Alternatives to Veeva Vault

Interfacing's Digital Twin Organization software offers transparency and governance to improve quality, efficiency, and ensure regulatory compliance. A single platform allows you to map, analyze, and automate your processes, manage regulatory compliance, and assess risks. Interfacing's digital twin solution (Enterprise Process Center-EPC) is an enterprise management platform that allows companies to digitally transform their processes. It helps them streamline operations, improve productivity, and make things more efficient. Interfacing's digital platform - Rapid Application Development Tools (RAD) Tools, with its Low Code Development methodology, will optimize your technical resources and maximize transparency to allow for continuous improvement. Discover how our Low-Code Rapid Application Development module gives you all the tools needed to create and deploy custom, scalable, secure, mobile-ready applications in days vs. months!

QBench allows you to keep track of all your samples and where they are located in the workflow using a single system. QBench eliminates the need for spreadsheets, shared folders in the network, and paper-based tracking systems. You can view hundreds of PDF reports/COAs before publishing or emailing. You can generate barcodes and create labels that you can customize for your samples. Compatible with standard printers and scanners. QBench's billing module allows you to create and send invoices right from the system. You can see counts and latencies for different data types in QBench. This includes metrics like turnaround time, sample counts per test, sample delay, and many others. QBench makes it easy for you to gather the data your lab needs for the assays you perform.

Orange Logic is a powerful platform for digital asset management that helps ambitious content creators and growing businesses increase their control, creativity, and commercial advantage. Our user-friendly, infinitely scalable DAM solution streamlines workflows, automates processes, and removes roadblocks to remote collaboration. Orange Logic has created a highly intuitive interface that is designed to meet every departmental requirement, maximizing user adoption across the company and unlocking workflow efficiencies. OrangeDAM is trusted by Fortune 500 companies in the fields of Healthcare, Marketing, Manufacturing and Media & Entertainment.

Doxis Intelligent Content Automation (ICA) is the next generation of enterprise content management. Powered by AI, the platform connects and automates content to deliver a contextualized content experience and create a future-ready digital workplace.Doxis integrates with a wide range of business applications. The Doxis platform offers cutting-edge solutions for document management, invoice automation, contract management and human resources, in addition to solution suites for business-critical areas like purchase-to-pay. The strategy of the Doxis platform is to help organizations achieve a faster time-to-value, reduce IT bottlenecks and accelerate digital transformation. It does this by empowering business users, e.g. LOB leaders, department heads and project leaders, to quickly and easily customize and roll out content apps honed to their unique needs. These apps are available in the Doxis Fast Starter library, which provides a wide range of pre-configured and easily customizable workspaces for sales, purchasing, service, legal, etc. and for specific sectors like real estate and insurance. Leading market analysts recognize SER as a leading vendor of the enterprise content management market.

It can seem like a never-ending series of tradeoffs to bring breakthrough products to market within highly regulated industries. MasterControl's GxP software simplifies workflows, so you don't have to compromise quality for cost or innovation with regulation. Complete and connected meets flexible and fast. MasterControl Quality Excellence transforms quality data and processes to a competitive edge. Modern software is the first step in modernizing your manufacturing operations. MasterControl Manufacturing Excellence, from work orders to production records (EBR/eDHR), to logbooks and work instructions, is the easiest way to digitalize manufacturing.

A cloud LIMS that tracks samples, tests results, and manages inventory for life science research, industrial QC labs, and biotech/NGS. Includes regulatory support for CLIA and HIPAA, Part 11 and ISO 17025. The quality, security, traceability, and traceability for samples is crucial to a lab's success. Laboratory professionals can use the Lockbox LIMS system to manage their samples. They have full visibility of every step of the sample's journey from accession to long-term storage. LIMS analysis is more than just tracking results. Lockbox's multilayered sample storage and location management functionality lets you define your lab's storage structure using a variety location options: rooms and storage units, shelves and racks, boxes and boxes.

The AssurX platform is a powerful software platform for enterprise quality management (EQMS) and regulatory compliance to reliably communicate and coordinate information, documentation, and activities. AssurX allows regulated businesses to quickly identify and control quality issues and risk exposure to avoid quality or noncompliance problems while improving workflow. AssurX QMS software is uniquely configurable to fit any established or dynamic business requirements. The system creates an electronic workflow of tasks, alerts, escalations, and approvals that can be automated to the desired level, mapping precisely to real-world operations. No other system is easier to deploy, configure, and modify. AssurX solutions integrate seamlessly to create a connected quality system. Solutions include audit management, corrective actions, training management, compliant management, document management, change control, risk management, EHS incident management, and more.

Complex eClinical Solutions for EDC/ERT/eCOA significantly speeds up the start and completion of clinical trials (up to 5 days), reduces costs (up to 80% for monitoring), and increases capitalization and attractiveness (recognized by 89% customers). 96% of data science specialists say it increases the knowledge and advancements of Data Management and Data Science professionals. 94% of investigators love interfaces' usability. Strong internal competence in Data Management 365 is an important part of the Data Management 365 policy. This allows us to not only better understand the challenges faced by Data Managers and improve the MainEDC™, but also to transfer technology and best practices to our clients.

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.

Cloudbyz CTMS is a cloud-based trial management platform natively built on Salesforce Cloud. It is aimed at sponsors, clinical research organizations (CRO), and clinical sites for managing end-to-end clinical trial operations. Designed for clinical research, it expedites implementation and drives user adoption. Cloudbyz CTMS comes with an intuitive, straightforward design that allows for quick deployment. Boasting a rich set of features, Cloudbyz CTMS makes it easy for users to manage all aspects of clinical trials, including sites, enrolment, documents, events, milestones, site visit reports, finances, inventory, etc. The solution benefits are listed below- 1. Secure, reliable & scalable 2. Faster time to value 3. Monitor study progress & risks from planning to close-out 4. Seamless collaboration among sponsors, CROs & sites 5. Improved clinical team efficiency

OpenText Documentum is a tool that helps organizations overcome the information management challenges of today and create a framework for the future. Documentum helps you streamline content-dependent processes and improve enterprise governance. OpenText Documentum provides a wide range of capabilities to manage and extract value out of content of any type across the enterprise. The industry-leading enterprise content services allow organizations to control their critical information from a single source. This simplifies access to the most current, approved business content. Documentum's case management features combine content with process and automation to create complete case files. This streamlines business processes and ensures greater efficiency, consistency in quality, and faster cycle time. Users can quickly respond to regulatory inquiries and address information requests by keeping their content secure and protected.

DF mSafety AI, a cloud-based platform, uses AI/ML and automation for a great user interface and efficiency in Safety Case Management, Neutraceutical, Vaccines and Medical Devices. DF mSafety AI was built on Datafoundry’s Integrated Cloud Platform – DF Safety 4.0, which supports scalable, secure AI/ML-driven Safety Case and Signal Management. It also includes pre-built connectors for enterprise systems and adheres to industry standards and regulatory requirements.

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.

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.

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.

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.

End-to-end Product Data Management and Process Data Management. Skyland PIMS®, provides emerging and global drug sponsors and CMOs a collaborative space to manage critical development and manufacturing data. Our cloud-based, validated software is easy to deploy and has low total cost of ownership. Maintain data content, understanding, control, and transparency throughout the supply chain. Scale-ups, tech transfers, commercial releases are faster and more efficient. Access summary dashboards to view batch data, analyze and report on release status, data monitoring, and data monitoring. Manage process specifications and target control limits. Create an audit trail easily. Automated integration of Batch and Limits data allows for process analysis and control charts. Complete CPV/APR reporting requirements. For data integrity and transparency across global networks, maintain a consistent product and process data library. Streamline product data management throughout the product's lifecycle and supply chain.

Lyriko is an AI-driven platform that increases commercial efficiency and content effectiveness. It helps your business manage your customer base effectively by providing actionable insight for sales reps, and orchestrating content journeys. Lyriko helps Life Science Organizations achieve the Next Best Action paradigm for omnichannel engagement. Lyriko, a modular and scalable platform, is a complete AI solution that can cover all your commercial operations needs at a global scale.

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.

Model N is an end-to-end platform that empowers companies to maximize their revenue by transforming Sales, Marketing, Channels and Finance. Model N's revenue management solutions can help you maximize your revenue by turning tactical, siloed activities into strategic, end-to-end revenue processes using automation and intelligence. Revenue Cloud bridges the gap between back-office and front-office activities, providing a single system of record for all revenue execution. Customers can easily set up and quote complex products, quickly reach terms on complex contracts, have better channel data, which allows for visibility into channels and efficient management of incentive programs, avoiding overpayments. Model N Rebate Management allows you to better engage your channels and maximize revenue.

A data integration solution for modern science that is science-aware™. The data-driven future can't be built on the legacy architectures and broken data of the past. As research data volumes and types continue to grow exponentially, siloed data management and analytics become more and more unsustainable. For most organizations, however, this data is still spread across multiple systems. If the data has been brought into one place, it's usually done by a separate SDMS tool or business intelligence tool. This does not embrace the central role and highly integrated nature of truly scientific analysis. Jarvis is a science-aware™, data integration solution designed for modern science. It connects and harmonizes all of your collective scientific intelligence including instrument and application data so that you can maximize its value. Scientists can easily access this streamlined insight in a highly searchable living knowledge graph.

Digital asset management for the life sciences industry is integrated and allows global reuse, reducing costs on promotional materials. Marketing teams can easily publish or withdraw content from digital channels, ensuring only approved assets are used. Medical, legal, regulatory (MLR) software is industry-leading and can accelerate content approval and time to marketing. The built-in library of claims with reference links reduces administrative burden and risk when managing claims across channels, countries, and assets. Our industry cloud solutions offer data, software, and services, as well as an extensive ecosystem of partners, to support your most important functions, from R&D to commercial. Veeva helps businesses of all sizes to bring products to market more quickly and efficiently, and maintain compliance.

Inova facilitates life sciences partnership throughout all stages of the lifecycle. Finding the right partner or opportunity can be like searching for a needle in an abyss. To find the right information, you will need to sort through a lot of clues. Inova can help you find promising new opportunities quicker. The deal-making process can be lengthy, from managing due diligence to negotiating final terms. Inova streamlines key processes and saves time. Once a deal has been signed, it is time to make it profitable and successful. Inova can help you get started. Our digital partnering platform, which is market-leading, empowers more than 160 pharma, life science, and biotech companies to find, deal, and collaborate efficiently.

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.

IDBS Polar is the first BioPharma lifecycle management (BPLM) platform in the world. It eliminates repetitive manual tasks and allows you to execute your processes efficiently while curating data. This will allow you to accelerate the time to market, by tackling the most challenging challenges of process design, optimization scale-up and technology transfer. Interactive data analytics applications such as bioreactor comparision designed specifically for biopharmaceutical development scientists. IDBS Polar is an integrated platform that manages drug progress in contexts such as workflow, integration and insight. Workflows designed for the BioPharma lifecycle, with process-aware design, planning, and execution. Integrations that give meaning to your data. Rapid integration into your development environment, enabling automation, and curating a data backbone based on processes.

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.

OpenText ECM software connects content to digital businesses to increase productivity, simplify processes and improve governance, as well as control costs. Enterprise content management (ECM), software is essential for companies facing new operational challenges posed by COVID-19. Enterprise content management is responsible for managing the lifecycle, distribution, and use of information within an organization. This includes capture, archiving, disposition, and archive. The best ECM software enables organizations to integrate enterprise processes that produce information with one central content management platform. This improves information access and bridges isolated process silos. Governance is ensured wherever and whenever content is created.

Veeva Medical CRM allows you to build strategic relationships and connect with key stakeholders across all channels. Improve your understanding of key accounts and ensure alignment between teams. Engage across channels to create meaningful interactions. Planning, execution, and tracking of scientific engagements. Veeva CRM Approved Email and Veeva CRM Engage allow for multichannel integration. Coordinate planning and alignment of commercial counterparts. Control and compliance built-in, company-defined configuration, timeline view, activity between teams. You can gain a deeper understanding of your scientific interests and needs by gaining insights at the point of action. Communicate scientific content easily to create high-value interactions. Access compliant, version-controlled content. You can track and measure the performance of email and content.

ICyte is used by life science organizations of all sizes and complexity to facilitate pharma market access and commercialization. ICyte offers biotech and pharma companies world-class channel, patient and pricing data aggregation, contracts, pricing managed services and gross-to-net forecasting, accrual systems, expert launch and pricing transparency solutions, and pricing managed service contracts. ICyte helps pharmaceutical and biotech companies increase market access by quickly transforming channel, payer, complex transaction and patient data into actionable insights. ICyte also supports analytics-as-a-service, which allows common models and metrics to be deployed as a centralized service across applications, data, and analytics uses. The platform includes key performance indicators (KPIs), which are specific to Life Sciences companies. Also included are advanced analytics such as forecasting, scenario modeling, and a machine-learning-powered recommendation engine.

Enterprise content services platform helps you modernize, govern and manage business-critical data. Companies are not maximizing the potential of their content because more than 60% today's corporate information is unstructured. Organizations are looking to simplify their operations in the face of complex systems and an abundance of information. Rocket Mobius helps to dismantle silos of information, streamline processes, connect applications and simplify user access, while securing sensitive information across platforms. Modern technology tools and cloud solutions can help reduce costs, simplify workloads and reduce mainframe vendors. Reduce costs, vendors and complexity to improve productivity and legacy workflows. Organize, verify, and manage the lifecycles of information automatically, at scale, for low-cost regulatory compliance. Process improvement can make your business more efficient and competitive, and improve customer experiences.

PharmaWorx allows you to close the loop between customer feedback and marketing activities by providing real-time data capture. This also increases customer relationship. PharmaWorx allows Med Reps to make an informal or planned visit to a doctor's offices, and then instantly switch on their iPad/Android tablet to present product information to the doctor. They can also complete previously recorded tasks, take notes, or complete previous tasks. A doctor may be interested in a specific image, video, or brochure. The med rep can instantly switch on their iPad or Android tablet while they are still at the doctor's offices and present product information to them. They can also complete previously recorded tasks or capture notes for the current visit.

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.

ActivityBase is a proven industry software platform that manages screening data. It has a number of data analysis tools as well as built-in tools for registering objects and compounds. ActivityBase provides analysis for a variety of biochemical, cellular, and biophysical assay formats, including Ion Channel, FLIPR (Fluid Ionization Potential Resonance), Kinetic, SPR (Selective Pulse Response), and Mass Spectrometry. The system can be easily integrated into HCS imaging stores, such as Perkin Elmer Columbus (Thermo Fisher HCS Studio), Molecular Devices MDCStore, for easy data and image import. ActivityBase includes a built-in compound registration tool and plate management tools. ActivityBase allows you to easily track and manage results from years of tests in one system. The system can be configured according to your needs without the need to purchase new analysis packs. By improving your data analysis process, you can even tenfold your lab analysis.

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.

Kea is a complete CRM solution for Pharma companies, Hospitals and other organizations that meet APAC/Global requirements. Kea is a complete solution that allows sales and marketing teams achieve higher levels commercial excellence. Master Data Management, Closed loop marketing (CLM/e-detailing), Sales Force Administration and Events and Continuing Medical Education are all covered. Travel and Expenses automation, coaching, and many other processes are also covered. Kea tracks the response of patients to marketing activities in hospitals. Kea is a tool that benefits all users in the marketing and sales functions. It is easy to use and provides the required analytics. Users don't have to access multiple apps. Two pain points can be summarized in Kea. Users can view all KPIs for "effort" in a "one click" MIS dashboard. They can also track the "results". Kea can be modularized; some modules can be used in conjunction with Solutions such as Veeva CRM or IQVIA

Engage healthcare stakeholders in order to gain insights, advance research and share online knowledge. ExtendMed can help you maximize the frequency and quality of your interactions for a fraction of the cost. Let us help you increase your reach and impact. Health Expert Connect is a platform that provides scientific, marketing, educational, and training solutions to pharmaceutical companies, agencies, associations, and other organizations. - Hosting virtual advisory boards - Speaker bureau management: contracting, training, logistics, closeout, Sunshine reporting - Smartphone event engagement: sign-in, slides, polling, surveys, assessments, follow-up - Online product theatres and satellite symposiums

Providers and life sciences companies can use the platform to securely access cloud-based healthcare data and longitudinal EHR data. A collection of SaaS applications that can be used to manage the population, measure performance, and engage patients and providers. Allows healthcare systems to combine, link and combine data from hundreds different sources within their enterprise and clinically integrated network. It allows care and quality program developers to search and browse populations around diagnoses, treatment, outcomes and demographics. It quickly identifies target populations, allowing you to make better decisions regarding risk-stratified care management. A framework that allows you to correlate billions of clinical, financial and operational events into benchmarks and scorecards that can be used for comparison.

Titanium's comprehensive suite of applications is designed to keep your sample-management program compliant, efficient and streamlined in today's ever changing regulatory landscape. Our cloud-based SaaS platform offers unparalleled benefits that are tailored to comply with PDMA, 21 CFR Part 11, and other regulatory requirements. Titanium is a dynamic suite designed to address specific challenges in compliance while seamlessly interoperating. It provides an integrated and comprehensive solution that meets all your compliance requirements. Titanium is designed to grow with your company, ensuring each data point is only stored once and accessible across all applications. Integral audit trails provide transparency and accountability through seamless tracking and reporting. Titanium is a mature application that evolves regularly through upgrades. This keeps you at the forefront in compliance technology.

Our content services platform integrates seamlessly with your IT infrastructure and multiple databases to provide a highly scalable and agile enterprise content management system. It is designed for collaboration environments that allow multiple users to access a single interconnected database. GRM's CSP goes beyond a simple document management system. It's the best solution to create shareable files and optimize business workflows. GRM's VisualVault CMS allows a content management system that integrates data analytics, machine-learning, intelligent data capture, DMS software, and DMS software. It can manage documents, version tracking and high-tech security features. It also provides intuitive business process management (BPM), and Workflow Management Software. It was created to improve business processes.

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.

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.

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.

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.

Your sales reps should be able to see more doctors through Ammras organizer. A sales representative's effectiveness is measured by their ability to show the right materials at the right time. Ammras can help your representative do just that. It provides life science companies with the decision-support tool that analyzes real time market data, channel activity, and HCP (Healthcare professionals). This tool is designed to provide life sciences companies with insight, clarity, guidance, and the ability to deliver the right information at exactly the right moment. It uses data to extract only the most relevant and valuable information at the time of decision-making and present it to you and your field team. Our team focuses on simplicity and usability, so they can sell by making the most of their time to establish a strong relationship.

ysura conceives and develops innovative Sales and Marketing Solutions for the Pharmaceutical Industry and offers them as a Software-as-a-Service. Founded in 2012, ysura is based in Munich. It employs over 60 people from 17 countries. Ysura, an old Celtic word meaning Isar, is the name of the river that flows through Munich. It is a combination of ys (fast water) and ura(water). Ysura is short for fast water. Our products are fast and adaptable to the flow of information and tasks in the life sciences industry.

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.

Launch faster, smarter and with everyone in alignment. Meet the launch-ready software for agile execution. It's intuitive. It's built specifically for pharma. Your entire organization will want to use SaaS. Launches can be messy. SmartLaunch™, a new launch management system, brings everyone on the same page and ensures a better execution. Gain complete visibility over the entire launch program. No more waiting on status updates, spreadsheets, or slides. Say no to system sprawl. Align all stakeholders, across teams, countries and functions, at the same location. Unlock collaboration across functions and global/affiliated affiliates. Ensure a smooth and successful launch. Automating manual processes can save you time and money. Instead, focus on launching your new product. SmartLaunch™, guides you and your staff to the tasks that require your immediate attention. Prioritize your work using personal task lists, Gantt charts and flexible Kanban boards.

Legacy R&D software can be a drain on scientific potential. It slows down R&D progress and scatters data between silos. Benchling is the industry's most trusted life sciences R&D cloud. All the tools you need to accelerate, measure, and forecast R&D, from discovery through bioprocessing, all in one place. A suite of seven applications that are natively unified and can be used to accelerate R&D at all levels. Open integration, codeless configuration, and dashboards that are tailored to your needs. For continued success, deep life science R&D and consulting expertise are essential. Benchling is a unified R&D platform that allows you to spend less time searching for data and more time working together in order to advance your research. Scientists, managers, executives, and researchers can optimize R&D output by having complete visibility into the experimental context, program performance, resource utilization, and program performance.

Vault Training helps ensure job readiness and compliance through the creation and management of role-based training requirements. Vault Training unites document management and training. It allows life sciences companies to manage authoring approval, assignment, assignment and assessment of critical training materials from one place. You can easily manage your training content and deliver time-sensitive assignments using a single suite of quality applications. You can easily assign tasks based on your job function or role. You can track and complete training tasks, or monitor status via a role-based homepage. Training tasks can be triggered by quality events such as approval of content changes, CAPA plans or periodic reviews. Automate training assignments based upon job functions and roles. You can track, monitor, and demonstrate the competencies of your employees. You can also see the status of your training assignments with delivered dashboards or reports.

The L7 Enterprise Science Platform (L7|ESP®) is a comprehensive platform designed to contextualize data and remove business silos through process orchestration. This all-in-one solution supports the digitalization of data and scientific processes within life sciences organizations. It includes native applications like L7 LIMS, L7 Notebooks, L7 MES, and L7 Scheduling. L7|ESP seamlessly integrates with third-party applications, lab instruments, and devices to consolidate all data into a unified model. Featuring a low-code/no-code workflow designer and numerous pre-built connectors, it ensures rapid implementation and full automation. Utilizing a single data model, L7|ESP enhances advanced bioinformatics, AI, and ML to provide new scientific and operational insights. L7|ESP addresses the data and lab management needs and challenges within the life sciences sector, specifically targeting: ● Research and Diagnostics ● Pharma and CDMO ● Clinical Sample Management Explore the L7 Resource Center for on-demand recordings, case studies, datasheets, and more: l7informatics dot com/resource-center