Alternatives to OpenText for Life Sciences

RegDesk is the most comprehensive AI-enabled RIMS platform for Medical Devices, Pharmaceuticals, and IVD companies. • Our proprietary Regulatory Intelligence for over 120+ countries is translated and accessible in a standard format. In addition, it provides alerts on evolving regulatory changes • Our AI-powered Application Builder allows RA teams to prepare and publish global applications in 1/10th of the time • Our Change Assessment capability helps RA teams understand the impact of the change(s) on an existing product(s) and the action required • Our Distributor Collaboration provides seamless workflow solutions to interact, communicate, and share documents with external business partners • Our Standards Management makes it easy for RA teams to search and manage not only international but also country-specific standards • Our Tracking & Reporting functionality allows teams to track regulatory projects across the globe, receive renewal notifications, and generate reports on KPIs within seconds For more information, visit our website.

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.

SAP Business ByDesign is an affordable, easy-to-use enterprise resource planning system (ERP) specifically designed for fast-growing small to mid-market businesses and subsidiaries of larger companies. From financials and inventory to customer relationship management and human resources, SAP Business ByDesign integrates all major aspects of your business for end-to-end visibility, added efficiency, and improved operational control. By serving as the nerve-center for your business, with all data flowing into a single, centralized system, SAP Business ByDesign enables real-time data access for faster, complete, more nimble decision-making. SAP Business ByDesign comes with workflows and best practices that help your business run operations more efficiently from Day 1. It also scales with your business, so you don’t have to change systems as you grow. Some of the key features of SAP Business ByDesign: Integrated system architecture that manages all your company dataSAP Business ByDesign Complete operational visibility and control End-to-end business process automation Precise real-time reporting and analytics Customization for business and industry-specific requirements Secure data access anytime, anywhere

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

OpenClinica is a leading provider of clinical data management software solutions. OpenClinica provides powerful tools to ensure that clinical trials are compliant and efficient. OpenClinica Enterprise, OpenClinica Participate and OpenClinica Randomize are the core products.

Qualio is a one-stop solution for quality and compliance management. It's ideal for growing companies in healthcare and life sciences. Qualio is reliable, affordable and easy to use. It helps companies build life-saving products faster and achieve 100% ISO, GxP and FDA compliance. Qualio makes it easy for companies to manage document control, training and NCRs, audits as well as suppliers, complaints, and other tasks in one platform.

BPAQuality365, a QMS software, can be used in your secure Microsoft 365 cloud. It leverages tools used daily by collaborators and does not require you to change your user habits. It is modern, compatible with all devices, adaptable to your specific needs, and powered through innovative M365 technologies. The app includes powerful compliance document management, audit, non-conformance, CAPA action, process and process maps, incident, change, risk, FMEA, SWOT, equipment, health, safety, environment modules compliant with ISO 9001, FDA Part 11 and medical regulations. The QMS app integrates with Teams discussions and users can ask the QMS while chatting in Teams and share QMS card with their colleagues. You can go further to achieve your Quality 4.0 goals by combining powerful AI features with best-in-class workflow automation and business intelligence. BPA's Microsoft Preferred status allows you to customize your QMS to meet your needs, share knowledge with your power users, and learn about M365 technologies.

Five of the most important regulatory agencies in the United States use MasterControl Quality Excellence solutions. A leading software-as-a-service (SaaS) provider, MasterControl helps companies get their life-improving products to market sooner. It does this by providing cloud-based solutions that manage an organizations documents, training and exams, corrective/preventive action, validation, and more. MasterControl offers solutions throughout the product's entire lifecycle.

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.

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.

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.

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.

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.

The industry's best AI-powered clinical analytics platform provides actionable insights that enable your teams to manage risk, improve performance across sites, studies, and vendors. Saama's state-of-the art clintech is designed to streamline workflows, automate tedious processes, and improve collaboration across clinical operations. Saama is trusted by sponsors and CROs for data aggregation, artificial intelligence solutions, and improved decision-making. This can help to reduce drug development costs and timeframes, as well as eliminate delays. Saama can help you get on the fast track for clinical trial process innovation. Your ClinOps and medical review team will find it much easier to access all of your clinical data in one place. Data managers are often undervalued. They can now focus on the data points that are important by eliminating manual work.

Cortellis™, a suite of life science intelligence software solutions, reveals hidden insights in data. This allows you to make better informed decisions throughout the R&D process. We have taken out the tedious work of finding, integrating and analysing data so that you can concentrate on the crucial decisions required to bring your products to market quicker. Cortellis provides unique data analysis that is rich in domain knowledge, industry insight, and therapeutic expertise. This allows you to unlock hidden insights that will allow you to make data-driven decisions that drive innovation. With the most comprehensive and deepest intelligence, you can get precise and actionable answers to specific questions throughout the R&D process. Cortellis is an indispensable part your daily work flow.

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.

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.

Deep 6 AI disrupts clinical trial enrollment by changing the way researchers identify eligible patient. DEEP 6 AI uses artificial intelligence and natural-language processing to mine structured and unstructed patient data. This allows DEEP 6 AI to find more patients that are better-matched for trials in a matter of minutes, rather than months. Deep 6 AI is used by some of the most prestigious health systems, pharmaceutical companies, and CROs around the globe. This makes the DEEP 6 platform an essential step in their clinical research workflow, greatly speeding up patients' access to clinical trial. Deep 6 AI locates more patients for clinical trials than it takes months. This allows people to receive life-saving treatments much faster. Deep 6 AI analyzes both structured data such as ICD-10 codes and unstructured clinical information, including doctor's notes and pathology reports. It also provides free-text access to important medical data that cannot be searched easily.

You can extract valuable insights from a variety of sources, all in one place. This will help you speed up the manual review process, increase productivity, and gain a deeper understanding of complex scientific content. Intelligent Literature Monitoring is a proactive tool that collects, evaluates, and documents post-market performance data in order to ensure compliance with the In Vitro Diagnostic Medical Devices Regulations, (IVDR), and Medical Devices Regulations, (MDR). Intelligent Literature Monitoring allows you to quickly and easily compare medical guidelines, and update visual decision-making tree. Our free, open-source content extraction framework can be used to extract text from a variety of data and documents. Language Intelligence Platform by Sorcero empowers life science and STEM companies with instant access to powerful insights that enhance expertise and decision-making.

Calyx understands that data is key to the success of any clinical development program. Your electronic data collection (EDC), system is crucial to your success. Calyx EDC is used in more than 2,600 clinical trials around the world. It streamlines data collection and reporting through one platform. Don't give your sensitive data to anyone. We can help you make your program a success with Calyx. Calyx EDC allows you to plan, design, and carry out studies of any complexity. Calyx EDC helps you keep your trial on track with features that reduce costs, improve site visibility and drive efficiency.

Unstructured health data can be unified and liberated with Interactive AI and NLP solutions that deliver health insights to Providers. Payers. Life Sciences. Interactive AI and NLP solution to unlock healthcare insights from unstructured clinical data. Provider. Accelerate data abstraction and clinical validation of clinical notes information. Reduce time and costs needed to identify care gaps, review care quality dashboards and create registry reports. Payer. To better manage high-risk and high-cost member cohorts, integrate and analyze claims data and clinical notes. Life Sciences. Use clinical trial databases and data taken from clinical notes to quickly match patients with clinical trials. Real world clinical data and evidence can be leveraged. Ember is a complete solution that combines NLP and predictive analytics. Streamline. Healthcare Analytics for Unstructured Data to Improve Quality and Efficiency.

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.

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.

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.

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.

ClinicalWave.ai, built on AWS' cloud platform, is an integrated AI platform designed for life sciences companies. It uses cutting-edge NLP to extract valuable insights and automates the redaction and extraction sensitive data from clinical documents. It is made up of: 1. ClinRedact AI - Our Redaction Product that automatically identifies and removes sensitive information from clinical documents. This product saves time and ensures data integrity. 2. ClinExtract AI - The AI Data Extraction Product that uses NLP and Machine Learning to extract relevant data from clinical documents. This product provides valuable insights and streamlines workflows. 3. ClinDICOM AI - Experience the power and features of our DICOM data extraction product. It offers targeted redaction, customizable redaction rules, intelligent context analysis, audit trail compliance and a user friendly interface.

Amazon Comprehend is a HIPAA-eligible, natural language processing (NLP), service that uses machine-learning to extract health data form medical text. No machine learning experience is necessary. Today, a lot of health data is found in free-form medical texts like doctor's notes, clinical trials reports, and patient records. Manually extracting data can be time-consuming and automated rule-based attempts at extracting data won't capture the whole story because they don't take context into consideration. The data is not usable for large-scale analytics that will help improve the healthcare and life sciences industry, patient outcomes, and increase efficiencies.

Our Smart Protocol system is designed to automate and add intelligence to clinical trials design with AI. Smart Protocol is revolutionizing how research teams design clinical trials. Humans can no longer physically digest all the information necessary to make a decision in today's digital age. A majority of companies have valuable data that isn't being used. Documents are stored in repositories without any line-of-sight. Companies in life science are making costly and difficult decisions based on incomplete information. We want to transform companies like yours' from a document-driven environment to one that is data-driven. We aim to reimagine how clinical trials are planned and researched by removing barriers between data and end users. We do this by mining huge amounts of trial-related documents both from customers and the public domain.

All researchers from different industries can use the same environment! ResearchManager is a platform that allows researchers to access all functions and information from one place. They can also share it with others. This platform is for researchers who are ready for the future. Future where patient and data access and sharing are central. We provide support for everyone involved in research in the life sciences sector. This is done through an online platform that includes the eClinical tools EDC and CTMS & ERMS. This allows researchers to share data and facilitates research at a higher level. We are also experts in the fields of data validation, enrichment, and collection.

eClinical Solutions assists life sciences organizations around world in their clinical development initiatives by providing expert data services and the elluminate®, Clinical Data Cloud -- the foundation for digital trials. elluminate, which is used by more than 100 biopharmaceutical companies worldwide, is a clinical data platform that was purpose-built to accelerate digitization efforts to manage the exponential increase in clinical data volume, variety and velocity. Gartner's 2022 Hype cycle for Life Science Clinical Development shows that life science companies are continuing to scale digital capabilities. The adoption of advanced analytics, hyperautomation, AI, and hyperautomation is becoming more mainstream. With elluminate's automated pipeline and scalable infrastructure, organizations can keep up with modern clinical trials and deliver business value across all clinical development functions.

Global life sciences industry trusts us to drive intelligent engagement. Intelligent HCP engagement across all channels in real-time can improve customer experience. Data science and embedded intelligence can be used to provide customers with the most relevant and effective messages. Field teams should have access to the most current information and insights in order to plan and execute calls. Compliant note capture can help you build deeper customer relationships. Pre-built and custom visualizations provide tailored insights at the point where execution takes place. Veeva CRM allows commercial organizations to use artificial intelligence in the way they choose. Veeva CRM Suggestions is an open model that allows you to implement the best actions with any data science provider.

Securely combine multiomic data from individuals with their medical histories to provide more personalized care. To support large-scale analysis, and collaborative research across entire populations, use purpose-built data storage. Use scalable workflows and integrated computing tools to accelerate research. Protect patient privacy with HIPAA eligibility, built-in data access, and loglogging. Amazon Omics is a tool that helps healthcare and life sciences organizations, as well as their software partners, store, query, analyze, and interpret genomic, transcriptomic and other omics data. The data can then be used to generate insights that will improve health and advance scientific discovery. To understand how omics variation is related to phenotypes in a population, store and analyze omics data from hundreds of thousands of patients. To reduce turnaround times and increase productivity, create reproducible and traceable clinical multiomics workflows. Multiomic analysis can be integrated into clinical trials to evaluate the efficacy of new drug candidates.

Cognidox is an online document-management system for high-tech, life sciences and medical device product development. Cognidox is available in the cloud and as an on-premise solution. It promotes product lifecycle management and knowledge sharing between developers and clients, partners, customers, and customers. Cognidox is secure and reliable. We offer plug-ins for many programs, such as Microsoft Office. We also offer an API that allows you to integrate almost any process with Cognidox. Cognidox's core function is a DMS. An add-on for Cognidox allows you to license and distribute documents to third parties via a fully sandboxed website. This allows you to publish specific documents while keeping your main storage secure. Another popular add-on is gBMS - Graphical Business Management System. Visio can be used to capture your business processes. A good BMS should give clear oversight of your entire operation.

TCS ADD platform speeds up speed-to-market for the pharmaceutical industry across all clinical R&D value chains and makes clinical trials more efficient and safer. TCS ADD facilitates digital ecosystems, simplifies data complexity, and provides patients faster access to effective drugs. The platform is powered with TCS Decision FabricTM cognitive artificial intelligence engine, smart analytics and IoT which provides superior business value for the pharmaceutical industry. The next-generation, end-to-end metadata-driven solution for managing industry and sponsor clinical standards. Data science-driven platform that uses AI & ML technologies to speed up study start-up, targeted interventions, and quicker decisions. This solution digitizes the entire clinical supply management process, while placing the patient at the center. This increases patient safety and overall efficacy.

Ripple, a web-based software solution that allows for the management and recruitment of research participants in clinical, translational, and social science studies is an active registry. Ripple was developed by researchers to transform the participant workflow. It is an end-to–end research participant management system that speeds up the entire research process.

IQVIA is trusted by thousands of organizations worldwide to accelerate drug development, improve product quality and safety and commercial effectiveness, get the right treatments for patients, improve healthcare delivery and access, and ultimately drive better outcomes. Connect data, technology and analytics to optimize clinical development. The result? The result? Faster decision making and lower risk, so you can deliver life-changing treatments faster. IQVIA offers specialized capabilities to customers in the healthcare industry, thanks to its foundation in data, advanced analytics and expert insights. Watch the latest from IQVIA data scientists and doctors, as well as other subject matter experts, on the topics that are important to you. You can find everything you need, from industry trends to how our capabilities are being applied to help, here.

Axtria SalesIQTM is the most popular sales planning and operations software for the global life science industry. It enables motivated sales teams to achieve greater commercial success. Axtria SalesIQTM empowers sales reps to make smart decisions and reach the right customers at a time that suits their needs. Simulating and what-if analysis allows you to seamlessly convert brand strategy into sales plans. You can launch any drug or medical device in any therapeutic area quickly and with total flexibility. Transform from product-centric to customer centric omnichannel interactions. Connect the dots between providers and territories, channels, incentives, and incentives. You can improve decision-making by leveraging trusted data from ingestion to insights.

LexisNexis®, MarketView™, provides medical claims-based information to healthcare payers and providers, life science companies, and health IT organizations throughout the United States. MarketView provides actionable insights that help businesses remain competitive. It allows them to see valuable insights and visualize ways to transform their business. MarketView is available to all life sciences companies, health plans, health systems, and vendors. It can transform key business work streams such as marketing, sales and strategic planning, physician outreach, physician relations, network optimization, market research, pricing, contracting and recruitment. To remain competitive, your business needs the most actionable insight. It can be difficult to pinpoint the right areas of focus if the picture isn't clear. MarketView provides insights into areas such as physician alignment strategies, referral patterns, physician referral patterns, quality of clinically integrated network, patient volumes, and more.

DXC RIM platform manages regulatory content, data and workflows in one central place. This helps teams accelerate innovation and reduces time to market. A unified platform is required to manage regulatory data and workflows due to the sensitive nature of regulatory affairs content (RA). All relevant data must be easily accessible to all teams. They also need an intuitive, customizable user interface that is simple to use. While configurable reporting and collaborative tools are essential for success, legacy technology can frustrate teams or slow down processes. Compliance is difficult. It is difficult to collect data and document processes. Life sciences organizations that use disparate technologies and have fragmented legacy systems can create problems. They may need to resort to spreadsheets in some cases to manage key operational processes. A centralized enterprise-grade solution is required to bring products to market and manage RA.

Axtria DataMAx™, the next-generation global cloud-based commercial Life Sciences Data Management product, enables accelerated business insights from trusted data. Axtria DataMAx™ facilitates rapid integration of all major structured as well as unstructured data sources in life sciences. It is secure, accurate, and compliant with the industry. To ensure that data is safe and reliable, business management rules and data quality are applied. Users can create data marts for downstream consumption and reporting by models, analytics systems, or individual data stewards.

Azenta Life Sciences provides scalable, flexible, and powerful informatics sample processing systems that allow lab systems to efficiently deploy across all locations and use built-in project management functionality. We offer unrivaled sample exploration, management, and delivery solutions to accelerate discovery, development and delivery. Azenta Life Sciences offers cloud-based informationatics solutions for sample processing. These solutions automate laboratory workflows, and reduce staff workloads through standard processes. Modules can be used to manage patients, families, clinical trials, informed consent, storage and diagnostics, as well as sample processing. Interfaces with external data sources are available and flexible options for integrating 3rd-party systems and instruments.

Your business will have easy access to unified data from multiple sources without the need for any programming. Lore IO's AI, prebuilt ecosystem of connectors and API allow for fast onboarding from any source. The user-friendly UI is flexible enough to adapt to changing business requirements. Unified data plays an important role in the development and launch of your product. Why rely on prebuilt, rigid, and expensive solutions that don't scale with your needs. Why not use custom-built solutions that are complicated and require significant resources to scale? The Lore IO Life Sciences Cloud Analytics solution is simple to use and allows business teams to access data at every stage of the process. Our pre-packaged solution integrates easily with your data sources* and provides insights in weeks, instead of months.

ZenQMS improves the quality compliance profiles life sciences companies through a cloud-based platform. It is purpose-built to facilitate document collaboration, control, training, issues management, audits, and change management. ZenQMS is a team of technology and quality leaders who share the common goal of making quality management a business imperative.

Revolutionize your Life Sciences processes. You can dramatically improve the quality, control, and efficiency of your products and processes. Our fully compliant platform is pre-validated according GAMP5. This ensures inspection readiness at all time. You have complete control over all documents and processes. You can also customize workflows and automate when possible. You can enjoy uninterrupted workflows and full traceability with seamlessly connected and integrated modules. Our dedicated team is available to answer any questions you may have. Only the best Scilife experience is possible! Our Scilife platform automates, automates and organizes all processes in your industry space, no matter if you're in Medical Devices or Pharma & Biotech or ATMP. Click below to see which Scilife modules are available for your industry's unique lifecycle stages.

In today's pharmaceutical manufacturing environment, it can be difficult to maintain consistent product quality and quality processes. To meet regulatory requirements, industries like the Pharmaceutical, Biotech and Life Sciences must maintain Good Manufacturing Practices (GMP). You must not only meet GMP requirements, but you must also be capable of proving it.

VIPER automates screening from remote patient identification (at point of diagnosis) through to qualified enrollment. VIPER uses artificial intelligence to match patients to precision trials within a narrow window of opportunity. This is done through the ingestion of lab-agnostic genomic and pathology data. It is tailored to the patient and the researcher. VIPER searches the personalized matching engine to locate the best clinical trials available for a patient's specific diagnosis--at that time. VIPER integrates workflow to send real-time notifications to the entire care team about a patient's eligibility in available clinical trials. This is done within a very limited enrollment window. VIPER provides interactive dashboards that allow you to access real-time data mining capabilities to aggregate patient data from both study and site levels to help you reach your study KPIs.

BatchMaster Manufacturing ERP Solutions can be used by formula-based process manufacturers in the Food, Chemical, Nutraceutical, and Life Sciences industries. Our software supports batch production, formulation, packaging management, batch production, quality and recall, lot traceability & rappel, industry-specific compliance, planning, scheduling, mobile warehousing, and other process manufacturing functions. Manufacturers can use their existing financial systems to run our process manufacturing application, including QuickBooks, Sage 100&300 and Microsoft Dynamics GP. We offer an ERP solution for manufacturers looking to replace or upgrade existing business systems. It supports specific manufacturing, financials and sales as well as supply chain, purchasing and customer service. Our applications are available on-premise (purchased), and in the cloud (monthly subscription programs).

OKRA.ai is changing the face of Life Sciences by utilizing intelligent brains. OKRA.ai transforms the pharmaceutical industry by providing services in the areas of medical, commercial, market access, and marketing. Learn how to access your AI brain and how it can deliver cost-effective solutions, resource-saving resources, and targeted patient outcomes for your organization, today. OKRA's MarketSphere is built with the best-in-class AI technology. It can turn insights into intelligence and guide your next steps. You can see the future up to 12 months in advance. Launch products, reinvest in or relocate resources to maximize your return. No matter what brand. No matter where you live. MedCompass allows medical leads to see the unmet needs of their community (KOLs, HCPs) across multiple markets and TAs. This tool allows you to see how topics change over time from a static perspective.

Inception CRM is an innovative sales and customer management solution for Life Science sales teams, supporting medical and pharmacy representives remotely and in the field. Delivered SaaS via native applications for iOS, iPadOS, Android and Windows, Inception CRM enables holistic customer relationships through a robust approach to customer data management and segmentation, with targeting based on real sales potential and priorities. Inception CRM supports complete time, activity and cycle plan management, and enables management of pharmacy orders, samples, and expenses. Built-in closed loop marketing, media sharing, and remote detailing features enhance the effectiveness of face-to-face and remote calls. Intuitive KPI dashboards and reports keep users and stakeholders aligned and maintain transparency across the sales organization. Inception CRM offers many prebuilt templates and workflows, ideal for clients of various sizes and orientation, and can be easily extended to support custom workflows and business processes on demand.

Ofni Clinical is a clinical database management tool that creates and quickly implements secure, regulatory-compliant clinical trial databases. Ofni Clinical offers comprehensive search and report capabilities, strong data validation and edit-check options, flexible customization tools, and is easy to implement quickly and economically. The databases can be used to collect data from existing Case Report Forms as well as electronic data capture systems that are paperless. Most Ofni Clinical projects take less than a month from project initiation to validation. Contact us today to learn more about Ofni Clinical and how it can be used for clinical trials. It matches your existing Case Report Forms, reducing training and implementation expenses while adding electronic data capture & review capabilities. Features include extensive edit checks and data validation to detect and correct data entry errors and support data analysis.