Alternatives to TruLab

eLabJournal: The comprehensive Electronic Lab Notebook (ELN) solution to optimise your life sciences research. eLabJournal offers a seamless solution for collecting, managing, and analysing research and laboratory data. Our open ecosystem software includes modules such as Electronic Lab Notebook, Sample Tracking, Inventory Management, and Protocol Management, along with a plethora of add-ons and integrations to suit your lab's unique needs. Enhance your productivity with eLabNext by simplifying documentation, organisation, search, and archival of data, samples, and protocols. Access your data securely through cloud-hosted ISO-certified data centres. Whether you're a startup, mid-size pharma, biotech company, or academic research group, eLabNext is designed to meet your industry R&D needs. As a brand of Bio-ITech BV, part of the Eppendorf Group, eLabNext brings reliability and expertise to your lab management solutions.

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.

Each specimen should be assigned a unique identification number and clinical data collected. You can catalog specimens to investigators, protocols, departments, investigators and institutions. Divide the samples into new specimens, each with a unique ID and associated data. Track specimens from collection through freezing/thawing, and eventual destruction. HIPAA compliant, with the ability to de-identify information. Manage multiple biospecimen repositories. Collect specimens at specific time points in the protocol calendar or via a single event. Track consents and other documents. To replicate physical storage, design freezer/storage container configurations. Multiple configurable reports are available for inventory, QA and consents, manifest creation/tracking and invoice creation/tracking. You can easily query the specimen repository for a specific sample type.

LIMSey is a cloud based software designed specifically for engineering, mechanical, and other labs which test physical products. Automate resource scheduling, track jobs, manage changing priorities, generate test reports, support regulatory audits and accreditation, manage equipment, calibrations, training records, and more. All features, updates, and support are always included with no additional modules to buy.

Mosaic is the most trusted sample management software for life science laboratories. Mosaic is trusted by a global customer base, from small biotech companies to large pharma companies. It tracks and manages every stage of the sample lifecycle. Keep a digital representation of all your samples and operational data, current and past. During every step of sample preparation, locations, amounts, and concentrations will be accurately recorded and audited according to 21 CFR Part 11 standards. Extensive, proven integrations with instruments or informatics platforms to support end-to-end research workflows. Validated requests are processed and automated fulfillment is performed. This ensures that there are no errors in delivery. From one scientist managing a small collection, to thousands of users managing hundreds of millions of samples, the operations can be automated. One system that can manage a variety of sample types including cell lines, compound libraries, proteins, nucleic acid, and many more.

In-system protocol and its training program. Equipted with fingerprint attendance. Cronos offers highly customizable if/workflows that can be used to conduct derma/ patch/ other early phase BA-BE/ phase studies. You can capture, cleanse, and manage your data from paper-based or EDC based trials. Data extraction in desired datasets is possible using standards such as CDISC (SDTM) EDC tool that allows for real-time activities. Its Bedside Data Collection capabilities allow for faster and paperless assessments. It also includes a sample inventory and tracking facility. Compliance-ready data repository.The facility of data e-printing from almost all BA instruments/software and online review of data in defined workflow with e-stamping and e-signature.Project-wise view, export & archival of data. High-quality statistical reports (tables and listings) can be generated in fixed/desired formats.

LIMS by ABI Health make it easier to grow your lab business. It takes only a few hours for collection and processing centers to be open. All centers can be managed from one platform. You can grow your business, process more samples and get real-time insights and reports. This is a great opportunity to scale up your business quickly! Batch Processing Samples. A batch of samples can be processed using LIMS' unique batch-tracking tool. This assigns a single code to each batch. The Workflow Manager allows technicians to track the sample handling and assign a barcode to it. Reduce standby time and eliminate confusion about where the sample is. Automation. Automation to save even more! Automation can automate repetitive and time-consuming tasks, increasing efficiency. All equipment and devices can be integrated on a single secure platform. This eliminates the need for manual data transfer.

CryoTrackIMS software is a complete package that can be used for molecular biology and cell banks. It can also be used to create clinical samples, biobanking, biochemistry and immunology. It can also be used for high-throughput screening, QA and IVF labs. You can create any type of box, plate, or pie configuration. Simply select rows and columns, or a Pie configuration. Your box will be created in seconds and you can start entering data. Basic research and biotech businesses require an inventory of valuable biological specimens and samples. It is difficult and frustrating to keep track of large quantities and types of biological samples (DNA,RNA, clones and proteins, peptides and probes. Antibodies, enzymes and enzymes. Samples can also be used for biotech business. CryoTrack provides a complete solution to individual labs at universities, clinics and biotech companies.

Novatek's Clinical Assay Management software provides a consistent approach for the collection, management, and integrity of clinical research data. Novatek's Clinical Assay Management software tracks all sample data and manages them throughout the entire analytical process. It also ensures that there is a single verifiable version of all clinical and analytic data sets. Novatek's Clinical Assay Management Software helps organizations manage their studies based upon a specific product. This application will also give the structure required to ensure that all steps are completed in a timely fashion.

AI advances will eliminate the need for trial and error in medical practice. Our digital twins allow for confident and rapid clinical trials. We work in neurology, immunology and metabolic disease. TwinRCTs achieve full enrollment faster because they need fewer patients in order to achieve the same power of traditional trial designs. Enrollment time in late-stage trials can be shortened. TwinRCTs increase the power of early-stage studies without adding additional patients, allowing them to observe treatment effects. Early-stage studies can be used to make confident decisions and attract participants. TwinRCTs increase the chances of participants receiving experimental treatments because they use smaller controls groups. Position clinical trials using digital twins to achieve regulatory success. Unlearn engineers the future of medicine using artificial intelligence. We create and deploy new types generative models based on patient-level data.

A platform that integrates EDC, eConsent and ePRO for efficient clinical trials. Replior is a company that provides software for clinical trials. Trial Online is a suite of software that allows investigators, participants, and wearables to collect and manage data in an efficient and easy way. Trial Online supports decentralized clinical trial (DCT) by allowing trials to operate with remote visits, site visits, or as a hybrid. Our journey began 20 years ago when we were asked to create an online CRF service by one of the largest pharma companies in the world. Back then, we were an IT operations provider for pharma. This was the beginning of software that allows for data collection in clinical trials. Today, we offer a complete suite of data collection software services. Our IT operation is handled by our certified sister company Complior.

AcceleTrial™, takes the guesswork out identifying and activating clinical trial sites. Our Study Start-up Management System is based on objective data, not self-identification. AcceleTrial™, a global database of thousands of sites, is indexed and ranked based on: Objective Site-specific Therapeutic Expertise and Objective Site-specific Clinical Test Experience. Objectively match the right sites with objective data on expertise, patient data, and experience to your clinical trials. AcceleTrial™, an automated "push-and-pull" structure, allows you to quickly launch the right sites and begin enrolling patients. It is available in multiple languages. Collect required documents accurately using pre-filled templates. Track activities in real time. You can immediately start using the system - a cloud-based solution that requires minimal IT setup or training. Integrate AcceleTrial™, CTMS, or other clinical trial system.

Accelerating the development and delivery of life-saving medicines, and enabling cancer patients to have access to the best quality of cancer research and care. Our software revolutionizes patient access to innovative drugs & clinical trials. FICS is a software that allows the collection of regulatory standards data during patient care. FICS combines traditionally separate and noncommunicating applications to create a novel end-to-end platform. This allows clinical trials to be performed faster, easier and with greater quality.

BioShare is a platform that allows researchers to search for available collections and to submit requests for specimens or data. BioShare provides a central location for researchers to search available collections and submit requests for specimens and data. It also allows them to track the approval and request process. BSI Systems supports data sharing as a way to increase the effectiveness and value of research among laboratories. BioShare is a web-based platform that allows researchers to share biospecimens or datasets with other members of the research community. BioShare is a central place for researchers to search, submit request and track all correspondence. It provides easy lab sample tracking via a user-friendly interface. It's now easier than ever to track specimens and data requests. BioShare's comprehensive platform allows for complete tracking, from the initial request submission through to voting and approval. With an intuitive, simplified process, you can review, track, and approve requestor inquiries.

Mosio allows research teams to improve subject adhesion, communications, data collection, and communication on mobile's most popular channel, text messaging. Our software helps research teams communicate more efficiently with participants by delivering interactive elements to mobile phones and messaging automation. WHO CAN WE HELP? + Clinical Trial Sponsors (Pharma & Biotech) + Cancer Centers and Clinical Research Organizations + NIH-Funded Studies + Public Health Agencies + Clinical Trial Managers/Directors and Clinical Operations Managers/Directors. Clinical Project Managers. Principal Investigators. Clinical Research (Study). Coordinators. All research staff who regularly communicate with study participants. BENEFITS + Interactive medication reminders and medication compliance alerts + Automate data collection. + Increase engagement and adherence. + Get SMS appointment reminders to fix your no-show problem. + Increase retention with automated check ins

Discover the nQuery difference today, from sample size and power analysis to adaptive trials design. The complete trial design platform that makes clinical trials more efficient, less expensive, and more successful. See why nQuery is the top choice for researchers and biostatisticians around the world who must deal with increasing trial complexity, spiralling costs, and changing regulations. Calculate the sample size required for FDA/EMA submission. Quick spreadsheet interface without any coding. Solutions for Fixed-term and Frequentist trials. All trial stakeholders can access easy-to-use reporting. Give realistic estimates of costs and timings. Align your sample size to scientific and budgetary requirements. The specify multiple factors tool allows you to fine-tune your calculations. 1000+ sample size and power calculation methods. Quickly calculate sample size in a variety of situations

Data can come at you from many directions - EDC and EHR, smartphones, mobile devices and central laboratories. Prism combines data from many sources and transforms them into information and knowledge. Prism EDC offers a new way to collect and manage clinical trial data. It combines simplicity with innovative features. Prism does more than just collect data via forms. It also aggregates and manages data coming from many sources. Prism eSource, an innovative software solution, allows researchers to extract clinical trial information directly form a site's electronic medical record (EHR). This allows for cost savings and efficiency beyond what is currently possible. It also speeds up the delivery of new therapies to patients.

eDeviation supports all operations related to Protocol Deviation management and assessment. From software design and validation to gathering supporting documents and exporting data to the TMF, eDeviation®, relieves your clinical staff from the risks of missing or incorrectly assessing protocol deviations.

The options for managing clinical trials at investigator sites were limited to either using multiple spreadsheets or purchasing expensive software that was not suitable for Australian conditions. MAISi is a game-changer. MAISi began as a repository of clinical trials data at a major medical center in 2001. It has since evolved to be a sophisticated workflow application that assists in all aspects of a research unit’s operations. MAISi is a central repository for data that stores information about studies and business units that manage them. The data are organized to support management decision making. Each business unit's staff has access to the data (Studies and Patients, Investigators, Study Teams Members) that is associated with their business unit. Staff granted global access (normally Financial officers and System Administrators) have all data access.

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

A global, infinitely scalable, AI powered, collaborative cloud platform that is globally accessible and meets the highest standards for security and compliance. A leading, easy-to-use platform for neuroscience professionals. It was designed by data scientists and neuroimaging experts to meet the unique and challenging needs of the community. Optimized for your specific needs, whether you are conducting clinical trials, designing new algorithms, or leveraging brain-related data.

The industry's best eSource, CTMS and eRegulatory software. CRIO's electronic source is the best in its class and allows you to capture source data instantly and in real time. You can eliminate up to 90% of paper and improve data quality by as much as 80%. CRIO's intuitive clinical trial management system will help you take control of your operations. You can schedule patients, track financials, streamline recruitment, and much more. Electronic regulatory binders are now ready for the 21st Century. This includes the first ever electronic delegation log, all 21 CFR Part 11 compliant. Clinical trial sponsors can now remotely monitor your sites' source data, and regulatory documents via an online portal. Join our network of 500+ clinical research sites from around the world. Our mission is to help your business grow. We help you streamline your site's operations so that your studies don’t stop because you aren’t in the clinic.

DFnet, a healthcare technology company, provides eClinical services, including electronic data capture, eSource and data management services. Our services offer greater flexibility, better data quality, as well as greater efficiency for clinical trials around the world. Collect data from any source, including paper crfs, EDC, other electronic sources, online/offline tablet, and ePRO entries. Install in your secure premises or let us host it in our secure cloud environment. Advanced optical recognition reduces the time required to perform SDV and RBM processes. For multi-center studies with maximum flexibility. Web-based data collection from any source is instantaneously available in a central real-time platform.

A simple and powerful CTMS that can be used by hospitals, site management organisations, and small CROs. It focuses on budgeting, financial tracking, and reporting. Clinicubes CTMS has many useful features that allow companies to manage and conduct clinical trials efficiently. The central management of the trial database allows for better productivity and provides more accurate information. Systematize, organize and reorganize the database of physicians and healthcare service providers. A single report will combine data from multiple studies and locations. Reporting options are available to show how the trial is performing against pre-set criteria. Interactive dashboards allow you to communicate study performance data as well as other operational reports.

The Datimbi Platform is ideal for applications that require large amounts of structured data from many collaborators. It also has built-in quality assurance controls. You can monitor and control the quality of your collection process in real time and perform reporting and analysis. You need to get things set up quickly. Our platform is optimized to handle solutions such as eCRFs in Clinical Trial Management, Social Case Management or any other workflow-driven data collection or processing. You can usually get your platform up and running in one week if your need falls within one of these categories. An easy-to-use web interface allows you to set up roles, workflow transition states, data collection forms, processing rules and lists of values, as well as custom email alerts. These tools can be managed either by your staff or via a Datimbi service.

ItemTracker is a network-enabled solution that tracks and manages all your samples. It can be used in storage, the laboratory, or anywhere else. ItemTracker users can range from small laboratories that store a few thousand samples, to larger sites that have many users and store millions of samples. ItemTracker assigns each sample a unique identifier and provides traceability and the ability for consent to be demonstrated where appropriate. ItemTracker can handle many different types of samples. You can add fields to store different information for each sample type. ItemTracker allows you to search for both the source and the sample. You can search, export to Excel, or print customized reports that only show the information you are interested in.

Dataworks Development, Inc., (Freezerworks), has been providing biobanking and sample data management software solutions since 1987. Freezerworks is an advanced LIMS for sample and study management that manages workflows from testing to billing and shipping. Secure data with the comprehensive security features and 21 CFR part 11 compliance. Labeling bar codes that are cryogenic-safe is also included. Freezerworks offers four different editions to suit your budget and needs.

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.

Qualis LIMS is an enterprise-grade laboratory information management system that is widely used in various industry verticals, such as pharmaceuticals, life sciences, contract research, clinical research, and analytical and commercial sample testing. This system has integrated modules designed to manage all laboratory processes, enabling labs to perform their tasks in an automated and paperless manner while ensuring compliance with regulatory requirements and industry standards. Qualis LIMS is a digital transformation tool for laboratories, providing the following features: • Efficient management, storage, and aliquoting of samples. • Record keeping of test and experiment results, along with the management of tests, projects, samples, instruments, and inventory in a secure central database. • Compliance with data integrity and regulatory requirements such as GxP, ISO17025, 21 CFR Part 11, and EudraLex Annex 11 without compromising quality.

Lenava LIMS software can be installed in your laboratory to ensure that every step is under control. It provides a comprehensive overview of all samples, tests, and workflows. It allows you to track all changes throughout the lifecycle of a sample and generates a detailed log of each action. Lenava LIMS (Laboratory Information Management System), which supports your laboratory in meeting customer expectations, allows you to list, track, track, develop, optimize and expand workflows, integrate reagents and consumables inventory and generate reports. Our product allows you to dynamically perform sample accessioning as well as data management, making it the core function of your laboratory software. Automate and optimize your laboratory's workflow and organize it into steps that can be tracked with features.

The most widely used LIMS (Laboratory Information Management System) is the best way to increase productivity, ensure compliance, streamline operations, and improve organizational efficiency. Thermo Scientific's SampleManager LIMS™, which combines laboratory management, data management (SDMS), and process execution/procedural ELN(LES) capabilities, is the world's most widely used LIMS. SampleManager LIMS is used by laboratories in all industries including pharmaceutical, food, beverage, oil and natural gas, manufacturing, contract testing, and water and environmental.

All aspects of your clinical trial can be managed from one platform. Zapclinica, an eClinical suite, is designed to manage and execute every aspect of your hybrid or virtual decentralized clinical trial. Automate complex processes, identify outliers and optimize resources. This will improve decision making and collaboration among sponsors, CROs, sites, and other stakeholders. Zapclinica makes it easier to manage a clinical trial. All aspects of your clinical trial can be managed from one platform. Zapclinica, an eClinical suite, is designed to manage and execute every aspect of your hybrid or virtual decentralized clinical trial. Automate complex processes, identify outliers and optimize resources. This will improve decision making and collaboration among sponsors, CROs, sites, and other stakeholders. Zapclinica makes it easier to conduct a clinical trial that is successful. All aspects of your study can be covered with one platform. You can choose the app that you need in one environment, with no additional vendors or third-party.

Create and manage containers for various entities, including samples, reagents and biologics. Inventory management is done by scanning barcodes. Create, move, split, and discard containers. Inventory's powerful search capabilities and user roles allow you to easily track hazardous compounds, regulate access and maintain laboratory safety regulations. Inventory allows the management of unique entities and reagents as well as stockroom R&D material. Reports can be generated based on the container type, sample type, container location, container status or container status. Track compound usage and set up automatic low stock alerts.

Dacima Clinical Suite, the most advanced web-based solution, combines electronic data capture (EDC), medical data management software (CDMS) and clinical trial management software into one platform. Dacima Clinical Suite is designed for clinical trials, epidemiological studies, web randomization, ePRO, surveys, and patient registers. Dacima Clinical Suite comprises three core modules: the Manager (Administrator), Designer Module, and the Data Entry Module.

OneLABz | Pathology Lab Management System. It is a web-based solution that fully automates all aspects of a pathology lab. Pathology Lab Management System Pathology Lab Management System is the most efficient, fast reporting and EMR software. Integrated web-based powerful Diagnostic Pathology Lab Management System. This system automates lab operations from sample collection to preparation of the test result. Labs can access test results online, via email, and via SMS. Pathology Lab Management System was developed for labs that need to manage patients information, employee registration, chemical stock management, fine-grained access rights, LAB expenses and collected test samples. It reduces costs, improves efficiency, increases profits, and offers flexibility. Software that integrates and coordinates all activities in the Pathology Lab.

ePharmaSolutions is building something new. We are not a high tech company. We are an idea-driven company whose thinking is deeply rooted in technology but not limited by it. We provide solutions to improve the management, activation, and training of clinical trial sites. We offer technology-enabled solutions that "un-complicate" clinical trial management. ePharmaSolutions is a leader in e-clinical solutions. Our solutions improve the selection, training, activation, and management of clinical trial sites. We bring new thinking to old problems and provide technology-enabled solutions to enable sponsors, contract research agencies, and investigator sites to "uncomplicate" clinical trial management.

Our platform provides the comprehensive support your clinical trial requires using cutting-edge cloud-hosted technology. Clinibase will make your organization more efficient and productive. Clinibase is not a plug-and play system. Why? Because every organization is unique and has its own systems and processes. Clinibase can be customized to meet your specific clinical trial requirements. We use surveys to identify areas for improvement and troubleshoot all aspects of your clinical trial processes. Our social integration tools make it easy to quickly locate and recruit eligible participants. Keep your participants engaged by providing smooth communication channels that facilitate high retention and positive participant experiences. Ensure that your trials are valid and safe by storing accurate data.

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.

The Perfect Laboratory Management System from SARU TECH is a comprehensive program designed to improve efficiency and accuracy within laboratories. It has features like real-time tracking of samples, digital entry for test results, equipment maintenance with automated alerts, and robust stock management to avoid running out. It also supports workflow optimization, compliance and regulatory management, detailed reporting, and analytics to help make informed decisions. The system ensures secure access for users and facilitates effective communication between lab personnel.

SMART-TRIAL is the best EDC platform for MedTech. Get closer to your clinical data. Complete data collection toolbox for Post-Market Clinical Follow-Up and Clinical Investigations. Built to empower clinical teams and give them full control over their clinical data, without compromising on design, compliance, or features.

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

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

Formerly eClinicalOS IBM Clinical Development is a unified cloud-based data management platform. It offers a smarter way of collecting and managing clinical data. IBM Clinical Development is a SaaS solution that allows users to access all study data and platform functions via an intuitive and simple web interface.

ClinEdge is changing the clinical trial industry through a comprehensive range of services that are tailored for sponsors, CROs, and sites. Because we understand the problems and barriers our clients face, we can creatively and collaboratively solve them. ClinEdge is committed to increasing overall trial success at every stage of every study. We provide Site and Patient Access for Sponsors/CROs, and enhanced Trial Solutions for Site partners. ClinEdge has over a decade's experience and a deep understanding about our clients and their challenges. We are committed to revolutionizing study conduct.

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.

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

With just one search, you can quickly locate any reagent in any freezer. Our powerful search engine features advanced filters, sorting, ranking, and ranking. All protocols can be created, shared, and archived from one platform. You and your team can create new experiments by using existing protocols at any moment. Are you running out of reagents? Send an order request to your lab managers and they will be notified immediately to purchase the reagents. You can use the message feature to communicate with other researchers to increase collaboration. Genemod wants you to save time, money, and effort by bringing together your teams' collective knowledge in a visual interface. Inventory management is done in one place, instead of multiple Excel sheets. To automate data entry, use bookmarks and activity logs. You will have a single trusted place for all your workflows. Every activity and sample archive is important.

Trial leaders can control the timelines and adapt to changing conditions with the eAdjudication®, software managed service. They also have the ability to monitor trends in provider performance over long trials and to ensure protocol conformity. The innovative, all-inclusive managed software service will help you avoid hidden costs and time delays in your Endpoint Adjudication Study. The eAdjudication®, Managed Software Service is the best way to manage Endpoint Adjudication. The eAdjudication® platform allows staff from Ethical, study teams, committee members, and clinical organizations to interact online in real time in a user-friendly and GxP compliant environment. This avoids manual processes that can be costly, time-consuming, expensive, and error-prone. eAdjudication®, all-inclusive services, streamline integration and adoption EA software across eClinical organisations.

CSAM Studies (previously MedSciNet Studies), is an online environment that allows for secure and highly customizable hosting of clinical trials and studies of all sizes. It has a 20-year history of hosting successful clinical trials and research of all types. Studies is a web-based platform for medical research. It offers a sophisticated online application package that allows you to host, maintain, and monitor projects of any size or complexity. The standard Studies solution from CSAM MedSciNet includes all the components necessary to set up a clinical trial or study. The benchmark solution supports rich and interactive data entry forms, flexible workflow structures, advanced data validation, analysis and exporting capabilities.

Study teams are being challenged to do more with less resources. Disconnected systems, manual data entry, redundant workflows and information silos can all lead to delays in a trial's progress. Medidata offers a clinical trial management solution that unites and streamlines workflows, while still maintaining full visibility. Rave CTMS is the only data-driven solution that enables faster, smarter, and more efficient end-to-end trial management. Medidata is an integral part the Medidata Rave Medical CloudTM. It provides all the elements you would expect from an industry-leading CTMS, and more. Rave CTMS gives your study teams the ability to plan and manage clinical trials in a consistent, harmonized way that standardizes activity management and planning at the country, site, and study levels. These activities include the creation and activation of study/site teams, patient enrollment and milestone tracking as well as site monitoring and issue management.