Best Life Sciences Software in Mexico

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.

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.

A robust platform for automatic variant prioritization and clinical interpretation, as well as report generation, is essential to ensure efficient reporting of NGS-based clinical trials. Strand Omics, a cloud-based platform that is HIPAA-compliant and fast, drives our clinical diagnostics practice. It has been refined over 4 years with over 10,000 clinical reports and multiple peer reviewed publications. Strand Omics is a combination of bioinformatics algorithms and curated databases, visualization interfaces, and reporting capabilities. It offers specialized workflows that can be used for rare inherited disorders and somatic tumor profiling tests. The platform has over 10,000 variants curated to oncogenicity, 100 genes that are curated for druggability across multiple types of cancer, and 500 drugs that have been curated for evidence.

ESP is a unified, composable, and bimodal platform with a single data fabric that reduces the total cost of operations while enabling digital transformation for life sciences + healthcare. This FDA-compliant platform includes a number of best-in-class apps, including ELN, LIMS and Sample Management. ESP's REST API library and Python SDK enable flexibility and extensibility to meet customer-specific requirements. Each release is constantly updated with new applications. ESP ships with a wide range of pre-built connectors to lab Instruments, bio-process equipment, analytics, AI/ML, 3rd party software systems (such as ERP, CRM, EMR, etc.) logistics systems, bar-code printers, etc.

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.

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.

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.

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.

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

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

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

The biopharmaceutical market is complex today. There are growing demands for better specificity and safety, new treatment classes, and more complex mechanisms of disease. To keep up with this complexity, we need to have a better understanding of therapeutic behavior. Simulation and modeling provide unique opportunities to explore biological and physical processes down to the atomic levels. This can be used to guide physical experimentation and accelerate the discovery and development process. BIOVIA Discovery Studio brings together more than 30 years of peer reviewed research and world-class in-silico techniques like molecular mechanics and free energy calculations. It also allows for biotherapeutics developmentability and other related topics into one environment. It gives researchers a complete toolkit to explore the nuances in protein chemistry and to catalyze the discovery of small and big molecule therapeutics, from Target ID to Lead Optimizement.

Imagine a partner in commercial services that acts as an extension to your team. EVERSANA was created to accomplish this. We share a common focus on your business results. Ready-made infrastructure to protect capital. Integrated, actionable data provides metrics and accountability. Our integrated services can be tailored to meet any need, no matter how small or large. EVERSANA is the only provider that can work with life science innovators in any capacity. Our services are available at all stages of the product cycle, from pre-commercial to pending loss. Integrate our services to create a tailored solution to your challenges such as market access and distribution efficiency, patient adhesion, and many others. EVERSANA is a catalyst for the life sciences services sector. You don't have to rely on different vendors or service providers. We have created a platform for commercial services that functions like you do.

Genedata Biologics®, streamlines the discovery of biotherapeutics. This includes bispecifics and ADCs as well as TCRs, CARs-Ts, CARs-Ts, CARs, and AAVs. It integrates all discovery workflows, making it the most popular platform in the industry. This allows you to focus on innovation and is the most widely used. A first-in-class platform that digitalizes biotherapeutic discovery accelerates research. The platform simplifies complex R&D processes by allowing for the creation, tracking, testing, and evaluation of novel biotherapeutics drugs. It can work with any format: antibodies, bi- and multi-specifics as well as ADCs, novel scaffolds, therapeutic proteins, and engineered therapeutic cell line such CAR-T cells and TCRs. Genedata Biologics acts as a central data backbone that integrates all R&D processes. This includes library design, immunizations, selections, panning, molecular Biology, screening, protein engineering and expression, as well as candidate development and manufacturability assessment.

PatientIQ was founded in Chicago, Illinois. It serves providers, payers, and medical device & health sciences companies. The largest platform for healthcare professionals to connect and improve patient outcomes. Provide healthcare professionals with the industry's best technology to practice data-driven medicine. All stakeholders in the U.S. healthcare system are under increasing pressure. Objective measures of patient outcomes are crucial to assessing "value". Although measuring outcomes can be complex, time-consuming, expensive, and complicated due to technological barriers, they are the most valuable currency for value-based healthcare in the future. The next big market opportunity for digital health is a transparent way to measure, analyze, compare, and compare outcomes across stakeholders.

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.

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.

PerkinElmer Signals Translational is powered by visual analytics powered TIBCO Spotfire®. This provides all the tools necessary to manage, search, aggregate, and analyze large data sets in a consistent manner for translational research. Signals Translational is powered by the industry-leading visual analysis platform TIBCO Spitfire®. It enables precision medicine studies using the most advanced biomarker discovery technology and patient stratification. Signals Translational's Linear Mixed Effect App allows scientists to rank the effects of multiple variables on a particular phenotype. They can also correct for random variables. Independent of the origin of patients, the genes that have the greatest impact on the progression of cancer can be identified. LME models have the advantage of correctly handling outliers and missing values, making them an effective tool for identifying potential biomarkers.

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

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.

ChemOffice improves scientists' productivity and helps them do better research by allowing them to organize and explore chemical reactions and their properties. This allows them to turn data into actionable information and make more confident decisions. ChemDraw Excel adds chemical intelligence to Excel spreadsheets. Chemists can use Excel's sorting, organization and analysis tools to further manipulate and enrich sets and data as well as explore structure-activity relationships. Chem3D creates 3D models that allow chemists to view their compounds in three dimensions. This allows them to evaluate shape and properties to maximize specificity or activity. ChemFinder is a chemically-intelligent personal database system that scientists use to organize their compounds and to search for and correlate structures with properties.

The Suite is secure and scalable. It features an intuitive interface that allows scientists to configure workflows for any technique, modality, or data type. Signals VitroVivo 3.0, formerly Signal's Screening, transforms raw data into actionable findings. Signals Inventa 3.0, formerly Signals Lead Discovery is the next-generation analytics software that allows researchers to seamlessly publish results across disparate data sources. A cloud-based electronic notebook that is easy to use allows for experimental data capture, materials management, collaboration workflows, and more. Flexible visual and automated instrument data processing to improve data quality and reproducibility. Rich interactive analytics and unified data management for scientific research results. Integration with partner systems and processes as well as internal systems is possible.

Signals VitroVivo unites assay development, low throughput to ultra-high-throughput production assays, High Content Screening, and in vivo studies so users can search across all assay and screening data in a single platform. Signals VitroVivo can be used for assay development and is flexible enough to handle more complex essays. It is also flexible enough to support a wide range of techniques and is scalable to high data volumes. Scientists now have the ability to use a consistent, repeatable pattern in data acquisition and data processing. Easy structure-activity relationship analysis of small and large molecules. This tool was designed to meet specific requirements for handling samples, treatments, and studies.

Signals Inventa is a next-generation data management platform for scientific results analysis. It is powered by PerkinElmer’s Signals Data Factory technology, which allows you to quickly access and analyze all scientific data collected during the research and development process. Signals Inventa can help you determine which tests are most effective, what next to perform, what you should test, and much more. Signals Inventa makes data ready for exploration by staging, normalizing, and staging it. Signals Inventa expands scientific understanding with a range of scientific-analytical methods, including R-group decomposition, chemical clustering, matched molecular pair analysis, maximum chemical substructure, blast search of both internal and external databases, and sequence alignment.

StayinFront's CRM solutions have been helping pharmaceutical companies succeed since over 20 years. TouchRx is a configurable solution that can be tailored to the needs of pharmaceutical companies. It is supported by a responsive support team to help companies maximize sales, knowledge, and productivity. Field teams must follow specific processes when promoting products in the highly regulated pharmaceutical industry. These regulations are often misunderstood to mean that CRM partners who offer solutions for field teams will adopt a cookie-cutter approach. While compliance with regulations like product promotion and sampling is important, what you offer in addition to these core features could determine your level of success.