Best Life Sciences Software in Mexico

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.

Transform your way of managing bids and tenders. Move processes and data from disparate spreadsheets to one platform. XS Suite has you covered ensuring maximum ROI on every tender with hundreds of out-of-the-box functionalities. eXtensibility is a concept that allows for a wider range of options and functionalities. It connects all stakeholders in the tendering process to ensure everyone is aligned on the main objectives and goals. A one-stop solution that addresses all the needs of a tender office representative. Managerial business tool to monitor performance, including contract compliance and business development over many years. You can monitor your tender life cycle in real time and use advanced analytical tools for insights to gain an edge over your competitors. Quickly and easily generate reports that track the Company's business bid and tender activities.

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.

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.

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.

Infor PLM Process (Optiva®,) is a product view that provides a single view of all data and processes across an organization. It is specifically designed for life science, food, and beverage manufacturers. It allows manufacturers to easily comply with regulatory and labeling requirements. This includes meeting reporting requirements, complying under labeling laws, and supplying ingredient details. Project management capabilities allow the right people to have full visibility into project data, from concept to final sign-off. Reckitt Benckiser (RB), a multinational British consumer goods company, uses modern PLM capabilities with Infor(r] PLM for Process to increase global safety and compliance. It also gets one version of the truth about its products from development to manufacturing. Integration capabilities with ERP systems allows for better insight into costs.

eCADinfo, a 21 CFR Part 11 compliant, engineering data management system, was specifically designed for the life sciences industry. It is designed to reduce costs, improve efficiency, productivity, and comply with FDA-regulated environments. eCADinfo can store engineering data in a variety of formats, including engineering drawings, equipment/system specifications databases, web links with supplier sites, spreadsheets containing data about device parameters, manuals, and shop sketches. This system allows you organize the data in a structured hierarchy that provides meaningful information that best suits your business processes. The user interface is rich in graphics and provides easy system maintenance and control. Version control, collaboration, change management and standardization are some of the engineering data management features. The Excel spreadsheet environment is 21 CFR 11 compliant.

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.

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.

KonnectCo, Freyr's workforce management program, was specifically designed for the regulatory industry. It is structured to increase employee efficiency. It assists in managing and improving the reliability, productivity, and efficiency of customers' human resources needs including accomplishment and training management, programming and information gathering. KonnectCo provides insight into business metrics that allow you to compare workforce utilization with project and workload requirements for any given period. It allows you to analyze your daily work management and performance levels. It can also be used to analyze and plan for human resource management (HRM), such as attendance, performance management and compliance, payroll, leave planning, and forecasting.

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.

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.

Your supply chain is only as strong and as weak as its weakest link. If that link fails, it can cause business disruptions that can lead to catastrophic losses for your operations. SCAIR®, which identifies weak links, helps you strengthen your supply chain and turn bigger profits. All industries face huge challenges in 2020, but the Life Sciences sector is the most affected. This sector was hit with the double whammy: disruptions to supply chains and a huge increase in demand for medicine. SCAIR, an award-winning supply chain mapping tool, helps manufacturing companies visualize their global supply chains. Its unique flow-chart-driven structure makes it easy to map supply chains, quantify business interruptions losses, and stress test different supply-chain contingency scenarios. An intuitive graphical interface allows for instant visualization.

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.

Inovalon ONE®, Platform's industry-leading capabilities enable our clients and partners success by leveraging extensive industry connectivity and massive primary-source real data sets, sophisticated analytics and powerful cloud-based technology to improve the outcomes of healthcare.

TraceLink is the most prominent digital platform company in the life science supply chain. It brings together hundreds of thousands of healthcare and pharmaceutical organizations for the greater good for patients. TraceLink's digital solutions provide the visibility, precision, and agility necessary to enable all members of the pharmaceutical industry to thrive in a world that is constantly changing.

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.

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.

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.

Aetion Evidence Platform®, provides real-world evidence to life sciences companies, payers, as well as at-risk providers. We help you answer the most important questions in health care: What works best for whom and when? Better answers mean better decisions. Aetion is a trusted partner to most of the top 20 biopharma companies, leading payers, as well as the FDA. This helps inform the industry's most important decisions. Our transparent analyses help guide product development, commercialization, payment innovation, and the transition to modern health care. The Aetion Evidence Platform transforms the application of real-world data from descriptive analytics to causal conclusions. It delivers quick results, with answers in days or weeks. This is critical for improving financial and clinical outcomes. Transform your best information into useful insights that you can use immediately.

You can instantly master and link data in real time to resolve patient identity. Life sciences organizations can transform protected health information into universal, deidentified HealthVerity IDs. This allows them to accurately build and share the patient's journey across multiple partner datasets while also creating a single source for patient identity. To better understand the patient journey across departments, enable internal enterprise data sharing. External data exchange is possible with patient registries and health insurers, as well as other companion companies. The first step towards a data strategy that is based on data activation, data interoperability, and patient longitudinality is HealthVerity Census. It uses a state of the art PaaS de-identification system to activate both internal and external touch points, and data that is isolated in silos throughout the enterprise.

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.

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.

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.

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.