Alternatives to TruLab

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.

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.

At Komodo Health, we integrate an extensive understanding of patient interactions with cutting-edge algorithms and years of clinical knowledge to create our Healthcare Map, which offers the most accurate representation of the U.S. healthcare landscape. This Healthcare Map serves as the backbone for our comprehensive suite of software solutions, designed to help you provide exceptional value to your customers, colleagues, and patients alike. Relying solely on traditional scholarly data for strategic planning is now outdated. Our Aperture platform has been meticulously crafted to deliver unparalleled insights into clinical leadership and influence, enabling improvements in care standards where they are needed most—whether that involves the most referenced author, a prominent social media influencer, or the physician with the highest patient volume. Moreover, conventional open/sampled prescription and patient-level data often overlook critical patterns that are essential for accurately identifying individuals with complex care needs or uncommon medical conditions. By addressing these gaps, we aim to enhance patient outcomes and streamline healthcare delivery.

While most LIMS systems can take up to a year to implement, the LABTRACK LIMS can be set up in a matter of days or weeks. Its intuitive design and built-in Forms Definition, Custom Reporting Tool, and Menu Customization Module make it easy to use. The standard LIMS modules include the following functions: Login Batch and Sample Entering and printing bar codes Custom Data Entry (useful to manage inventory, training records and specifications, etc. Test and Test-Group Scheduling Login Approval Single Request Results Entry Multiple Request/Test Results Entry Automatic Spec Checking/Flagging Lab Management Approval Example Disposition Example of Location Management Test Assignment QA Approval Reports User Account Management User Role Management And our optional Stability Study Management option adds the calendaring/scheduling functionality needed for accelerated and standard shelf life testing.

Assign a distinctive identification number to each specimen while gathering pertinent clinical information. Organize specimens according to participants, protocols, departments, investigators, institutions, disease sites, anatomical locations, and other relevant categories. Segment samples into new specimens that receive new unique IDs along with their corresponding data. Ensure the tracking of each specimen from the point of collection through freezing, thawing, and eventual disposal. Maintain compliance with HIPAA regulations, allowing for data de-identification where necessary. Oversee various biospecimen repositories simultaneously. Collect specimens in accordance with protocol calendar timepoints or through a single event timepoint, as required. Additionally, keep track of and upload consent forms and other necessary documents. Create a freezer and storage container configuration that accurately reflects physical storage conditions. Generate multiple customizable reports for inventory management, quality assurance, consent documentation, manifest creation and tracking, invoice management, and more. The system should allow users to efficiently query the specimen repository for specific types of samples, enhancing usability and accessibility. Furthermore, ensure that all data is accurately recorded and easily retrievable to facilitate ongoing research and analysis.

Explore the distinct advantages of nQuery, from sample size and power analysis to innovative adaptive trial design, and experience the ultimate trial design platform that accelerates clinical trials while reducing expenses and enhancing success rates. Learn why nQuery is the preferred option for researchers and biostatisticians globally, who are faced with the challenges of growing trial complexity, escalating costs, and evolving regulations. Effortlessly calculate sample sizes for FDA and EMA submissions with our quick, spreadsheet-style interface that requires no coding skills. We cater to both Frequentist and Fixed-term trials, providing straightforward reporting for all stakeholders involved in the trial process. Gain realistic forecasts of expected timelines and costs, ensuring your sample size aligns with both scientific and financial parameters. With the ability to fine-tune calculations using the multiple factors tool, nQuery offers over 1000 procedures for sample size and power calculations, enabling you to swiftly determine sample sizes across various scenarios, ultimately streamlining your clinical research efforts. Take advantage of nQuery's comprehensive features to navigate the complexities of modern clinical trials with confidence.

Koneksa stands out as a prominent digital biomarker firm catering to the pharmaceutical and biotechnology sectors, focusing on the creation, testing, and validation of digital biomarkers that assist clients in assessing how treatments affect patients. Established in 2013, Koneksa delivers comprehensive remote clinical trial support by integrating digital health technologies, therapeutic knowledge, and swift, user-friendly remote data gathering to enhance understanding of patient health outcomes. Their innovative and validated data algorithms are designed for immediate use in treatment development initiatives, facilitating the detection of signals more rapidly than conventional methods. The company's cloud-based Software as a Service (SaaS) platform enables real-time integration of multiple endpoints, providing instant access to data and supporting informed, cost-effective decision-making early in the trial process. Additionally, this platform’s capability to gather extensive remote data at higher frequencies presents opportunities for obtaining ecologically valid measures, which can lead to a reduction in sample size while maintaining the integrity of the research. By continuously evolving their tools and methodologies, Koneksa aims to redefine how clinical trials are conducted in the modern age.

CryoTrackIMS is a comprehensive software solution tailored for various fields, including molecular biology, cell banking, cellular biology, clinical samples, biorepositories, biobanking, biochemistry, immunology, and protein laboratories, as well as high-throughput screening, quality assurance, IVF labs, and core facilities. Users can effortlessly design any box, plate, or pie layout by choosing from rows and columns or opting for a pie configuration, allowing their custom box to be generated in mere seconds for data input. Efficient inventory management of precious biological samples and specimens is essential for both fundamental research and the biotech industry. Managing extensive collections of diverse samples such as DNA, RNA, plasmids, clones, proteins, peptides, probes, antibodies, enzymes, specimens, tissues, and cell lines can often become a challenging and overwhelming endeavor that results in significant financial costs alongside frustration and wasted time. CryoTrack provides an all-encompassing solution specifically designed for laboratories within universities, clinics, biotechnology firms, and pharmaceutical organizations. This advanced software not only simplifies sample tracking but also significantly enhances lab efficiency and productivity. By streamlining the organization of critical biological materials, CryoTrackIMS empowers researchers to focus more on their experiments and less on administrative burdens.

LIMS from ABI Health simplifies the growth of your laboratory business significantly. Within just a few hours, you can establish collection and processing centers, all of which are centralized on a single platform. This allows for business expansion, increased sample processing capacity, and access to immediate reports and insights. This is a fantastic chance to rapidly scale your operations! With the batch processing feature, LIMS offers a specialized batch sheet-tracking tool that assigns one barcode to a complete batch of samples. Technicians can monitor sample handling in real-time from the moment samples are collected and assigned their barcodes through the Workflow Manager, effectively reducing wasteful idle time and eliminating confusion about sample locations. Furthermore, automation plays a crucial role in enhancing efficiency; routine and time-consuming tasks can be automated, leading to improved productivity. By integrating all devices and equipment onto a unified, secure platform, you can also remove the need for manual data transfers, streamlining your entire workflow. This comprehensive approach ensures that your lab operates at peak performance, maximizing both efficiency and accuracy.

ItemTracker serves as a comprehensive solution for managing and tracking samples across various environments, including laboratories and storage facilities. This versatile platform caters to a wide spectrum of users, from small labs with a handful of samples to large institutions managing millions. Each sample is automatically assigned a unique identifier, ensuring traceability and the capability to demonstrate consent when necessary. The system's flexibility allows it to accommodate numerous sample types, enabling users to customize fields for specific data requirements. Additionally, ItemTracker offers robust search functionality for both samples and their associated owners, allowing users to easily locate the information they need. Users can conveniently export their findings to Excel or generate tailored reports to display only the relevant data they are interested in. This makes ItemTracker not just a tracking tool, but an essential resource for effective sample management across diverse settings.

Sarjen offers a comprehensive suite of life sciences solutions designed to optimize clinical trial management and laboratory operations. BizNET streamlines early-phase trials with automation, security, and real-time monitoring, ensuring rapid, precise execution and compliance. For late-phase trials, Smart Trial Suite accelerates processes, reduces costs, and enhances patient safety through intelligent automation, real-time insights, and extensive modules like eTMF and eDC. Complementing these, the Bioanalytical LIMS automates lab workflows, ensuring data integrity, reducing errors, and accelerating data validation for regulated environments. Together, these GxP-compliant, audit-ready platforms boost productivity, ensure regulatory adherence, and drive efficient, high-quality outcomes across the entire drug development lifecycle.

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.

By utilizing Lenava LIMS software in your laboratory, every single aspect of your operations remains meticulously managed. It offers an all-encompassing and unified perspective on samples, tests, and workflows, ensuring nothing is overlooked. Furthermore, it allows for real-time monitoring of modifications throughout the sample's lifecycle and keeps an extensive log of every action taken on it. Key features include tracking sample locations, managing inventories of reagents and consumables, integrating instruments, and facilitating the development and enhancement of workflows. Its high configurability and modularity, paired with robust report generation capabilities, empower your laboratory to exceed customer expectations. With our solution, you can actively manage sample accessioning and data handling as fundamental components of your laboratory's software suite. Additionally, you can introduce automation and streamline your processes, transforming any scientific workflow into a series of manageable and trackable steps. This ensures that your laboratory operates efficiently and effectively, consistently delivering outstanding results.

Looking for an easy-to-use lab sample management tool? This software installs directly on your local computer, with the database also housed locally for optimal control. It effectively tracks sample locations and maintains reference data, while allowing for customizable data labels. The system includes inventory management capabilities and comprehensive reporting features that can accommodate any type of plate or container. To ensure compliance, it also provides an audit trail, and offers optional barcode reader integration. Users can conveniently import data from Excel and various other applications, as well as attach documents to each sample, container, and freezer record. Additionally, support is available through phone, email, and screen sharing to assist with any inquiries. This all-in-one solution is designed to enhance the efficiency and organization of your lab operations.

PASS software offers tools for calculating sample sizes across more than 1100 statistical tests and confidence interval scenarios, which is significantly greater than what any other sample size software can provide. Each of these tools has undergone rigorous validation through published research and established texts. You can familiarize yourself with PASS by trying out a free trial, watching the accompanying video, or navigating through this website. With over 25 years of refinement, PASS has established itself as the top choice for sample size software in clinical trials, pharmaceuticals, and various medical research applications. Moreover, it has gained recognition across numerous other domains where sample size assessment is crucial. In just a few simple steps, PASS enables you to determine the sample size required for a statistical test or confidence interval. Should you require assistance at any stage, PASS provides comprehensive documentation, access to free training videos, and the option to reach out to our team of expert Ph.D. statisticians for support. This commitment to user support ensures that all users can effectively utilize the software to meet their research needs.

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.

Novatek's Clinical Assay Management software stands out as an innovative information management solution that ensures a standardized method for gathering, overseeing, and maintaining the reliability of clinical research study data. This software meticulously monitors and organizes all sample information throughout the entire analytical workflow, guaranteeing a singular, verifiable version of all clinical and analytical datasets. Furthermore, Novatek's software assists organizations in managing their studies focused on specific products under development, while also providing the necessary framework for clinical trials to ensure that all associated steps are carried out efficiently and on schedule. By facilitating improved organization and follow-through, this application ultimately enhances the quality and effectiveness of clinical research endeavors.

Mosaic from Cenevo is the leading sample management solution for life sciences, supporting organizations across pharmaceuticals, biopharma, agroscience, CROs, and not-for-profits. It centralizes the tracking, storage, and handling of diverse biological and chemical samples—including compounds, reagents, cell lines, DNA, proteins, and tissues—within a secure, auditable system. Built on over 20 years of domain expertise, Mosaic replaces manual tracking and disconnected tools with automated workflows that enhance data accuracy, reproducibility, and regulatory compliance. Its robust audit trails and sample histories allow labs to confidently trace experiments, ensuring transparency for both research and client communications. The platform integrates seamlessly with leading laboratory instruments, robotics, and informatics systems to support high-throughput environments. With over 150 global implementations and more than one billion samples managed, Mosaic is trusted by small biotech labs and large pharmaceutical enterprises alike. Its flexible modular architecture and mobile compatibility provide scalability for both evolving and enterprise-scale operations. Mosaic empowers laboratories to optimize efficiency, reduce errors, and make data-driven decisions with confidence.

Azenta Life Sciences delivers versatile, robust, and scalable informatics solutions for sample processing, allowing laboratories to effectively implement systems across various locations while leveraging integrated project and diagnostic management capabilities. Our unmatched sample exploration and management tools are designed to expedite your processes in discovery, development, and delivery. Additionally, Azenta Life Sciences provides cloud-driven informatics solutions that streamline laboratory workflows and enhance staff efficiency through standardized procedures. The software encompasses various modules that oversee clinical trials, patients and families, informed consent, storage, diagnostics, next-generation sequencing, and sample handling. It also features connectivity with external data sources and offers adaptable options for incorporating third-party systems and instruments, ensuring a comprehensive approach to laboratory management. This enables laboratories to maintain a high level of accuracy and efficiency in their operations.

Enhance productivity, maintain regulatory compliance, optimize workflows, and boost organizational effectiveness with the leading Laboratory Information Management System (LIMS) available globally. Thermo Scientific™ SampleManager LIMS™ provides an all-in-one solution for laboratory oversight, data handling, scientific data management systems (SDMS), and procedural execution through electronic laboratory notebooks (ELN). This versatile tool is trusted by laboratories in various sectors such as pharmaceuticals, food and beverage, oil and gas, petrochemicals, environmental monitoring, manufacturing, and contract testing, enabling them to fully harness the potential of their laboratory data for better decision-making and operational success. By adopting SampleManager LIMS, organizations can expect a significant transformation in how they manage and analyze their laboratory workflows.

Progressing artificial intelligence to remove the need for trial and error in healthcare, our digital twins facilitate swift and assured clinical trials. We focus on areas such as neuroscience, immunology, and metabolic diseases, among others. TwinRCTs expedite full enrollment by requiring fewer participants to provide equivalent statistical power compared to conventional trial methodologies. This approach significantly reduces the time needed for late-stage study enrollment. Additionally, TwinRCTs enhance the ability to detect treatment effects in early-stage studies by bolstering statistical power without necessitating an increase in participant numbers. They enable researchers to make informed decisions based on initial study outcomes and help attract more participants to trials. By utilizing smaller control groups, TwinRCTs also improve participants' odds of receiving the experimental treatment. Our commitment to positioning clinical trials with digital twins for regulatory success is unwavering. Unlearn is at the forefront of transforming the medical field through the innovative application of artificial intelligence, creating and implementing novel generative models that are trained on vast datasets derived from previous patient studies. This evolution in methodology not only streamlines research but also enhances the overall effectiveness of clinical trials.

Administer and oversee a variety of containers that hold samples, reagents, biologics, 96-well plates, and small molecules. Manage inventory effortlessly by using barcode scanning; options include creating, relocating, utilizing, splitting, and disposing of containers. The system’s user role features and robust search capabilities enable efficient tracking of hazardous materials, control of user permissions, and adherence to laboratory safety regulations. Inventory facilitates the management of distinct entities, reagents, and research materials in the stockroom. Additionally, generate detailed reports categorized by container or sample type, status, or location. Monitor the usage of compounds and set up automated notifications for low-stock levels, ensuring you never run out of essential materials. This comprehensive approach enhances operational efficiency and promotes a safer laboratory environment.

OneLABz is a comprehensive management system designed specifically for pathology labs. This web-based platform streamlines all laboratory operations, ensuring full automation from the moment a sample is collected to the delivery of test results online, via email, or SMS. The Pathology Lab Management System prioritizes efficiency with rapid reporting and electronic medical record capabilities. It features a robust and secure interface that facilitates the management of patient details, doctor and employee registrations, automated chemical stock oversight, and user access controls. Additionally, it tracks lab expenses, collected samples, and generates various reports, ultimately enhancing transparency and profitability. By utilizing this software, pathology labs can significantly reduce costs and improve their overall operational efficiency, ensuring a seamless integration of all lab activities. This innovative solution not only benefits lab staff but also enhances the patient experience by providing timely and accurate results.

SampleHQ is an innovative sample management platform designed specifically for manufacturers of packaging and labels. It streamlines the entire sample request process, from inception to delivery, eliminating the need for cumbersome email exchanges, spreadsheets, or manual transfers. By offering real-time order tracking, team assignments, a unified sample library, and a comprehensive activity log, SampleHQ ensures complete transparency throughout the sample workflow. Additionally, the platform seamlessly integrates with HubSpot and Salesforce, enabling suppliers to link each sample to customer records and gain insights into which requests contribute to revenue generation. By enhancing collaboration among sales, marketing, and fulfillment teams, SampleHQ not only reduces turnaround times but also guarantees a dependable and consistent delivery of samples. This efficiency ultimately fosters stronger relationships between suppliers and customers, leading to increased satisfaction on both ends.

Replior is a pioneering company specializing in software solutions for clinical trials, featuring an integrated platform that encompasses EDC, eConsent, ePRO, and Virtual Visits to enhance trial execution. Our comprehensive system, known as Trial Online, facilitates the seamless collection and management of data from investigators, participants, and wearable devices in an efficient manner. It is designed to accommodate decentralized clinical trials (DCT), allowing for flexibility with site visits, remote interactions, or a combination of both. Our journey commenced two decades ago when we were approached to create an online CRF service for a major pharmaceutical firm, marking our transition from an IT operations provider to a dedicated software developer for clinical data collection. Over the years, we have expanded our offerings to include a complete suite of data collection services, while our IT operations are expertly managed by our highly qualified sister company, Complior. As we continue to innovate, our commitment to enhancing clinical trial processes remains at the forefront of our mission.

The in-system protocol serves as a comprehensive training program, integrated with fingerprint attendance for enhanced security. Cronos offers highly customizable workflows tailored for conducting various studies such as dermal, patch, and other bioavailability-bioequivalence (BA-BE) or early-phase research. It enables the capture, cleansing, and efficient management of study data, whether sourced from paper-based or electronic data capture (EDC) trials. Additionally, users can extract data into preferred datasets in compliance with industry standards like CDISC (SDTM). The EDC tool features real-time activity monitoring, and its Bedside Data Collection capabilities facilitate quicker, paperless assessments. Furthermore, Cronos includes a sample inventory and tracking system, ensuring a compliance-ready data repository. It supports data e-printing from nearly all BA instruments and software, along with an online review process complete with e-stamping and e-signatures within a defined workflow. Users can view projects, export, and archive data efficiently while generating high-quality statistical reports, tables, listings, and formats in both fixed and customizable layouts with remarkable ease. This robust system not only streamlines the research process but also enhances overall data integrity and accessibility.

Speeding up the creation of crucial medications and ensuring that patients worldwide can access top-notch cancer treatment and research equally. Our technology is transforming how patients access cutting-edge medicines and participate in clinical trials. FICS is a groundbreaking software solution that facilitates the gathering of regulatory-compliant data throughout patient treatment. By integrating previously isolated and non-interacting applications into a comprehensive, seamless platform, FICS is making clinical trials more efficient, quicker, and of superior quality, ultimately enhancing patient outcomes in significant ways.

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

AssisTek stands out as a frontrunner in cutting-edge clinical technology solutions tailored for clinical research, providing specialized software that optimizes and improves the process of gathering patient data. With a legacy of over 25 years, the company has successfully facilitated more than 800 clinical research trials spanning 46 therapeutic areas, which include upwards of 500 multinational Phase I–IV clinical trials. Their electronic Clinical Outcome Assessment (eCOA) solutions boast scalability, customization, and efficiency, backed by a reliable cloud-based technology platform. Among their extensive product offerings are the TEK eCOA Tablet, which accommodates any questionnaire utilized in clinical trials, TEK eDiary, enabling the collection of patient-reported outcomes from home, TEK Configurator for comprehensive project development in clinical trials, and TEK Study Portal, which consolidates eClinical tracking, training, and reporting into one convenient location. AssisTek's innovative systems and services have established them as the preferred partner for data collection and analytics, winning the trust of both patients and healthcare professionals alike. As they continue to evolve, AssisTek remains committed to enhancing the efficiency and accuracy of clinical research methodologies.

Sano Genetics delivers a comprehensive 360° platform designed for precision medicine and clinical trial research, integrating various aspects such as patient recruitment, genetic testing, informed consent, and ongoing engagement to significantly enhance and streamline study processes. The platform accommodates custom protocol creation and the preparation of ethical submission documents, alongside digital prescreening and consent procedures, as well as recruitment assistance through online marketing efforts, partnerships, and advocacy groups, which allows sponsors and contract research organizations to connect with specific patient populations or those often overlooked in various regions. Additionally, Sano provides convenient, non-invasive saliva-based DNA testing kits that serve as a budget-friendly option compared to traditional clinic blood draws, along with logistical support for sample collection and processing. Their services include dependable genetic and biomarker analysis conducted by accredited laboratories, bioinformatics services, and the return of results, complemented by genetic counseling when necessary, ensuring a holistic approach to patient care and study accuracy. By leveraging technology and community engagement, Sano Genetics is poised to transform the landscape of clinical trials and personalized medicine.

Illuminate the black box and install 3LC to acquire the insights necessary for implementing impactful modifications to your models in no time. Eliminate uncertainty from the training process and enable rapid iterations. Gather metrics for each sample and view them directly in your browser. Scrutinize your training process and address any problems within your dataset. Engage in model-driven, interactive data debugging and improvements. Identify crucial or underperforming samples to comprehend what works well and where your model encounters difficulties. Enhance your model in various ways by adjusting the weight of your data. Apply minimal, non-intrusive edits to individual samples or in bulk. Keep a record of all alterations and revert to earlier versions whenever needed. Explore beyond conventional experiment tracking with metrics that are specific to each sample and epoch, along with detailed data monitoring. Consolidate metrics based on sample characteristics instead of merely by epoch to uncover subtle trends. Connect each training session to a particular dataset version to ensure complete reproducibility. By doing so, you can create a more robust and responsive model that evolves continuously.

At ePharmaSolutions, we are pioneering innovative approaches. While we don't classify ourselves as a high-tech firm, our foundation is built on ideas that are deeply rooted in technology yet not confined by it. We enhance the drug development landscape by offering solutions that streamline the processes of identifying, activating, training, and managing clinical trial sites. By viewing traditional challenges through a new lens, we provide technology-driven solutions designed to simplify the complexities of clinical trial management. ePharmaSolutions (ePS) stands out as a premier provider of e-clinical solutions that transform the methods of selecting, training, activating, and overseeing clinical trial sites. By infusing fresh perspectives into longstanding issues, we create innovative, technology-facilitated solutions that enable sponsors, contract research organizations, and investigator sites to effectively navigate and simplify the intricacies of clinical trial management. Our commitment to redefining these processes ensures that we remain at the forefront of the industry, continually adapting to meet evolving needs.

AcceleTrial™ eliminates uncertainties in identifying and activating clinical trial sites. Our Study Start-up Management System (SSMS) relies on objective data rather than self-reported information. With AcceleTrial™, you gain access to a comprehensive database of thousands of globally ranked and indexed sites, evaluated based on their specific therapeutic expertise, clinical trial experience, and patient data. This system allows for an objective pairing of the most suitable sites worldwide with the relevant data on expertise, experience, and patient demographics for your clinical trials. You can swiftly engage the right sites to commence patient enrollment through AcceleTrial™'s automated “push and pull” functionality, available in multiple languages. The platform simplifies the process of gathering necessary documents with pre-filled templates and enables real-time tracking of activities. You can begin utilizing the system immediately, as it is a cloud-based solution that requires minimal IT infrastructure or training. Moreover, AcceleTrial™ can be seamlessly integrated with CTMS or other existing clinical trial management systems for enhanced efficiency. This ensures a streamlined approach to clinical trial management, allowing researchers to focus on their core objectives.

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.

The IVFID system serves as a cutting-edge security measure tailored for IVF clinics, ensuring accurate matching and verification of sperm, oocyte, and embryo samples throughout the entire IVF treatment journey. By utilizing Radio Frequency Identification (RFID) technology, it meticulously monitors and authenticates samples at each critical phase, including sperm and oocyte collection, tracking, Intracytoplasmic Sperm Injection (ICSI), embryo transfer, and cryopreservation processes. At the start of their treatment, patients are provided with wristbands embedded with RFID chips, while all consumables, such as test tubes and cryotopes, are equipped with disposable RFID tags that feature the names and patient numbers of both the patient and their partner. The system operates wirelessly to confirm all actions performed in laboratory and surgical environments, capturing comprehensive operational data, including the names of procedures, involved personnel, time and date, and exact location of the processes. In order to safeguard against sample discrepancies, the system automatically engages a locking mechanism to prevent any unauthorized access or errors. This innovative approach not only enhances security but also instills greater confidence in patients undergoing IVF treatments.

EDMS enhances the efficiency and cost-effectiveness of environmental data collection, management, and reporting while ensuring standardization across the board. By establishing a clear, documented, and auditable procedure for collecting, storing, and reporting environmental data, it streamlines the entire process. All phases of sampling and analysis are meticulously tracked, and the system is capable of sending notifications via email or SMS for various purposes. Automatic alerts are generated for instances of non-compliance and sample exceedances, further enhancing accountability. The initial phase of any environmental field initiative involves careful scheduling and planning of sampling events, which EDMS facilitates by enabling project managers to design, assign, and oversee these events. These sampling events can be organized as one-time occurrences or scheduled regularly. Before data collection begins, project managers can identify sampling stations, which come with detailed information about their locations, construction, sampling defaults and methodologies, required laboratory analyses, necessary equipment, and personnel involved. By incorporating these features, EDMS not only simplifies the process but also ensures that all stakeholders are well-informed and prepared for successful data collection.

BioShare serves as a dedicated platform where researchers can efficiently search for available collections and submit their requests for specimens and relevant data. Additionally, it offers a well-organized system to oversee the request and approval processes, ensuring seamless communication throughout. At BSI Systems, we advocate for the shareability of data to enhance the quality and efficiency of research collaborations between laboratories. As a web-based resource, BioShare enables the sharing of biospecimens and datasets within the research community, making it easier for scientists to connect. Researchers benefit from a centralized hub where they can search, submit requests, and monitor all interactions related to their requests. The platform features a user-friendly interface that simplifies lab sample tracking, making the process more accessible than ever. With BioShare, the complexities of tracking specimen and data requests have been significantly reduced, allowing for complete oversight from the moment of request submission through to the voting and approval stages. The intuitive, streamlined process enhances the ability to review, track, and approve requests, ensuring a more efficient experience for all users. BioShare truly revolutionizes how researchers manage their requests and collaborations in the scientific community.

Emergent Drums 2 represents a groundbreaking advancement in music production, utilizing artificial intelligence to create an endless array of drum samples. Our state-of-the-art generative algorithms are meticulously crafted to produce unique drum sounds from the ground up, ensuring that every sample is entirely one-of-a-kind as they do not rely on any pre-existing recordings. By leveraging our innovative deep sampling technology, users can effortlessly generate countless variations from their own sample libraries; all it takes is to import a sample, adjust the similarity slider, and press generate for limitless creative possibilities. This plugin includes two distinct infinite sound models: Creamy, which showcases exquisite, glistening cymbals, robust and resonant kicks, along with snappy snares, and Crunchy, offering a high-octane array of gritty, noisy drums infused with glitches for a truly experimental vibe. Both models can be combined to create your ideal drum kit. Beyond merely functioning as a sample generator, Emergent Drums 2 is a comprehensive 16-pad instrument that can be easily played via MIDI, featuring support for multiple outputs, making it an essential tool for any music producer. With its versatility and innovative features, it opens up endless avenues for creativity and exploration in sound design.

SampleTron 2 merges the renowned sound engine of IK's acclaimed SampleTank 4 with cutting-edge tape modeling technology to faithfully reproduce the iconic, rich sounds of tape samplers from the 1960s and 1970s, in addition to the unique tones of early digital sample players and vocoders. This extensive library includes meticulously sampled vintage Mellotron® and Chamberlin tapes, a selection of newly recorded acoustic sounds processed with tape effects, and the innovative capability to import your own samples, allowing you to craft personalized audiophile Tron sounds. With 8GB of virtual instrument assets, it boasts an impressive array of vintage and tape-based samplers. The collection offers over 400 tracks sampled from legendary instruments like Mellotrons, Chamberlins, and Optigans, allowing each preset to utilize three tracks for splitting, layering, and soloing from this vast library. Additionally, it features a variety of modern non-Tron instruments alongside its rich collection of vintage digital samples, ensuring a diverse sonic palette for all creators.

IVR Clinical Concepts is a company that focuses on offering technology for virtual clinical trials and solutions for patient engagement. Their products feature electronic patient-reported outcomes and patient diaries, which are designed to enhance data quality by minimizing errors, thereby shortening timelines and reducing overall costs. Furthermore, they provide comprehensive patient recruitment and outreach services that emphasize outreach, pre-screening, and the collection of real-time data. The solutions for subject screening, registration, and randomization are characterized as modular, tailored, adaptable, and customizable. In addition to these services, IVRCC also delivers clinical trial material management solutions aimed at lightening the workload while ensuring greater control, along with eClinical integration services that work to unify data seamlessly. Their chart review services offer insights based on real-world data and clinical experiences. By prioritizing custom, modular, and adaptable solutions, IVRCC strives to enhance the patient experience and maximize the success rates of clinical trials. This commitment to innovation positions IVRCC as a leader in the industry, dedicated to improving the efficacy of clinical research.

Data flows in from various channels, including EDC, EHR, smartphones, mobile devices, and central laboratories. Prism expertly integrates this diverse information and transforms it into usable knowledge. By combining user-friendliness with cutting-edge features, Prism EDC presents a modern approach to collecting and managing clinical trial data. Beyond traditional form-based data gathering, Prism also consolidates and organizes information from a wide range of sources. Additionally, Prism eSource offers a groundbreaking software solution that enables research teams to directly pull clinical trial data from a site's electronic health record (EHR). This innovation not only enhances efficiency and reduces costs compared to the existing model—where sites redundantly input the same data into multiple systems—but also speeds up the availability of new therapies to patients in need. As a result, the healthcare industry stands to benefit significantly from the streamlined processes that Prism facilitates.

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

At Calyx, we understand that the foundation of a successful clinical development initiative lies in the quality of your data, which underscores the importance of an efficient electronic data collection (EDC) system. Employed in over 2,600 clinical trials globally, Calyx EDC facilitates the streamlined collection and reporting of clinical trial data through a user-friendly platform. It’s essential to safeguard your critical data with a reliable partner—reach out to us to discover how Calyx can enhance the success of your program. With Calyx EDC, you gain the adaptability to effortlessly plan, design, and execute studies of any complexity. Its features are crafted to lower costs, enhance site visibility, and boost efficiency, ensuring your trial remains on course. Trust Calyx to be the ally you need for navigating the complexities of clinical trials.

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.

Omda MedSciNet solutions enhance the quality, usability, and administration of medical data throughout its lifecycle from collection to analysis. This secure and standardized software streamlines the process for clinical researchers and other professionals in healthcare and academia, allowing for the efficient gathering and examination of well-organized medical data. The dedicated Omda team excels in the development and management of customized database applications, as well as designing clinical studies tailored for medical research and quality registries. The Omda MedSciNet study platform offers a dependable, feature-rich, and highly adaptable online environment suitable for hosting and managing complex study and clinical trial systems. With a proven track record spanning 20 years, Omda MedSciNet has effectively supported studies and clinical trials of various scopes and sizes. Standard implementations come equipped with a comprehensive array of components essential for launching fully functional studies or clinical trials, ensuring that researchers have all the necessary tools at their disposal. This commitment to quality and customization positions Omda MedSciNet as a leader in the field of medical data management.