Alternatives to Evidex

PvEdge, a cloud-ready software for pharmacovigilance, is designed to provide end-toend compliant safety solutions. It can be used with drugs, devices and vaccines. It provides a comprehensive database for safety that manages pharmacovigilance intake and case processing, submissions AI & Analytics, and safety signals, all on one platform. The system is compliant with existing and future regulations such as 21 CFR Part 11 ANNEX 11 GxP and GDPR. PvEdge uses advanced automation powered by AI algorithms and machine learning algorithms in order to improve the efficiency of drug safety database management. The platform's key features include automated literature scanning, ICSR submissions and smart triage. The platform includes a controlled document system for creating, publishing, and managing pharmacovigilance documentation, as well a risk-based enterprise management system that implements quality processes and records.

CoVigilAI, an AI-enabled solution for medical literature monitoring, uses advanced algorithms and data analysis to proactively detect adverse drug events and ensure patient safety and regulatory compliance. The platform allows for streamlined tracking of medical and scientific publications across global literature databases like Embase and PubMed, with customizable search string options to facilitate an effortless pharmacovigilance monitoring journey. The platform conducts periodic surveillance of scientific and medcial literature databases, as well as publications from local journals. This includes both global literature surveillance and localized literature. Advanced algorithms categorize Individual Case Safety Reports into valid, potentially invalid, and invalid cases. Automated key entity detection recognizes important entities such as patients, medications and adverse events.

Cloudbyz Safety & Pharmacovigilance Solution, a cloud-based solution, is designed to streamline drug safety and pharmacovigilance for pharmaceutical and life sciences companies. The solution automates the process of collecting data, processing it, analyzing it and reporting it in compliance with global regulations. Cloudbyz provides end-to-end management of the pharmacovigilance lifecycle, including adverse event processing, case management, regulatory reporting, signal detection, and risk management. With Cloudbyz, you can optimize your pharmacovigilance processes, accelerate case processing, and increase the accuracy of your safety data, while minimizing risk and ensuring compliance. The benefits of our solution are listed below- 1. Improved Efficiency with Automation 2. Increased data accuracy 3. Real-time visibility 4. Improved Collaboration 5. Enhanced regulatory compliance

DrugCard, an AI-enabled platform for data intelligence, is designed to streamline pharmacovigilance by automating the screening of local literature. The platform monitors over 1,000 local medical journals in 55+ countries and supports more than 100 languages, ensuring a continuous, regular and transparent monitoring. DrugCard automates routine tasks to allow Contract Research Organizations to manage more pharmacovigilance and improve screening results. Marketing Authorization Holders can conduct in-house literature reviews more effectively. And freelancers can save up to 70 percent of their time to perform other value-adding work. The platform is designed for new markets and to be cost-effective. It also complies with regulatory requirements.

Clinevo electronic trial master file (eTMF), is an electronic Trial Master File in electronic format (digital content). It can be used to organize and store documents, images and other digital content for clinical trials. Clinevo electronic Trial Master File eTMF has an inbuilt DIA reference model that meets regulatory guidelines.

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.

Clinevo Safety is a cloud-based, user-friendly, regulatory-compliant, end-to-end pharmacovigilance and drug safety system. This all-in one platform includes PV intake, case-processing, regulatory submissions through an AS2 gateway and analytics. It is built on a simplified tech stack and offers extensive configurations without requiring customizations. This results in a lower total cost of ownership and easy maintenance. The system alerts users when cases are approaching their due dates to ensure timely compliance. Advanced automation and AI features streamline the case processing effort, while easily configurable workflows speed up case management. Advanced analytics provide powerful and actionable insights. It is a web application that is easy to use and accessible anywhere, anytime and on any device using basic internet or intranet browsers such as Chrome and Firefox.

SafetyEasy by EXTEDO is a comprehensive multivigilance software that streamlines the processing of safety data and cases. It ensures compliance with a variety of drug safety regulations including E2B (R3) and HL7 eMDR and supports the production of essential regulatory documents such as PSUR PBRER and DSUR. The platform provides features such as workflow optimization via email notifications and online dashboards that allow users to track project progress and meet submission deadlines efficiently. SafetyEasy incorporates advanced modules such as CasEasy AI which uses Natural Language Processing to automate the case creation, and a Business Intelligence Module that provides a 360deg dynamic view of scientific data in order to enhance case analysis. SafetyEasy™ is a cloud-based solution that is easy to use, quick to implement and requires little training.

DF mSignal is a modular and scalable safety signal management system that enhances the efficiency of signal detection processes and risk management across pharmaceuticals and medical devices. It also includes cosmetics and nutraceuticals. The platform provides active and passive monitoring with real-time monitoring product-event combination, customizable clinical risk indicators, and an interactive interface with advanced analytics. It integrates seamlessly into MedDRA, WHO DD, clinicaltrial.gov and electronic data collection systems, providing a comprehensive safety solution for professionals. DF mSignal AI automates statistical scores to save time and ensure accuracy in signal detection. The system is designed to comply with all applicable regulations, including 21 CFR Part 11, data privacy and integrity controls, as well as GxPs. This ensures compliance and security.

The leading solution on the market for processing, analyzing and reporting adverse events originating from pre- and post-market drugs and biologics, vaccines and devices, as well as combination products. Improve your case management efficiency by implementing innovative capabilities such as workflow optimization, built-in automation and conditional touchless handling. Argus is a mature and reliable solution that provides proven compliance with drug and vaccine regulations and standards around the world. This includes E2B (R3), E2B (R2), eVAERS, eMDR, MIR, and IDMP. Oracle Analytics is a powerful, flexible AI-powered solution included in Argus Advanced Cloud. It allows users to discover new insights and make more informed decisions. The Medicinal Product Safety teams are under enormous pressure to manage an ever-increasing number of cases, new sources for signal detection data and changing regulations with limited budgets and resources.

Sentria is a platform powered by artificial intelligence that was designed for the management of adverse event cases and post-marketing surveillance. It is an intuitive, customizable and automated software solution that is industry-compliant. The platform ensures pharmacovigilance conformity with ICH international regulatory standards and ensures proper evaluation of adverse event following local regulations. Sentria streamlines the capture of reports using an intuitive interface, enhanced by pharmacovigilance automated alerts. It also reduces errors in report capture through intelligent alerts and facilitates processing of reports using international MedDRA and ATC/WHO codes. It improves analytical capabilities by using semantic artificial intelligence in pharmacovigilance. The platform has features like secure access controlled by credentials, auditable logs to ensure compliance, and an encrypted environment.

Tepsivo’s pharmacovigilance solutions are designed to streamline the drug safety process through automation and smart template, reducing administrative burdens as well as associated costs. The Tepsivo Platform, a cloud-based application, allows users to manage pharmacovigilance in a single location. Key features include a Quality Management System (QMS), Local Contact Person for Pharmacovigilance Oversight (LCPPV), streamlined safety reporting, follow-up tools and signal management tracking. Automated audit trails, compliance tracking and adverse event intake tools are also included. These integrated modules provide full transparency, 100% inspection readiness, high-quality, rapid speed, minimal cost, no administrative overhead and minimal cost.

Oracle Life Sciences Empirica, the leading solution on the market, is used to detect, analyze, and manage safety signals that originate in pre-and post-market drugs and biologics, vaccines and devices, as well as combination products. Oracle continuously researches, develops and advances the state of the art data-mining algorithm and statistical techniques that Empirica uses. Empirica's ability to detect signals with a longer lead-time allows it to provide risk insights 7-22 months earlier than label revision dates based on a time-indexed standard. Safety teams that are responsible for signal management have to face new challenges. They must find hidden signals, assess information from multiple large data sets, and provide better safety information even before clinical trials begin. Learn how new technologies and methodologies, such as artificial intelligent, can help to address these challenges. Read our ebook.

AccelSafety, a comprehensive pharmacovigilance solution developed by Techsol Life Sciences around the Oracle Argus Safety software, is designed to provide a unified platform for the collection, medical assessment and regulatory reporting of post-marketing and clinical safety surveillance data. The fully managed cloud-based solution helps emerging biopharma companies, devices manufacturers, and service provider to manage safety data and make informed business decisions aligned with global compliance requirements. The key benefits include Argus Safety implementation and migration with a 70% reduction in effort; secure migration of legacy data to the AccelSafety cloud; simplified lean cases processing through customized configurations, native automation, and comprehensive operational insights via advanced reporting, line listings, analytics packages, and 24/7 Argus Safety Service Desk Support for user requests, incident management, and change management.

PharmaPendium provides access to FDA/EMA drug approval documents including pharmacokinetics, pharmacodynamics, and safety profiles. It provides detailed information on drug interactions, adverse reactions, and clinical study results, allowing for informed decisions in drug development and regulatory filings. The platform's extensive database helps researchers and healthcare professionals evaluate drug efficacy, safety and effectiveness. This contributes to the advancement of pharmaceutical and patient care. Find out about previous regulatory submissions, and use precedents to predict agency requirements. You can easily switch from table view to interactive charts and graphs and visual aids for easy data interpretation. Using normalized data, you can find information by adverse events (MedDRA), drug indications, targets, and endpoints. The result pages bridge the gap between preclinical and clinical research.

Orbit is a platform that helps small, medium and large biopharmaceutical companies scale their safety operations to global markets. It offers innovative solutions to global pharmacovigilance and safety oversight, with the goal of increasing global quality, demonstrating compliance, improving productivity and efficiency, as well as providing meaningful oversight for traditionally complex and siloed process. The key features are risk management and minimization which tracks global risk plan commitments and supports the local implementation of additional risk minimization measures; safety data exchange management and pharmacovigilance agreement management allowing oversight across global partnership; signal and surveillance, which covers signal management from strategy to detection activities, signal assessments, and tracking.

LifeSphere Safety is the only next-generation SaaS Safety Platform in production that enables touchless case processing, scalable regulatory compliance, and standard global pharmacovigilance work flows. Drive transformational change with LifeSphere NavaX's industry-leading capabilities. These include the latest innovations in analytics, automation, and GenAI technology. Automate repetitive safety tasks with artificial intelligence and robust automation. With the most robust support for global and local regulations, including regular updates to the cloud, you can operate confidently in any market. Use powerful, easy to use tools for dashboards and reporting, operational benchmarking and intelligent signal analyses.

Ennov's Pharmacovigilance Suite provides a complete solution for collecting, assessing and reporting adverse human and veterinary events in a single database. The suite provides advanced data analysis and signal detection tools to ensure compliance with global regulatory requirements. The system includes features such as efficient case intake and data entry with optimized user interfaces, flexible case input form, and searchable vocabularies. The system supports paper and electronic report formats, including CIOMS and MedWatch 3500s standards (R2 or R3), as well as ICH E2B. It provides powerful analysis capabilities and comprehensive data queries for signal detection and management. The platform is 100% user-friendly and designed to comply 21 CFR Part 11 ensuring data security and integrity.

Clarivate's Drug Safety Triager, a next-generation pharmacovigilance system, is designed to help life sciences organizations meet regulatory requirements. This GxP validated, compliant and audit-ready software manages and streamlines literature review workflows, allowing pharmacovigilance specialists to focus on patient care by simplifying literature reviews. The platform is fully compliant and validated with global safety regulatory agencies like the FDA and EMA. Each implementation of Drug Safety Triager comes with a validation pack. The validation process, as well as the documentation that goes with it, is aligned with pharmaceutical industry regulations and health authority regulations. All literature references are subjected to a systematic review that captures all user actions and creates a permanent audit trail.

Veeva Vault is a modern system for managing individual safety reports. It supports the intake, processing and submission of adverse event reports for clinical and postmarketed products. Sponsors and CROs are able to process global and local adverse events for drugs and biologics as well as vaccines, devices and combination products. The integration of gateway connections and reporting guidelines streamlines the submission management and distribution of cases to health authorities. Central coding dictionary management automates the semi-annual updates to MedDRA, WHODrug and EDQM. Vault Safety integrates pharmacovigilance processes and systems on a single cloud-based platform to provide proactive patient safety. It uses real-time dashboards, reports, and collaboration to provide visibility for adverse events.

Flex Databases is an innovative, unified, and compliant electronic clinical platform that provides software solutions for clinical trials: pharmaceutical companies and CROs. Our system is composed of: - Clinical Trial Management System - Electronic Trial Master File - Project Management & Budgeting solution specifically designed for the clinical trials industry - Pharmacovigilance System - Learning Management System It was possible to create a flexible platform thanks to our unique experience and a qualified team of more than 100 professionals with a deep understanding the clinical trial process.

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.

Compier Literature Screening, an AI-driven platform, is designed to help pharmacovigilance practitioners efficiently screen abstracts, full-texts, and translated articles in order to identify patients, authors and safety-related data. The platform supports bulk uploading literature records from sources such as Embase, conference presentations and PDF journals. It also offers built-in integration to online biomedical databases like Medline. It performs automated duplication checks for every literature search, and uses validated AI models to automatically screen and annotate entities. Users can customize scalable literature screening workflows to meet specific requirements and global regulatory requirements. The system allows communication with third party vendors to obtain complete texts, and has built-in translation capability. It integrates with safety software, such as Oracle Argus Safety to transmit ICSR relevant articles.

Quanticate provides comprehensive pharmacovigilance, including the management and provision of pharmacovigilance databases. A pharmacovigilance database is the central repository of individual case safety reports for the company's medicines. These databases must be up-to date with the latest regulatory requirements, and validated in order to meet international standards and company needs. Quanticate stresses the importance of choosing the right database, taking into account factors such as implementation costs, maintenance costs, availability of hosting models (internal infrastructure or third-party hosting), prior experience, and compatibility with existing systems. They warn that, while many commercially-available databases claim compliance with ISO ICSR ICH E2B, true conformance requires careful setup and validation.

OpenSourcePV was founded by Lionel Van Holle, in 2019. The company's goal is to use free and open source technologies in order to raise standards in pharmacovigilance. It also aims to provide a cheaper alternative to expensive pharmacovigilance software. Pharma companies must monitor their products' safety to meet their regulatory obligations. As they begin to have multiple products and a strong pipeline, the amount data to be reviewed becomes too large to review manually. Currently, there are two options for companies to benefit from quantitative analysis: either they purchase expensive tools or they build their own. OpenSourcePV is a tool that helps them on their journey to quantitative signal detection. They can use pre-built modules or build something customized for their needs and data sources.

IQVIA Vigilance Platform, an integrated, comprehensive platform, is designed to simplify safety and pharmacovigilance while boosting speed and accuracy. Vigilance Platform is delivered in a secure SaaS environment using proprietary artificial intelligence, natural language processing, and machine learning algorithms. It delivers insights to improve compliance and product safety and add value to the product development process. The platform covers all aspects of pharmacovigilance, from capturing cases to case processing and submissions to all authorities. It also covers all types of cases. IQVIA Vigilance Platform is easy to use by affiliates, case-processing teams, and signal detection team due to its intuitive interface. A transformational approach improves compliance, so you can focus more on delivering safer and more effective drugs and medical devices.

TARA PV is an extensive web-based pharmacovigilance database that allows users to process, store, analyze, and report adverse events related with drugs, devices, or vaccines. TARA PV was developed by MedGenesis Ltd., an ISO 9001/ISO 27001 accredited UK software development company. It offers a user friendly interface that is intuitive and fully compliant to 21 CFR Part 11, GxP standards, ICH regulations, and global pharmacovigilance. TARA PV is a cloud-based software solution that does not require installation. It can be accessed via an internet browser. This allows for rapid implementation of integrated workflows and individual case assignments. The system comes with a full training package upon deployment. Support is available via an online ticketing system. Security is a top priority with hosting that includes multiple redundancies, triple-layer backups and other security features. TARA PV offers transparent pricing with no hidden fees.

NewTn SAFETY is a cloud-based pharmacovigilance platform that accelerates safety processes and simplifies compliance for pharmaceutical companies, startups and contract research organizations. The system includes a comprehensive set of features including cloud-based scalability, data reusability, real-time monitoring, alerts, and monitoring to detect adverse reactions quickly, and robust reporting functionality that facilitates the generation of DSUR reports and PBRER. The system's benefits are highlighted by tailored use cases, including establishing pharmaceutical safety databases in startups, providing cost effective safety systems for budget-conscious CROs, improving regulatory compliance for small- and medium-sized pharmaceutical firms, and delivering comprehensive data analysis and reporting. The platform's intuitive UI/UX, as well as its support for DSUR/PBRER reports, make it a custom solution.

TrominoCARE, a cloud-based Medical Information Call Center software, is designed to automate the daily operations of medical information call centers. It has a comprehensive database to support the entire lifecycle of MICC activities. This includes handling different call types, such as medical inquiries and product quality complaints. TrominoCARE is accessible via mobile phones and tablets as well as desktops. This ensures flexibility and responsiveness on all devices. The platform's key capabilities include process automation to manage all call types, automatic creation of Field Alert Reports, a configurable dictionary for client products, and customized workflows tailored to specific needs. The platform offers a mobile app that allows medical sales representatives and teams to capture and submit information offline. It also has integration capabilities for safety systems and MICC systems.

Biologit provides a comprehensive set of software and services to enhance safety surveillance in various industries. Their flagship product, the biologit MLM AI, is a global and local medical monitoring platform powered by AI. This scientific literature monitoring tool is easy to use, validated for compliance and fully web-enabled. It provides productivity gains for human and animal pharmacovigilance. The platform includes a configurable literature screening workflow that can deliver up to 70% productivity gains, powered by AI. It also has a flexible SaaS platform which is GxP compliant and CFR-11 compatible, as well as a database with major global and local sources of literature, with automatic article deduplication. Biologit also offers consulting services in pharmacovigilance and veterinary pharmacovigilance.

adWATCH – AE assists pharmaceutical companies to report adverse events that may occur during clinical trials. adWATCH – AE provides a quick and efficient way for a reporter at a clinic or hospital to generate and manage Adverse Event Reports (AERs), and report to regulatory agencies and government agencies. A negative or dangerous effect is one that a patient experiences due to the use of drugs or medical devices. Adverse event reporting involves the tracking of all medical complaint cases. This allows for the generation of MedWatch reports, CIOMS and additional reports for management. adWATCH – AE allows researchers, physician-investigators, Contract Research Organizations, clinical trial specialists, and other healthcare professionals to create and file AERs in FDA mandated MedWatch or CIOMS format.

SlimEDC, a cloud-based platform for EDC (Electronic Data Collection), is an EDC solution. The study editor makes it easy to launch retrospective and prospective studies, patient surveys (ePRO) and market research projects. SlimEDC can be purchased as software that is managed by the research sponsor, or as a service where the entire process, from the collection of data to its evaluation, is handled by a professional SlimEDC staff. SlimEDC has been adapted to the EU legislation and environment. The software generates all of the required reports for regulatory agencies. SlimEDC is ISO 9001 & 27001 compliant. Our team has received pharmacovigilance and BHBIA certifications. Independent authorities conduct strict GDPR audits on the legal and data security.

BIOiSIMTM, a revolutionary 'virtual drug engine', is the first-in-class tool that allows drug developers to narrow down the number drugs that have potential value in treating or curing specific diseases or illnesses. We offer a variety of translational-based solutions that can be customized for your clinical and pre-clinical programs. All of these solutions are based on our BIOiSIMTM platform, which is a proven and validated platform for small molecules, large molecule, and viruses. Our models are built using data from thousands upon thousands of compounds across seven species, which gives them a robustness that is rare in the industry. The platform is focused on human outcomes and has at its core a translatability tool that transforms insights across species. The BIOiSIMTM platform is available before preclinical animal trials begin, which allows for earlier insights and saves on expensive outsourced experimentation.

Kanteron Platform ingested digital pathology slides, medical images, and patient data from modalities and sequencers. It then provided a complete data toolkit for all hospital network teams. Precision Medicine at the point-of-care: Pharmacogenomics is used to prevent adverse medication events. It also incorporates data sources that have drug-gene interactions that were not previously available in easily accessible formats (e.g. Tables in a PDF document) and implementing the major Pharmacogenomic Databases (like PharmGKB or DGIdb, OpenTargets ...). This allows the user to refine their query to specific gene families, types, interactions, etc. Flexible AI allows you to choose the data set that is most appropriate for your use case and then apply it to your relevant medical images.

Scitara DLX™ provides a fast connectivity infrastructure for any instrument used in life science laboratories. It is fully compliant and auditable, and can be accessed from any cloud-based platform. Scitara™, a universal digital data network, connects all instruments, resources, apps, and software within the laboratory. The cloud-based platform, which is fully auditable, connects all data sources in the lab, allowing data to flow freely across multiple endpoints. Scientists can now spend their time on scientific research and not waste it trying to solve data problems. DLX corrects and curates flight data to support the creation of precise, structured data models that feed AI/ML systems. This supports a successful digital transformation strategy for the pharma and biopharma sectors. The ability to access scientific data allows for faster decision-making and drug discovery, which helps bring drugs to market quicker.

DNAnexus Apollo™, accelerates precision drug discovery through collaboration that draws critical insights from omics data. Precision drug discovery requires the collection and analysis of large volumes of clinical and omics data. These data sets are extremely rich, but many legacy and home-grown informatics tools cannot handle their complexity and size. Silos, insufficient collaboration tools, and complex regulatory and security requirements can all hinder precision medicine programs. DNAnexus Apollo™, which supports precision drug discovery programs, empowers scientists and clinicians to analyze and explore omics and clinical data in a single environment built on a robust and scalable cloud platform. Apollo allows them to share data, tools and analyses securely with peers and colleagues from all over the world, regardless of whether they are on another floor or another continent.

PubHive Navigator, an AI-powered platform, streamlines scientific literature workflows and safety workflows in life science companies of any size. It offers end-to-end solutions for literature review and curation, annotations, collaboration, searching reports, citing research, and managing it. The platform includes AI-powered smart workspaces that allow for centralized literature management. It also allows for collaborative research writing, team communication, reuse rights, and document delivery integrations. PubHive Navigator simplifies enterprise scientific literature and safety workflows. It is a flexible platform for teams working in drug safety, pharmacovigilance and clinical affairs.

The world's largest biomedical literature database will help you improve your biomedical research. You can find more biomedical evidence by searching the most up-to-date, relevant and comprehensive biomedical research. Use intuitive search forms to automate your queries and create systematic searches. Deep indexing manual curated to uncover drug-disease relationships. Comprehensive information is essential for biomedical research and drug development at an increasingly rapid pace. You can anticipate risk by assessing all that is known. To meet regulations, you track safety. You discover connections that can be used to drive innovation. Embase is a unique database of medical literature that goes beyond content. Emtree indexing full-text content and dedicated searches terms allows you to find all relevant and current results. This includes information that is not available in other databases. Scroll down to see why regulatory agencies recommend Embase for their best practice guidelines.

DF Literature Monitor, an advanced AI-powered system, automates the monitoring of large amounts of literature to optimize safety vigilance. It integrates with global and local literature sources to retrieve articles simultaneously, using semantic search. The platform offers automatic de-duplication and extraction of minimum safety data, as well as auto-population for safety case forms. These can be submitted in E2B, Excel/PDF, or Excel/PDF format to safety databases with just a click. It also offers automatic translation of abstracts and complete articles into English. DF Literature Monitor features configurable workflows that facilitate collaboration and quality assurance among pharmacovigilance groups. This solution allows teams to save up 60% or more in time and effort during the literature monitoring process, while maintaining quality and compliance.

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.

R&D and manufacturing labs must be able to change and reconfigure on the fly in order to accelerate new discoveries and bring products to market quickly. Data management shouldn't be a problem. Thermo Scientific™, Nautilus LIMS™, for Dynamic Discovery and R&D Environments was developed in partnership with customers. It is highly configurable and flexible. It increases workflow efficiency, throughput, data reliability, and simplifies administration, sample traceability, and regulatory compliance.

3decision®, a cloud-based repository of protein structures, is designed to manage structural data and perform advanced analytics. This allows small molecule and biologicals discovery teams the ability to accelerate structure-based drugs design. It centralizes, standardizes, and integrates experimental and in silico protein structures derived from public sources such as RCSB PDB, AlphaFoldDB as well as proprietary information, including formats like PDBx/mmCIF, and ModelCIF. This allows for easy access to X-Rays, NMRs, cryo-EMs, and modeled protein structures. It also fosters collaboration and enhances research efforts. 3decision®, beyond storage, enriches entries by adding metadata and sequence data, including annotations of antibodies, binding site details, and protein-ligand interaction. Advanced analytical tools can identify druggable site, assess off-target risk, and enable binding sites comparisons. They transform vast structural data into actionable information. Cloud-based platform allows for collaboration between research teams.

Cytel is the leading global provider of software for clinical trial design, biometric services and advanced analytics. They specialize in optimizing trials and helping pharmaceutical companies unlock the full potential of real-world and clinical data. Cytel was founded in 1987 by renowned statisticians Cyrus Mehta & Nitin Patel. The company has been at forefront of adaptive trial technology & biostatistical sciences. Our software solutions including the East Horizon platform enable precise trial design and simulation using adaptive and Bayesian methods to optimize protocols and speed up drug development. The East Horizon platform combines key components from Cytel's software portfolio into one unified solution, with R integration. This enhances trial design capabilities. Cytel also offers the Xact suite of software, a comprehensive toolkit that allows statistical analysis of small datasets and sparse or missing data.

PVSEARCH, a validated database management system, was developed by Owlpharma Consulting Lda. For pharmacovigilance specialists. It is a SaaS that supports medical literature screening by acting as a scientific repository linked to a robust and configurable search engine. Users can create queries by using predefined inputs, Boolean operators and automate searches in the database. The platform allows clients to add custom-created terms along with common terms in the database. This allows for a wide range of written variations, including nonstandard substances. PVSEARCH’s database includes a comprehensive collection relevant local publications such as journals and websites, newsletters and congress publications that cover human and veterinary healthcare in Portugal. Clients can choose specific publications to include in their periodic searches.

Eidogen-Sertanty’s Target Informatics platform (TIP), is the first global structural informatics system. It enables researchers to examine the druggable genome from an structural perspective. TIP increases the rapidly expanding body experimental protein structure information and transforms structure based drug discovery from an inefficient, data-scarce discipline to a high-throughput science with rich data. TIP is a tool that bridges the knowledge gap between bioinformatics (bioinformatics) and cheminformatics. It provides drug discovery researchers with a knowledge bank of information that is both unique and highly complementary to existing bio- and cheminformatics platform information. TIP's seamless integration between structural data management technology and unique target-to-lead analysis capabilities enhances every stage of the discovery pipeline.

CDD Vault allows you to intuitively organize chemical structures, biological study data, as well as collaborate with external or internal partners via a simple web interface. Start a free trial to see how easy it can be to manage drug discovery data. Tailored for You Affordable Scales with your project team Activity & Registration * Electronic Lab Notebook * Visualization * Inventory * APIs

Bibliovigilance, a search engine for pharmacovigilance publications, aims to streamline the monitoring of scientific and medical literature for safety information. It provides a comprehensive database that includes important national scientific publications from Europe and beyond. This database covers both human and veterinary product. The platform allows users to perform global search by running queries in PubMed, and accessing PRAC Safety recommendations on signals. This centralizes all literature searches. Users can save their searches, schedule automatic search, and choose only to search for new articles since their last search, saving time and reducing repetition. All searches are saved in a personal area that allows users to view and document their search histories at any time. The database is updated constantly, providing information about publications, the most recent update dates, and how many articles are indexed. This ensures transparency in the content.

BC platforms uses the latest science, unique technology capabilities and strategic partnerships to accomplish our mission of revolutionizing drug discovery, personalizing care, and transforming medicine. Modular, flexible platform that integrates healthcare data. Open analytics framework seamlessly combines the most innovative methods, technology developments and analytics in one platform. Superior security: ISO 27001 certified and GDPR and HIPAA compliant. A complete product portfolio allows modern healthcare systems to fully embrace personalized medicine. Scalable deployments allow for a robust start and large-scale healthcare operation. Our unique toolbox enables faster translation of research insights into clinical practice. Our unique toolbox helps reduce risk, increase your pipeline value, and advance enterprise data strategy. We remove the barriers to data access and enable rapid insight generation.

With unparalleled integrations of premium licensed content, open web and internal intelligence, you can aggregate, enrich and monitor important information sources at scale. InfoDesk’s information lab helps you identify the signal and eliminate noise. We have been building powerful tools for global analysis teams over the past 25 years. Our solution streamlines monitoring, analysis and reporting by leveraging our proven workflow, enhanced with enterprise-grade tools. This allows professionals to focus on high impact initiatives across regulatory and pharmacovigilance functions, as well as competitive, market and strategic intelligence. Centralize key data, streamline analysis and empower stakeholders with trustworthy intelligence powered by enterprise-grade AI. Our industry-leading deliverables engine puts trusted intelligence in the hands of your stakeholders. Dynamic dashboards will increase engagement.

Discngine Assay, a laboratory informatics tool, integrates all phases of plate-based tests into a coherent, compliant and efficient workflow. It is an essential tool for research labs that screen. It allows scientists to streamline their entire High Throughput screening workflow, from sample analysis and assay data storage to data warehousing to liquid handling equipment qualification. Discngine Assay's intuitive interface and robust API integrate seamlessly with Lab equipments, existing IT environments, and ensure efficient data capture and analysis. It is designed to accelerate the discovery of new molecules, while also addressing the needs of the pharmaceutical, biotech and CRO industries. This will enhance collaboration and drive innovation in life sciences research.