturers, and medical device companies. Built to comply with GMP/GCP requirements.

Within3 is the leader in insight management for life science teams. Our insights management platform helps identify the right people, engage them and deliver answers that enable informed, agile decision-making. Our platform was created to address the life science insight gap. Companies often base decisions on outdated or incomplete data, which can lead to huge losses in time and money. Within3's insight management platform closes the gap in product development. It can be used at all stages of the product development process, including planning, recruiting, understanding, and analysis. Within3 is trusted by the world's leading pharmaceutical companies and medical device companies to identify key professionals, engage audiences in focused discussions, gain a 360-degree view on scientific and market signals.

You can speed up the time to market by organizing, executing and tracking all regulatory activities within a single RIM application. This allows you seamless access to all regulatory documents and full support for all eCTD submission requirements. Automation is integrated to streamline workflows and increase confidence in product registration data quality. You can speed up the time to market by organizing, executing, tracking, and planning all regulatory activities in a single RIM application. This allows you seamless access to all regulatory documents and full support for all eCTD submission requirements. Automation is integrated to streamline workflows and increase confidence in product registration data quality.

AmpleLogic Regulatory Tracker is built using the LOW CODE AND NEUTRAL CODE (LCNC PLATFORM) and consists of two modules: ANDA Tracker and DMF Tracker. This Pharmaceutical RIMS Software will help you improve data quality, increase operational efficiency, reduce mistakes, and streamline communications across departments.

IQVIA Smart, our new end-to-end regulatory information management software, streamlines regulatory processes. Your team can focus on delivering high-quality products to the market instead of labor-intensive maintenance. RIM Smart, the modern regulatory information management system, is designed to improve speed, collaboration, efficiency, visibility, and performance across your entire global portfolio. It also reduces costs. IQVIA RIM Smart is a secure cloud-based solution that allows for interconnected, comprehensive, and intelligent management of all regulatory processes. IQVIA safety platform integration will increase performance and improve flexibility. Automate manual processes and increase connectivity to improve efficiency, cost savings and coordination as well as cross-enterprise visibility and visibility.

RegDocs Connect provides the tools for your regulatory and operational teams to create compliant, submission-ready documents and records. This solution is built with the end user in view. It focuses on collaboration, automation, and quality. Automated workflows allow you to manage your records from draft to final. This allows your team to have complete control over your regulatory documents at any time. The mapping of document types to the EDM Reference Model and eCTD allows for organization and retrieval of documents that can be used in regulatory submissions. The powerful tools of PDF/A Publishing, document classification, unique document identifiers, and EDM reference model facilitate regulatory document management. This solution pulls together information from all levels of your organization into one easy-to-use solution. The ability to produce submission-ready and quality content has become more difficult due to electronic submissions to regulatory authorities and the complexity of drug development.

Software that allows you to track and organize Quality Risk Management information online. It uses web-based technology to trace Quality information to the specific risk it poses to the patient or drug product. Why Choose Us? CINCO is a risk-based software for quality management in the Life Sciences Industry. It allows transparent quality decisions by allowing for paperless traceability of all critical quality aspects of a drug or medical device. Why Risk Management? Quality Risk Management is a method that identifies and mitigates the risks associated with a drug or medical device manufacturing operation. Most regulatory agencies require it. The paper-based approach used by the Life Sciences Industry is ineffective in managing significant and valuable risk data. It is susceptible to errors, introduces too many friction to users, and does not add any value to the operations. Access to the most critical information about the product on-demand

The Life Sciences industry has been subject to nearly $15 billion in compliance-related settlements and fines over the past few years. It is therefore critical that companies adhere to best practices in pharmaceutical, biotech, and medical device manufacturing. A well-managed clinical trial can have a significant impact on the development time, budget, and scope of a drug or medical device. OpenText™, Clinical Trial Quality Management System, (ctQMS) allows companies to remain compliant, reduce the cost of records management, and establish best practices through collaboration during, and after, the clinical trial.

Our cutting-edge platform, the Medidata Clinical Cloud, transforms clinical trial experiences for patients, sponsors and CROs. The Medidata Clinical Cloud is the only unified technology platform that focuses exclusively on clinical research. It addresses every step of the research process, from start to finish. Our platform helps medical device and life science organizations reduce development costs, minimize risks, and bring treatments and devices to market quicker. The Medidata Clinical Cloud will allow you to access the power of any product you choose for your clinical trials program. Medidata is leading the digital transformation in clinical research. Our platform, powered by artificial intelligence, machine-learning, advanced analytics, and advanced research, brings together researchers, study managers and investigators to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials.

Platforce CRM, a cloud-based CRM that automates industry-specific business processes and improves customer engagement, is a closed-loop marketing and customer relationship management solution for pharmaceutical and life sciences companies. The system allows you to manage all aspects of marketing and sales activities, from the marketing cycle creation through territories assignment, databases creation, calls carrying, and KPI analysis.

Loftware Prisym 360 offers innovative content management features that incorporate industry best practices. It is specifically designed to meet the complex regulatory requirements for clinical supplies labeling. Many clinical labeling teams use English MLT/CLT variants for defining the content of booklets and labels for clinical trials. The number of countries in each study increases and each country has specific regulatory content, phrases, and language requirements. Therefore, the manual process of designing booklets and printing them takes longer and is more risky. Prisym 360's CLT/MLT solution prompts users to provide study information. Then, it automatically generates MLT, CLT, and booklet designs based on its knowledge about content and design requirements. This reduces the time it takes to create a clinical label or booklet, reduces errors and ensures compliance with regulatory requirements.

Aktana uses embedded artificial intelligence, which is refined by real-time human insights, to give life sciences sales and marketing professionals the information they need in order to improve customer experience. Aktana's AI-driven next best-action platform integrates seamlessly with every data source and player in your commercial tech stack. This transforms mountains of data into clear recommendations that are delivered into existing workflows. By embedding intelligence throughout the entire omnichannel ecosystem, Aktana makes every customer journey feel like a continuous conversation--seamless, well-timed and always relevant. Today, more than half the top-20 pharmaceutical companies worldwide use Aktana’s AI-enabled Contextual intelligence Engine to coordinate and optimize personalized omnichannel interaction at scale.

Pepper Flow's unique features were created to streamline the work of life science companies in marketing, legal, regulatory, and other areas. Marketers need tools that make it easy to work quickly and efficiently during promotional reviews and advertising. To support your organization's strategic goals, get your key campaigns and content to the market. Collaboration in real-time allows you to respond to feedback and make revisions. This will maximize productivity. Spend less time managing the review process, and more time focusing on your most important tasks. Pepper Flow, a cloud-based enterprise-grade software, enables life sciences companies to increase their competitive advantage, market their products efficiently, and maintain strict compliance. To deliver content to your key audiences, you need to be able to move quickly. Pepper Flow's intuitive interface makes it easy to complete work quickly and effectively.

BaseCase, Certara's leading value communication platform and market access platform, is available from Certara. Its suite of SaaS products allows pharmaceutical, medical device, or diagnostics companies to better engage with payers, healthcare professionals, as well as other key stakeholders. The interactive mobile apps allow them to create personalized value stories and use mobile apps to do so. BaseCase is unique in that it combines 'no code' content creation with integrated value communication on one platform. This has transformed the way life science companies think about product and how it's communicated. The life sciences industry's complete value communication platform. Integrated content creation and KAM enabledment allow for unparalleled flexibility and speed. You can create cutting-edge mobile content quickly and easily without programming. This will dramatically reduce your workload as well as your costs. Integrated content creation and KAM support on one platform will help you get to market faster.

Montrium is a knowledge-based business that uses its deep understanding of GxP technologies and processes to provide cost-effective solutions for life science organizations. Montrium Connect, the industry-leading platform for managing regulatory content, processes, and compliance in life sciences, has been designed to meet the needs of the new pharmaceutical business model. Users can collaborate and find the information they need faster and easier with intuitive navigation, enhanced user experience and dynamic content management.

Cloud-first ERP is specifically designed for life science organizations. Merit for Life Science, a cloud-first ERP, is specifically designed for biotech, pharmaceutical, and medical device manufacturers. It connects your entire organization with Dynamics 365 finance operations and finance. Mapping production requirements and resource qualifications. Monitoring vendor relationships in procurement to ensure manufacturing meets quality standards. Transparency and visibility for your life science organization to ensure safe and innovative products. We understand that every organization has its own unique needs. Get a complete overview of our services. We deliver a custom-tailored solution to meet the needs of pharma, biotech, medical device, and other companies. Using reliable, auditable accounting practices will improve your decision-making. Set financial reporting standards for acquired entities and prepare for acquisition.

Glemser offers IT solutions for regulated sectors with a focus in global life sciences and the ecosystem that enhances patient outcomes. ComplianceAuthor makes it easy for life science companies worldwide to manage product labeling, provide affordable IDMP, and reduce compliance risk. ComplianceAuthor for Global Labeling assists life science regulatory professionals to manage, scale, simplify, and streamline global product labels and compliance through artificial intelligence and structured content and natural language generation. Artificial intelligence and machine-learning are used to determine, index and derive the knowledge required to recommend the best course of action.

Our platform has decades of industry experience and is the only one specifically designed for life science companies. R&D Logic lets you and your team view plans and actuals from multiple perspectives so that you can always see how your business is performing. R&D Logic offers a personal service that will take care of your needs, from implementation through training to ongoing support and expert consulting. We manage the backend so that your data is secure and private so that you can concentrate on running your business. We take the time to get to know your needs and create the right combination products and logic for your business. R&D Logic's platform grows with you. As your needs change, you can add, remove, and modify features and business rules. No matter how small or large they are, we always put our customers first.

Accelerate scientific discovery, empower your R&D team and use harmonized data in cloud to accelerate your R&D. The Tetra R&D Data Cloud is the only cloud-native data platform for global pharmaceutical companies. It combines the power of the largest Life Sciences integrations network and deep domain knowledge to provide a future-proof solution to harness the power of your most important asset, R&D data. The cloud covers the entire life-cycle of your R&D data: from acquisition, harmonization, engineering, downstream analysis, and native support for state–of-the–art data science tools. Pre-built integrations allow for easy connection to instruments, informatics and analytics applications, ELN/LIMSs, CRO/CDMOs, and other vendors. Data acquisition, management, harmonization, integration/engineering and data science enablement in one single platform.

MonQual QMS includes pre-built, DMS, and LMS systems. It can also be integrated with other stand-alone systems. Integrate your LIMS (Laboratory Information Management System), MES(Manufacturing Execution System), SAP (Warehouse Management System), and other systems. This is true for both legacy and new applications. MonQual is everything your team wants. It combines quality, compliance management, business intelligence tools, and business productivity. You can take care of your documents and comply with regulatory standards by using the integrated DMS and LMS services. Quality deviations are part of the process, but we can prevent them from happening in the future. MonQual has processes that can detect deviations early, track them, run a root cause analysis, and then record and document them to prevent future ones.

Datatrak International, Inc. is a software-as-a-service provider of enterprise cloud-based technologies for the life sciences industry. Datatrak's unified eClinical solution and related services improve efficiency and cost effectiveness for the clinical trial industry. Datatrak developed its multi-component, comprehensive solution using a single platform. This concept was expanded to include services delivery through Datatrak's Clinical and Consulting Services groups. The Company offers a complete range of software products that can be used to speed up the reporting of clinical research data to sponsors and regulators. This is faster than using loosely integrated technologies. Our goal is to empower workgroups with role-based access, version-controlled file management and calendar events, tasks, and contacts. All built within our eClinical software applications, including EDC, CTMS and reporting.