Alternatives to GoVal

Qualio is a purpose-built quality and compliance platform for life sciences companies operating in complex, high-stakes regulatory environments. Medical device, SaMD, biotech, and pharma teams use Qualio to replace fragmented eQMS tools, spreadsheets, and consultant-driven audits with a single, validated system that delivers continuous audit and inspection readiness. Qualio combines a modern eQMS with Compliance Intelligence—an AI-driven layer that continuously evaluates how well real operating data aligns with regulatory requirements. Instead of treating audits as one-off events, teams gain always-on visibility into compliance coverage, risk exposure, and readiness across FDA, ISO, EU MDR, GxP, and software-intensive standards. Core quality workflows—document control, training, CAPA, change management, supplier quality, and design controls—are directly connected to regulatory obligations and objective evidence. Deep integrations with Jira, Azure DevOps, GitHub, TestRail, and Salesforce automatically capture proof from development and operational systems, eliminating manual evidence gathering and reducing compliance drag on engineering teams. Compliance Intelligence runs multi-standard gap analysis in under an hour, flags emerging risks before they become findings or 483s, and maps reusable evidence across frameworks to accelerate submissions and market expansion. All insights are explainable and traceable back to specific clauses and internal policies, supporting validation and audit expectations. The result: audit readiness in weeks instead of months, fewer fire drills, faster launches, and lower long-term compliance cost. Qualio turns compliance from a reactive burden into a predictable, scalable system.

Trusted by more than 1 million users in 188 countries, MSB Docs enables organizations to easily create documents, send these to the signers for eSignatures, and archive them. MSB Docs has also been consecutively featured on Gartner's eSignature vendor, Gartner's Hype-Cycle, and Gartner's Market Guide for 5 years.

Document Control is MediaLab’s document management system. Our online solution empowers lab directors and supervisors to manage their policies, procedures, forms, job aids, and worksheets using configurable review settings, custom approval workflows, automated employee sign-offs, and more! Reduce time spent chasing approval and review signatures while benefiting from email notifications and personalized to-do lists for employees. MediaLab's Document Control supports: • Digital records and version control of all documents, • Standardization across all documents from all sites, • Electronic signatures that meet 21 CFR Part 11 standards, • Customized approval workflows and processes, • Robust searching to easily locate specific documents, and more!

Labguru, a cloud-based Electronic Lab Notebook, LIMS and Informatics Platform that offers a complete solution to life science research and industry, is secure and reliable. It records and manages laboratory data, inventory, molecular biology tools, and chemistry tools. This allows labs to run more efficiently and automates lab operations. Labguru allows scientists to design experiments and workflows. They can also capture structured and unstructured information, manage projects, and share their results. You can create custom-designed experiment templates and integrate protocols, SOPs and other cutting-edge features to improve data quality, streamline workflows, and reduce costs. Labguru is available via the cloud on desktops as well as mobile devices. Labguru is part Holtzbrinck Publishing Group. It serves more than 100,000 scientists from universities, research institutes, startups, and large pharma companies around the world.

Qualcy Biomed QMS Software was designed for Bio-Medical businesses (including Biotech and Pharma) to manage QMS records in accordance with FDA and ISO13485 requirements. * Meets 21 CFR Part 820 requirements * Features include E-sign, audit trails, and compliance with 21 CFR part 11. This software manages Doc. Change control, complaints, audits CAPA, NC Records Training Records and many more.

Validfor is a robust and secure digital validation platform that consolidates the entire validation process into a single, paperless system, specifically tailored for industries that are heavily regulated. This platform not only streamlines validation tasks but also guarantees adherence to critical standards such as GAMP 5, 21 CFR Part 11, and EU Annex 11. With capabilities for handling electronic records and advanced electronic signatures, Validfor ensures complete audit trails, role-specific workflows (including Author, Reviewer, and Approver), and thorough CSV compliance. It securely organizes all documentation and records within a centralized repository, meticulously tracking every modification to maintain data integrity and uphold Quality Assurance. Additionally, Validfor provides integrated modules for Change Management, Deviations, Testing, and Periodic Reviews, thereby facilitating smooth impact assessments, tracking of CAPA, Computer Software Assurance (CSA), and management of audit-ready lifecycles. This comprehensive approach not only enhances operational efficiency but also strengthens compliance across various validation activities.

Uncover, chart, and transition business application connections to the cloud environment. Take initiative in evaluating security threats from a business standpoint while streamlining network security policy alterations with zero manual intervention. Correlate cyber threats to business functions, ensuring a comprehensive view of security impacts. Enable the automatic discovery, mapping, and secure provisioning of network connections for business applications. Oversee both on-premise firewalls and cloud security groups through a unified interface. Streamline the process of security policy changes, encompassing everything from planning and risk assessment to execution and validation. Regularly evaluate each security policy modification to reduce risks, prevent service interruptions, and maintain compliance standards. Generate reports ready for audits automatically, significantly diminishing preparation time and expenses by as much as 80%. Additionally, refine firewall rules to enhance security while keeping business needs intact, thereby creating a more resilient operational framework. Through these measures, organizations can achieve a more integrated and secure cloud transformation strategy.

Arxspan's Electronic Lab Notebook offers a comprehensive cloud-based platform dedicated to the management of scientific data, effectively merging chemistry and biology information into a singular cohesive system. This innovative tool is meticulously crafted to foster collaboration in research between internal teams and external collaborators. It provides streamlined support for conducting chemistry and biology experiments and workflows all within a unified cloud-based ELN. Users benefit from advanced features such as keyword and chemical searching, alongside the convenience of attachment and in-line editing for various file types, including Microsoft Office documents, images, and instrument outputs. By utilizing the secure and private Arxspan Cloud environment, organizations can avoid the high costs associated with hardware procurement, ongoing maintenance, and IT management. The platform also features seamless integration with existing legacy electronic laboratory notebook systems, allowing for easy data migration. Users are afforded the flexibility to share views and contributions at both the notebook and project levels, further enhancing collaborative efforts. Additionally, Arxspan provides customizable user role and permission hierarchies, along with workflows for experiment signing and witnessing, ensuring compliance and accountability. The inclusion of SAFE BioPharma compatibility adds multi-factor authentication capabilities, enhancing security. Furthermore, the platform supports system validation and the management of system updates, ensuring that users remain compliant with industry standards and regulations. This holistic approach makes Arxspan's Electronic Lab Notebook a powerful asset for any research organization aiming to modernize its data management practices.

SciCord Solution features are designed to help your company transition quickly into the digital age. SciCord ELN/LIMS can be used to ensure compliance in both manufacturing and laboratory settings. Validated formulas can improve compliance and eliminate errors in calculation. To ensure compliance with SOPs, create lists. Automatic entry verification to flag possible Out-Of-Specification scenarios. Restrictions to prevent the use of expired solutions and ensure that equipment is only used by trained personnel. Intelligent scans alert reviewers to potential issues such as unstable balance, precision, uncalibrated equipment, and unvalidated process. Fully compliant with CFR 21 Part11, including electronic signatures. Custom parsing of attached files extracts data and records it in SciCord experiments for additional calculations and statistical analysis.

Scispot delivers a powerful lab informatics platform that transforms how life science labs operate. Through its configurable LabOS™ ecosystem, teams can select from a unified suite of tools covering ELN, LIMS, SDMS, QMS, and AI capabilities—all accessible through an intuitive no-code interface. Purpose-built for CROs, Diagnostic Labs, and Biotech R&D teams, Scispot addresses critical challenges in Sample Management, Freezer Management, and GxP Compliance. The platform seamlessly connects with 200+ lab instruments and 7,000+ applications, eliminating manual data entry while ensuring regulatory adherence. Scispot's AI-powered analytics convert experimental data into actionable insights, accelerating discovery timelines. With rapid implementation and a focus on user experience, Scispot enables 1000+ lab scientists and operators to standardize processes, maintain compliance, and focus resources on innovation rather than administrative overhead.

Cytobank serves as a cloud-driven platform that facilitates the analysis, storage, and sharing of flow and mass cytometry data. Being entirely web-based, users only need a web browser and an account to gain access, eliminating the need for any software or hardware installations, updates, or maintenance. This makes Cytobank especially suitable for individual researchers or small teams. For larger research groups, pharmaceutical and biotech research and development teams, as well as clinical research organizations, Cytobank offers a shared cloud option, while also providing a private cloud solution that allows for controlled access managed by a designated administrator. Furthermore, it supports enhanced computational capabilities, particularly for advanced functionalities like viSNE, making it a versatile tool for diverse research needs. Overall, Cytobank streamlines the process of data management and enhances collaboration among researchers.

LabSpeed™ Results Analysis software offers a unified platform for charting, reporting, exporting, monitoring, validating, sharing, and analyzing results from various laboratory instruments, ranging from portable devices to sophisticated multi-element analysis spectrometers and biotechnology tools. Users can quickly access their instrument data with minimal setup, as LabSpeed automatically manages data formats and connections. The software features an intuitive drag-and-drop interface, allowing laboratories to effortlessly create the necessary solutions for daily operations to enhance efficiency. LabSpeed is compatible with data from all kinds of analytical instruments, regardless of their complexity or type. It can be utilized at the instrument for tasks such as data review, exporting, and printing, or in an office setting for research, data analysis, and comprehensive publishing. Moreover, LabSpeed incorporates advanced functionalities and features typically found in separate software packages, including Crystal Reports®, SigmaPlot®, and InfinityQS®, thereby streamlining workflows and enhancing productivity across various laboratory environments. This comprehensive tool is designed to adapt to the changing needs of laboratories, ensuring that users can maintain high standards of accuracy and efficiency in their data management processes.

LabCollector is an all-in-one flexible and intuitive LIMS/LIS/ELN software, built to organize, centralize and track reagents, samples, tests, experiments, workflows, lab data and processes, with full ISO/FDA compliance. Connect any type and brand of instruments and build secure automation workflows to improve data integrity: Balances, Analyzers, Diagnostics and Chromatography Systems. Built around modules and add-ons enhanced with AI, LabCollector integrate with any ERP, CRM, QMS, EMR/EHR system through easy HL7/XML/CSV file exchange, API connection and data mapping. Receive alerts/notifications for your equipment (maintenance, warranty), reagents and samples (expiration, quantity).

ZenQMS is an electronic Quality Management System (eQMS) built for life sciences and GxP-regulated organizations, including biotech, pharma, CROs, and CMO/CDMO organizations. The cloud-based, AI-enabled, fully validated platform is designed for companies of all sizes to be easier to use, quicker to validate, and more effective at managing GxP activities. ZenQMS supports key quality processes, including: Document management/document control Training management and learning management Corrective and Preventive Actions Deviations, non-conformances, complaints, issues, and other quality events Change controls Audit management Critical quality workflows Supplier and vendor management Electronic signatures with 21 CFR Part 11-compliance Risk management Quality metrics tracking and reporting

AmpleLogic EDMS Software serves as a robust electronic document management solution tailored specifically for the Pharmaceutical and Biotech sectors, crafted to address the stringent cGMP requirements of the Pharma industry while ensuring compliance with both 21CFR Part 11 and EU Annex 11, effectively resolving the myriad challenges encountered by various organizations. This paperless document management system allows users to seamlessly manage and interact with all types of documents and information with ease. Key functionalities of the AmpleLogic Document Management System include document creation, review, approval, editing, document comparison, version control, and the ability to conduct parallel reviews, all designed to enhance operational efficiency and compliance. By integrating these features, AmpleLogic EDMS not only streamlines workflows but also significantly reduces the risk of errors in document handling.

Flywheel provides comprehensive data management solutions to researchers looking to improve productivity and collaboration in imaging research and clinical trials, multi-center studies, and machine learning. Flywheel provides end-to-end solutions that streamline data ingestion and curate it to common standards. We also automate processing and machine-learning pipelines. Our platform allows for secure collaboration in the life sciences, clinical, academic, as well as AI, industries. Cross-platform data and algorithm integration, secure and compliant data discovery among a global network, and cloud-scalable and on-premise computational workflows to support research and clinical applications. Flywheel is a data curation platform that supports multi-modality research. It can manage a wide range of data types, including digital pathology, imaging files, clinical EMR data and omics, as well as instruments.

Scitara DLX™ provides a swift connectivity framework suitable for any instrument found within life science laboratories, all while operating on a cloud-based platform that is both compliant and auditable. As a versatile digital data infrastructure, Scitara DLX™ facilitates connections between various instruments, resources, applications, and software utilized in the lab. The comprehensive cloud system ensures that all data sources are interconnected, promoting seamless data movement across numerous endpoints. Consequently, researchers can concentrate on their scientific endeavors instead of being bogged down by data-related challenges. Moreover, DLX intelligently curates and corrects data as it is processed, fostering the creation of accurate and well-organized data models that are essential for enhancing AI and ML systems. This robust approach plays a vital role in advancing digital transformation strategies within the pharmaceutical and biopharmaceutical sectors. By unlocking valuable insights from scientific data, the platform accelerates decision-making processes in drug discovery and development, ultimately aiding in the expedited launch of new medications into the market. Additionally, the integration of such a sophisticated infrastructure not only streamlines workflows but also enhances collaboration among researchers, paving the way for innovative solutions in the life sciences field.

Introducing IDBS Polar, the pioneering BioPharma Lifecycle Management (BPLM) platform that streamlines tedious manual operations, empowering you to carry out processes more effectively while gathering the essential data needed to speed up market entry by addressing significant hurdles in process design, optimization, scale-up, and technology transfer. This innovative platform features interactive data analytics tools, including a bioreactor comparison tool tailored for biopharma development scientists. IDBS Polar excels at securely overseeing drug progression through comprehensive workflows, seamless integration, and insightful data analysis. Its structured workflows are crafted to ease the complexities of the BioPharma Lifecycle, ensuring process-aware planning, design, and execution of complete bioprocess and analytical unit operations. Meaningful integrations enhance the relevance of your data, while rapid incorporation into your development ecosystem fosters automation and establishes a robust, process-centric data framework. In an industry where precision and efficiency are paramount, IDBS Polar stands out as a vital solution for modern biopharmaceutical development.

Achieve seamless data integration and exceptional informatics management with iLES, a comprehensive hub for communication, documentation, storage, and workflow that operates in real time for your entire organization. iLES combines the functionalities of a Lab Information System (LIMS), Electronic Lab Notebook (ELN), Scientific Data Management System (SDMS), and Data Management System (DMS) into one solution. Regardless of your lab's current digital stage or which system you're considering replacing, iLES employs vendor-neutral technologies to unify your disparate data sources. This means you will only need to work within the iLES platform to manage all lab-related tasks and communications for every user. With rapid feature releases and automated upgrades, you can enjoy the benefits of the latest advancements effortlessly. Additionally, iLES provides secure access to your information from anywhere in the world on any device with an internet connection, transforming laboratories into efficient, fully integrated paperless environments. This all-in-one approach not only streamlines operations but also enhances collaboration and productivity across your organization.

PowerSchool Employee Records is a comprehensive K-12 employee records management system designed to streamline HR processes through digital forms, workflows, and secure record storage. The platform enables employees to complete essential documents like tax forms and benefits enrollments online, reducing manual paperwork and in-person visits. It offers configurable workflows and checklists to guide the employee lifecycle from onboarding through contract renewals and offboarding. PowerSchool Employee Records features automated reminders and task tracking to keep processes on schedule, ensuring no critical documentation is missed. Its digital library and reporting tools provide administrators with real-time visibility into documentation status for audit readiness. E-signature capabilities make it easy to validate employment contracts and other forms securely. Designed specifically for the needs of education organizations, it integrates seamlessly with other PowerSchool talent management products. The solution helps districts reduce administrative burden while maintaining compliance and data security.

Researchers require effective tools for the capture, management, and sharing of their research data. Additionally, these tools must be compatible with various data storage platforms and applications, including enterprise chat systems and specialized tools such as protocols.io, along with data repositories. RSpace, recognized as the Connected electronic notebook, stands out as the sole electronic lab notebook (ELN) tailored to integrate effortlessly into the research data framework of contemporary research-intensive universities. For early-stage biotech companies, there is a pressing need to advance swiftly toward their next milestone while also systematically capturing and organizing their research data. This organization is essential not only for establishing a solid foundation for long-term intellectual property protection but also for presenting results effectively to collaborators and potential investors. By connecting with various research tools and other elements of the research ecosystem, RSpace ensures that researchers' data is not only captured but also adeptly managed, ultimately making it accessible for public viewing, querying, and reuse by others in the scientific community. This holistic approach fosters a collaborative environment, enabling greater innovation and shared knowledge across the research landscape.

Sapio Sciences focuses on making life in the lab easier and more productive for scientists and the teams that support them. Founded with deep roots in machine learning and AI, the company invested early in a modern lab platform, data architecture and user experience that could support real experimental work at scale. Today, Sapio delivers the Sapio Platform, an agentic AI lab informatics platform that is unified, configurable, low code and scalable. It brings together Sapio LIMS, the market’s most advanced and flexible LIMS for automating research, diagnostics and manufacturing, Sapio ELaiN, the third generation AI lab notebook that acts as an AI co-scientist, and Sapio Scientific Data Cloud, the scientific data unification solution with built-in data organization, search, charting and tools. Scientists and lab teams can easily configure workflows, data structures and role based screens without writing code, while agentic AI helps develop procedures, automate steps and connect and analyse results. Sapio works with leading and emerging biopharma R&D, biotech, CRO and clinical diagnostics organizations worldwide.

Streamline the entire selection process for reagents and model systems to eliminate costly inefficiencies and errors that lead to experimental failures. Accelerate project timelines by facilitating the selection of reagents and model systems in a mere 30 seconds, compared to the traditional 12-week duration. This transformation can significantly cut the hard costs associated with consumables, saving organizations millions annually. By restoring valuable research time to scientists, you can enhance the organization’s mission. Experience tangible business benefits from AI through a proven, ready-to-use application. More than 41,200 scientists across 15 of the leading 20 pharmaceutical companies, as well as over 4,450 academic institutions, leverage BenchSci’s AI-Assisted Antibody Selection to design more effective experiments, resulting in documented savings of millions per year in hard costs alone. However, it's important to note that antibodies account for only 40-50% of reagent-related failures. Access a comprehensive array of experimental evidence, along with catalog data for reagents and model systems, all within one user-friendly interface. This platform integrates real-world experiment data sourced from 11.2 million scientific publications, including those published in closed-access journals, providing an unparalleled resource for researchers. With this level of detailed information, scientists can make informed decisions that significantly enhance their research outcomes.

Pluto was founded in 2021 by the Wyss Institute of Harvard University. It has been a trusted partner for many life sciences organizations across the country, from biotech start-ups and public biopharma companies. Our cloud-based platform allows scientists to manage all their data, run bioinformatics analysis, and create interactive visualizations that are published-quality. The platform is being used for a variety of biological applications. These include preclinical and translational science research, cell and gene therapies and drug discovery and development.

Sapio Sciences delivers a cutting-edge AI-driven lab informatics platform that integrates Laboratory Information Management Systems (LIMS), Electronic Lab Notebooks (ELN), and a Scientific Data Cloud into one seamless ecosystem. It is tailored to advance scientific research, clinical diagnostics, drug discovery, and manufacturing through configurable, no-code solutions. The Sapio LIMS® automates complex workflows with full configurability, removing the need for programming. Sapio ELN® offers a flexible, adaptable electronic lab notebook that supports diverse experimental needs. The platform’s Scientific Data Cloud consolidates instrument and research data enterprise-wide, paving the way for AI-driven insights. By unifying these components, Sapio simplifies data management and boosts productivity across the lab lifecycle. The platform is accessible for a wide range of industries and research applications. It aims to reduce administrative burden and enhance collaboration within scientific teams.

StackWave offers a state-of-the-art Laboratory Information Management System (LIMS), Electronic Laboratory Notebook (ELN), and Scientific Data Management System (SDMS) designed to enhance the efficiency of laboratory operations. With StackWave’s assistance, you can streamline labor-intensive scientific tasks, allowing your team to concentrate on critical research activities. These laboratory software solutions are adaptable and suitable for organizations of various sizes and sectors. Our systems cater to an extensive array of processes, having successfully collaborated with startups in biotechnology, major pharmaceutical firms, and everything in between. By utilizing cutting-edge web, database, and software technologies, the StackWave LIMS stands out as the most advanced laboratory information management system currently on the market. Built upon StackWave’s established software framework, the LIMS guarantees the flexibility, dependability, and performance required to tackle your most challenging information management needs, ensuring your laboratory is well-equipped for future advancements. Thus, embracing StackWave’s solutions will not only enhance your laboratory's operations but also position it for long-term success in a competitive landscape.

The Drug Safety Triager, developed by Clarivate, represents an advanced pharmacovigilance tool aimed at helping life sciences organizations adhere to regulatory standards. This system, which is validated for Good Practice (GxP) compliance and prepared for audits, enhances and organizes the workflow associated with literature reviews, allowing pharmacovigilance professionals to prioritize patient safety by streamlining these processes. Fully compliant with the reporting demands of major global safety regulatory bodies, including the FDA and EMA, the Drug Safety Triager includes a comprehensive validation package with every implementation. The validation documentation is carefully constructed to meet the stringent requirements set forth by the pharmaceutical sector and health authorities. Additionally, every piece of literature referenced is subjected to a meticulous review process that ensures all user actions are recorded, creating a permanent, immutable audit trail for accountability and transparency. This innovative approach not only improves efficiency but also reinforces the commitment to maintaining high standards in patient safety and regulatory compliance.

Scilligence's Scientific Data Management System (SDMS) offers a unified data storage platform that can connect with numerous instruments and devices, enabling researchers to quickly and securely access essential information. The automation features of SDMS facilitate the collection of data from scientific tools, equipment, or devices, and the subsequent extraction of metadata into a relational database, which enhances data management efficiency and promotes cost reduction. Our system ensures rigorous version control, comprehensive audit trails, and a detailed history of document changes that comply with prevalent regulatory standards. Furthermore, SDMS not only integrates effortlessly with Scilligence applications but also works harmoniously with laboratory instruments and devices for automated data collection. Additionally, it supports the integration of various other database systems and storage options. To safeguard your intellectual property, we provide robust access management at the site, account, and project levels, ensuring that sensitive information remains protected while facilitating collaborative research efforts. This comprehensive approach to data management ultimately empowers scientists to focus on their research while relying on a secure and efficient data infrastructure.

Betteromics functions as a Private SaaS within your Virtual Private Cloud (VPC), enabling you to establish connections across all your data sources. You can reliably assess both structured and unstructured data through customizable rules, ensuring robust validation processes. Furthermore, it allows for comprehensive tracking and auditing of your data from the point of entry to analysis, maintaining complete data provenance. By employing natural language processing alongside large language models, you can extract data elements from clinical records for quality control, labeling, and analysis purposes. This platform enables rapid development and fine-tuning of models tailored to your specific tasks or datasets, allowing for anomaly detection, predictive analytics, data comprehension, and process optimization. Additionally, it enhances your analytical capabilities and machine learning endeavors by providing access to integration-ready public datasets. With clinical-grade security measures in place, including full data encryption, traceability, and role-based access controls, Betteromics ensures that your data remains secure while facilitating insightful analysis and decision-making. Ultimately, this robust solution empowers organizations to leverage their data effectively while maintaining the highest standards of compliance and security.

ReadySign is a comprehensive eSignature platform designed to streamline document signing and management for businesses of all sizes. It enables users to send, sign, and track documents quickly through features like custom templates, bulk sending, and shareable signing links. The platform provides a centralized dashboard that offers full visibility into document status, helping teams manage workflows and follow up with signers efficiently. ReadySign supports secure document storage with role-based permissions, ensuring sensitive data is protected. It also includes automated notifications and reminders to keep signing processes on track. The system allows recipients to create signatures in multiple ways, including drawing, uploading, or selecting styles. ReadySign complies with legal standards such as ESIGN and UETA, ensuring signatures are valid and enforceable. Its transparent pricing model offers unlimited documents and signatures, making it cost-effective. Integration with ContractWorks enhances document lifecycle management. Overall, ReadySign helps organizations accelerate workflows, reduce manual effort, and improve document handling efficiency.

Kivo offers an innovative solution for sponsors and CROs, providing an economical document and process management platform that enables life sciences teams to efficiently accomplish their tasks within a single, user-friendly, and compliant environment. By integrating DMS, RIM, QMS, eTMF, and eCTD functionalities, Kivo allows teams in pharmaceuticals, biotechnology, medical devices, and biologics to handle regulated documents, quality management activities, clinical trial documentation, regulatory submissions, and workflow processes without the hassle of using multiple disconnected tools. With Kivo’s Document Management System, users can manage controlled documents and automate processes while ensuring project oversight, corporate documentation, and readiness for due diligence in a centralized manner, featuring version control, collaboration tools, audit trails, search capabilities, workflow automation, and Part 11-compliant electronic signatures. Additionally, the RIM system enhances project management and correspondence, facilitates submission building and publishing handoff, provides eCTD viewing options, and streamlines dossier management and interactions with health authorities. Overall, Kivo equips life sciences teams with the necessary tools to maintain compliance and efficiency in their operations.

Agatha provides a comprehensive range of cloud-based solutions specifically designed for the life sciences sector, facilitating the centralized oversight of documents and processes related to clinical operations, quality assurance, regulatory compliance, and training activities. This platform caters to the workflows of biotech firms, pharmaceutical companies, medical device manufacturers, and contract research organizations by offering various modules, including eTMF (Inspection-Ready Master Trial File), Remote ISF (Investigator Site File) management, and tools for creating and approving standard operating procedures (SOPs) as well as managing quality documents related to CAPAs, deviations, and change controls. Additionally, Agatha enhances regulatory document handling, ensuring smooth document creation, review, approval, storage, and sharing within a single cohesive system. By promoting a paperless approach, it alleviates administrative burdens and bolsters data security, while being constructed on a global-compliance framework that meets critical standards such as 21 CFR Part 11, GDPR, and EU Annex 11. Ultimately, Agatha empowers life sciences organizations to optimize their operations and maintain compliance with industry regulations more efficiently.

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

ValGenesis's VLMS offers an extensive array of features aimed at enhancing conventional validation methods. The platform delivers a complete perspective of the validation lifecycle, equipped with a robust management system, and can seamlessly connect with current infrastructures. By utilizing paperless validation software, it automates workflows, embeds compliance protocols within these processes, and facilitates electronic signatures through swift routing and timely notifications. Users can access metrics, dashboards, and reports instantaneously, making it easier to meet audit and inspection requests with minimal strain. This not only streamlines operations but also ensures that standards are upheld, promoting consistency in requirements management, testing strategies, and risk assessment practices. Overall, VLMS is designed to optimize efficiency and reliability in validation activities.

LabLynx offers more than standard sample tracking. It is a configurable, customizable laboratory information management system that supports inventory management, document storage and chain-of custody tracking. Our solution is tailored to meet your lab's needs. Our ELab LIMS solution redefines the concept of LIMS. It is a comprehensive information management system that can be used in every industry. This user-friendly system can be customized to meet your needs. Our LIMS Add-On Solutions will help you improve your lab's efficiency. Our solutions improve the LIMS experience and help you achieve your goals.

Document control made easy. You can create, review/approve and revise documents, as well as retire them. All transactions are recorded using e-signatures, timestamps, and stored in the Audit Trail. Audits from start-to-finish The SOLABS QM10 Audit APP allows you to track and document all aspects of your audits, from planning and preparation to closing. The SOLABS QM Essentials package offers advanced reporting capabilities and intuitive reporting. Trending and tracking are critical components of any quality management system. The dashboards and reports are easy-to-use, customizable, and can be shared in the most popular formats such as Excel, PowerPoint and PDF. You can share the reports and dashboards with anyone in your organization. In a matter of seconds, you can create, schedule, monitor, and assign training. Online assessments can be used to validate the learnings of your team. You can manage all aspects of training with the SOLABS QM Training section.

The Sapio Scientific Data Cloud is an innovative scientific data management platform that intelligently consolidates and contextualizes laboratory data, assay outcomes, instrument outputs, archives, and external ELN/LIMS records into a cohesive, searchable interface that requires no programming skills. This system facilitates automated data acquisition and interpretation from more than 200 instrument adaptors, employs semantic search capabilities driven by ontological frameworks, and features integrated charting along with sophisticated neural-network analytics such as ANOVA, best-response curves, and flow-cytometry gating. Furthermore, it delivers AI-generated insights to enhance research efficiency. To ensure the protection of sensitive information, it offers secure, role-based access and comprehensive data archiving solutions, while providing interactive viewers for proteins, molecules, plasmids, and system-wide analyses that empower scientists to delve into their findings. Additionally, the seamless integration with Sapio LIMS and ELN systems ensures that data is automatically linked with relevant samples, experiments, and entities for streamlined research workflows. This powerful combination of features makes the Sapio Scientific Data Cloud an essential tool for modern laboratories.

Encipher Health is an advanced healthcare technology platform that leverages AI to streamline and automate processes such as medical coding, risk adjustment, and revenue cycle management across various medical specialties. By employing Neuro-Symbolic AI, machine learning, optical character recognition, and knowledge graph methodologies, it transforms unstructured clinical documents into precise, audit-compliant codes (CPT, ICD-10, HCC, HCPCS) while adhering to payer and CMS regulations. The platform offers a range of products, including automation for GI coding, radiology coding through Conrad AI, anesthesia coding with Sedate AI, as well as HCC and risk adjustment solutions like Cogent AI, RiskGen-Core, and RAF Totalizer, which all work together to enhance operational efficiency. Additionally, features such as E/M coding, home health coding, support for ICD-10-AM, accounts receivable follow-up, and denial resolution contribute to reducing manual labor, minimizing the risk of denials, and expediting payment processes. With real-time and retrospective workflows, seamless integration with electronic health records, MEAT-criteria validation, modifier logic, and built-in compliance safeguards, the platform ensures high levels of accuracy, alignment with regulatory standards, and readiness for audits. Ultimately, Encipher Health stands out as a transformative solution, significantly improving healthcare operations and financial outcomes for its users.

Medcurity is a HIPAA compliance platform built for healthcare. From solo practices to large health systems, Medcurity guides organizations through their Security Risk Analysis and keeps them audit-ready year-round. Trusted by 1,000+ healthcare organizations since 2018, including Temple Health, Greater Baltimore Medical Center, and Yale. What Medcurity offers: - Security Risk Analysis (SRA) aligned with current OCR standards. Guided walkthroughs cover administrative, physical, and technical safeguards. Produces an audit-ready final report with risk-stratified remediation actions that can be assigned to team members and tracked from the dashboard. Meets SRA requirements for MACRA/MIPS and Promoting Interoperability programs. - Small Practice SRA for practices with 1 to 20 employees. A simplified assessment covering all three HIPAA safeguards, starting at $499/year. - PolicyScan scans your existing policies and auto-fills SRA questions, reducing hours of manual documentation work. - Medcurity Academy HIPAA training for employees and compliance officers, with real-world scenarios and completion tracking. - Network Vulnerability Assessments with a live dashboard, Attack Path Visualization, and AD Security Configuration Analysis. - BAA management with centralized tracking and e-signature. Keep all vendor agreements in one place. - Vendor risk management to assess and track third-party compliance. - Customizable policies and procedures built from guided templates. Share them with your team and receive reminders ahead of review dates. A dedicated support team works alongside your organization throughout the year, not just at assessment time. Medcurity was founded in 2018 in Spokane, WA and serves healthcare organizations of all sizes nationwide.

Transform your Life Sciences operations by significantly enhancing the control, efficiency, and quality of your products and processes. Maintain inspection readiness consistently with our fully compliant platform, which has undergone pre-validation in line with GAMP5 standards. Gain complete oversight of your processes and documentation, allowing for perfectly customized workflows and maximized automation wherever feasible. Experience smooth operations and comprehensive traceability through our seamlessly connected modules. Our committed team is available to address any inquiries you may have at any moment. Only the finest Scilife experience meets our high standards! The Scilife platform not only streamlines but also automates and organizes every aspect of your industry, whether in Medical Devices, Pharma & Biotech, or ATMP. Click below to explore the specific Scilife modules that cater to the distinct lifecycle stages within your industry. Our software is not just equipped with all the essential quality tools you would anticipate; it also comes with numerous additional features that surpass expectations, ensuring your operations thrive. We're excited to partner with you on this transformative journey!

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.

Logilab SDMS is an established and reliable Scientific Data Management System that can capture data from any type, make, or manufacturer of analytical instrument, making it a versatile tool for scientific research and experimentation. This system allows for the capture and archiving of both instrument data and metadata to a secure and dedicated server, which serves as a single point of truth for all scientific data. Logilab SDMS has been primarily designed to capture, catalog, and archive instrument raw data and files, along with their associated metadata. The tagging system enables data to be indexed into catalogues and archived for long-term purposes, ensuring that scientific data is readily available whenever it is needed. Furthermore, with Logilab SDMS, laboratories can confidently face audits knowing that their scientific data is organized, archived, and readily available for review.

Slingshot Pharma offers a comprehensive inventory management solution tailored specifically for pharmaceutical manufacturers seeking cGMP compliance. With real-time tracking capabilities, the software ensures precise inventory accuracy and regulatory adherence throughout the manufacturing process. It helps organizations optimize their stock levels, minimize waste, and increase operational efficiency. The system’s scalable architecture supports businesses of various sizes and adapts to evolving industry standards. Designed to keep pharmaceutical operations audit-ready, Slingshot Pharma streamlines workflows and simplifies compliance reporting. Its robust technology integrates seamlessly into existing manufacturing environments. This allows manufacturers to maintain control and visibility over their inventory at all times. Slingshot Pharma empowers companies to meet stringent regulatory demands while driving productivity.

Say goodbye to traditional PDFs and switch to mobile-friendly forms to significantly boost your completion rates. HelloWorks offers an innovative eSignature solution tailored for mobile devices, allowing you to convert cumbersome PDFs into a seamless and guided experience—eliminating the need for zooming and pinching. You can effortlessly download bulk data in a CSV format or utilize our API for direct integration into your preferred storage and analysis systems. Our eSignatures comply with SOCII and GDPR standards and include court-admissible audit trails for peace of mind. Designed with a mobile-first approach, our eSignatures provide users with an easy-to-navigate process for completing and signing documents. Leverage features like conditional logic, data validation, and form mapping to enhance the form-filling experience, reducing the chances of duplicate or erroneous entries. With a variety of pre-built templates, a no-code builder, interactive previews, and team collaboration options, you can focus on sending documents rather than getting bogged down in the building process. This makes your workflow smoother and more efficient, allowing you to engage with clients more effectively.

Food Safety Plus is an economical software solution that ensures your business is always ready for audits while facilitating document management in a completely paperless environment. Crafted by experts in food safety specifically for their peers, Food Safety Plus™ offers a budget-friendly and user-friendly cloud-based platform designed to minimize compliance risks. This software serves as a vital tool for businesses striving to adhere to the latest FSMA regulations and prepare for third-party audits effectively. You can securely store your documents in the cloud and conveniently access them from any mobile device, enhancing your operational efficiency. Additionally, you can easily approve changes and receive prompt notifications regarding updates. With a specialized portal, you can oversee compliance throughout your supply chain, ensuring that all parties are aligned with the necessary standards. Furthermore, automated communications with suppliers not only streamline processes but also help in reducing operational costs. This comprehensive approach to food safety management allows businesses to focus more on their core operations while maintaining high compliance standards.