Alternatives to Kneat Gx

Interfacing’s Integrated Management System (IMS ) is an AI-supported platform that brings BPM, QMS, Document Control, and GRC together in one environment. Teams use IMS to design and manage processes, govern documentation, oversee risks, and demonstrate compliance with complete visibility and reliable audit evidence. Built for sectors that depend on strict oversight, such as aerospace, life sciences, public sector, and financial services, IMS offers real-time monitoring, automated workflows, and AI-driven analytics that strengthen quality and lower operational exposure. The system is ISO 27001 certified and validated for 21 CFR Part 11, ensuring secure and compliant use in regulated operations. IMS also provides low-code automation, process mining, audit tools, training management, CAPA workflows, and dashboards that help organizations improve performance and maintain regulatory control. AI enhances governance, improves precision, and supports continuous compliance.

Sign electronically with Skribble Legally valid all over the world, securely hosted in Switzerland. Commonly used for: Annual financial statements, sales contracts, employment contracts. This is the easiest way to legally sign documents without any formal requirements. Upload documents. Upload the PDF document directly from browser or use Skribble via API in your business software. Invite signers. Invite signatories from both internal and outside by e mail. Select the eSignature standard to be used for signature. You can sign at the touch of a button. Sign legally in compliance with EU and Swiss law on your smartphone or computer in just seconds. Skribble allows you to sign electronically and save 90% over signing on paper Take advantage of the benefits of seamless digital processes. Sign contracts faster. All parties can quickly access the latest version of the contract within seconds and sign it in just a few clicks.

SimplerQMS is an expert-driven electronic Quality Management System (eQMS) purpose-built for Life Science organizations. Our eQMS is designed by professionals with deep industry experience and supports compliance with FDA, ISO, and GxP requirements through automated, audit-ready quality processes. The platform centralizes and automates core quality workflows within a cloud-based, fully validated system. Customers benefit from reduced manual work, fewer errors, and consistently organized, inspection-ready records. Unlike generic QMS tools, SimplerQMS comes pre-configured for Life Science needs, with built-in templates, workflows, and controls aligned with FDA 21 CFR Part 11, 210/211, 820, EU Annex 11, ISO 13485:2016, and other applicable standards. Beyond software, customers gain a trusted partner backed by deep regulatory and quality expertise. This includes: • Audit-proven insights • Guidance from compliance specialists • Continuous system validation • User training • 24/7 global support • Smooth implementation and data migration • Dedicated Customer Success Experts With a mission to help Life Science companies manage quality and regulatory documentation efficiently, SimplerQMS supports organizations from early-stage growth to global scale to strengthen compliance, operational control, and quality culture.

Res_Q is an AI-powered electronic validation platform designed to help life sciences organizations manage computerized system validation and regulatory compliance. Developed by Sware, the cloud-based software centralizes validation planning, documentation, execution, approvals, and ongoing lifecycle management. Its agentic AI capabilities automate administrative activities, monitor validation progress, and identify milestones that require review or intervention. Intelligent risk assessment tools evaluate system criticality to prioritize validation workloads and support risk-based compliance strategies. The platform includes automated document processing that converts uploaded validation materials, vendor manuals, and supporting records into organized, searchable information. Its video-to-script functionality transforms recorded software processes into structured validation test scripts. Smart dashboards provide visibility into validation status, operational performance, outstanding tasks, and compliance activities across multiple systems and locations. Res_Q supports GCP, GLP, GMP, and AI validation workflows, including risk-based documentation and change management aligned with GAMP 5 principles. Through Res_Q Connect, organizations can integrate applications such as Jira and ServiceNow, coordinate automated testing, and maintain audit trails across connected systems.

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.

GoVal is an AI-powered validation software purpose-built to digitize the full validation lifecycle across pharma, biotech, medical device, and other life science industries. From Computer System Validation (CSV), Equipment Qualification, and various validation requirements to broader GxP compliance needs, it leverages intelligent automation to deliver streamlined digital workflows—all within a secure, paperless framework. Its customizable platform with role-based workflows enables automated reviews, approvals, and real-time visibility, backed by compliant e-signatures and audit-ready traceability. Built to meet 21 CFR Part 11, EU Annex 11, and leading GxP standards, GoVal ensures seamless regulatory alignment. Risk-based strategies at the URS level empower teams to drive targeted mitigation planning and precise test case design. GoVal AI goes further—accelerating validation timelines through generative assistance for risk assessments, documentation, and test development. An in-built Document Management System (DMS) allows users to securely store, organize, and retrieve validation documents as needed—supporting data integrity, traceability, and effortless access during audits. Integrated deviation management, change tracking, and continuously updated data simplify inspections while reducing manual errors. The result: faster deployment, lower compliance costs, and stronger ROI—delivered with clarity, control, and continuous compliance.

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.

TestFlow serves as a comprehensive platform for automating electronics testing, catering specifically to teams involved in hardware validation and test systems. By allowing users to describe their desired tests, the AI agent efficiently generates a workflow and Python scripts that facilitate the control of compatible lab instruments using VISA and SCPI protocols. The application runs tests directly from a Windows desktop, systematically logs measurements against predefined limits, and compiles detailed reports based on the outcomes. Users can not only reuse and manage versions of their workflows but also plan their validation processes directly from datasheets and import sequences from NI TestStand. The platform features a browser-based workspace that enables both the construction and simulation of tests, while the desktop application seamlessly connects to bench instruments for execution. TestFlow is specifically designed to support teams in the fields of electronics, embedded hardware, and validation, encompassing test-system integrators who frequently handle diverse instrument configurations from various vendors. This versatility ensures that TestFlow remains an essential tool for enhancing efficiency and accuracy in electronic testing environments.

Tricentis Vera redefines Digital Validation by going beyond merely affixing electronic signatures to digital documents, instead revolutionizing the Computer Systems Validation process to eliminate cumbersome and unnecessary documentation practices while ensuring compliance is inherently linked to robust software quality measures. By integrating triggers and controls for capturing electronic signatures that comply with 21 CFR Part 11 into Agile software testing workflows, organizations can significantly hasten their time to market with Tricentis Vera. Additionally, Vera offers a unified interface across various tools, serving as a comprehensive system of record that allows users and teams to monitor their review and approval processes in real-time. After validation assets are either submitted for approval or receive the necessary endorsements, the records are securely locked in both qTest and Jira, preventing any alterations during or after the approval phase. This seamless integration ultimately enhances collaboration and streamlines workflows, ensuring that quality and compliance are maintained throughout the software development lifecycle.

Orcanos is an integrated MedTech software platform built to help medical device companies manage quality, compliance, product development, and regulatory documentation from one connected workspace. It combines electronic quality management, application lifecycle management, design controls, document control, risk management, traceability, and audit readiness. The platform is designed to bridge the gap between R&D and Quality teams by connecting user needs, requirements, hazards, mitigations, tests, validations, complaints, and quality processes. Orcanos supports regulated frameworks and standards such as ISO 13485, EU MDR, ISO 14971, FDA requirements, and 21 CFR Part 11. Its eQMS capabilities include document workflows, PDF publishing, revision control, electronic signatures, training automation, audit trails, CAPA support, and quality process management. ALM and design control features help teams maintain a live digital thread across development artifacts, risk files, verification activities, and design history documentation. Orcanos also offers customizable no-code workflows, configurable fields, granular permissions, and migration support for teams moving from spreadsheets or legacy tools. Its AI-powered assistant, Ask Paul, is positioned to help users navigate operations and improve efficiency. By unifying quality and development data, Orcanos helps medical device organizations stay audit-ready while reducing manual documentation work.

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.

ClearWork is an AI-powered automated discovery platform that eliminates the bottleneck between stakeholder knowledge and client deliverables — built for consulting firms and internal operational excellence teams running complex transformation engagements. Most discovery tools produce a snapshot. ClearWork produces something different: a living, structured knowledge base that updates as new sources are incorporated. AI-guided asynchronous interviews gather structured input from stakeholders at scale — voice and text — without requiring a consultant in the room. Every response is automatically synthesized and reconciled against the existing knowledge base, with proposed changes surfaced to human reviewers before they're accepted. The result is a system of record you can trust, not just a faster way to generate documents. From that validated base, ClearWork automatically generates the full discovery stack: process maps, requirements documents, standard operating procedures, and requirements traceability matrices — all linked to source, all updated when the underlying knowledge changes. Scope drift that would surface as a surprise in implementation is detected the moment it enters the system. For consulting firms, this means compressed timelines, standardized knowledge capture across project teams, and deliverables that stay current. For internal transformation teams doing business process mapping at scale, it means institutional knowledge that doesn't walk out the door. ClearWork is the transformation intelligence layer between what stakeholders know and what clients receive.

FAD® serves as a digital signature on electronic platforms, mirroring the function of a traditional handwritten signature on paper while incorporating robust preventive and security technologies. This platform facilitates remote identity verification and multimedia signatures, actively combating identity theft and fostering both democracy and financial inclusion, thereby ensuring the reliability of all documented agreements. It enables the validation of personal identities against government-issued identification through sophisticated facial recognition methods, liveness detection, and a comprehensive array of over 50 forensic and biometric tests, all executed within seconds, backed by the industry's most extensive document library. Additionally, FAD captures and records the precise moment a signatory provides their consent, ensuring complete accountability for the agreement. This innovative approach not only enhances the security of transactions but also builds trust in digital interactions.

The elsai Clinical Protocol Audit Agent assists clinical and regulatory teams in ensuring that protocols, consent documents, and recruitment materials are properly aligned with governance standards prior to IRB submission. This innovative tool offers artificial intelligence-driven validation across multiple documents, tracks amendments and versions, identifies discrepancies automatically, provides governance and audit traceability, and delivers IRB-prepared review summaries. Additionally, it seamlessly integrates with CTMS, eIRB, eTMF, as well as Word and Google Docs workflows, enhancing overall efficiency and compliance in the clinical trial process. Its comprehensive features make it an invaluable asset for teams aiming to streamline their regulatory submissions.

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.

Goodflag serves as a platform for electronic signatures and digital trust, tailored to assist organizations in signing, validating, and securing documents while adhering to rigorous legal and regulatory requirements, notably those outlined by the European eIDAS framework. This comprehensive solution caters to various digital signature needs, featuring simple, advanced, and qualified signature options, which empower users to select the right level of security based on the significance of each document. Additionally, Goodflag facilitates multi-party approvals, provides real-time updates on the signing process, and ensures secure storage, alongside offering electronic sealing to protect document authenticity and integrity against tampering. With the capability to integrate seamlessly with existing business systems through APIs and connectors, Goodflag allows organizations to embed signature workflows into their applications, thus streamlining and automating document management processes from start to finish. As a result, companies can enhance efficiency while maintaining compliance and security in their document handling practices.

Our offering transcends conventional digital signatures. By streamlining the document signing process, you can effortlessly enhance your business operations. ValidSign’s fully cloud-based service minimizes errors while bolstering your legal standing. Experience the simplicity of digital signing right away. The digital signature remains our reliable solution for executing essential documents, consistently receiving high marks for user-friendliness from both signers and stakeholders. ValidSign is versatile, accommodating the signing of contracts, quotations, purchase agreements, policies, and a variety of other documents. Additionally, the need for multiple signatories to gather at a specific place or time has become a thing of the past. With digital archiving, you can effortlessly maintain your contracts in an organized manner. ValidSign is widely adopted across numerous organizations in Europe and continues to expand its reach. With an extensive array of features, ValidSign stands out as a comprehensive enterprise solution for any business. It’s a platform equipped with a multitude of functionalities ready for your use, making it an invaluable tool for modern organizations.

ValidMind stands out as the premier solution for organizations seeking to streamline the automation of testing, documentation, and risk management concerning AI and statistical models. This comprehensive platform offers a range of tools designed to assist data scientists, corporations, and risk or compliance professionals in pinpointing and documenting potential risks linked to their AI models, ensuring adherence to regulatory standards. With its integrated features, ValidMind simplifies the review process of risk areas across various teams' models, allowing organizations to effectively prioritize compliance and risk mitigation efforts. Furthermore, ValidMind promotes collaboration by breaking down information silos, thereby alleviating the complexities involved in sharing and working together on model documentation, validation reports, and risk assessments throughout the entire model lifecycle. By leveraging ValidMind, organizations can foster a culture of transparency and accountability in their AI practices.

Introducing an eReg platform specifically tailored for study sites, it ensures rapid deployment without imposing rigid workflows, featuring a user-friendly design and functionality. Experience RegDoc eSafe free of charge today! This platform acts as a secure vault for source documents, equipped with tools that facilitate the transfer, redaction, and assignment of role-based, time-limited remote access to sensitive information. RegDoc eSafe boasts fast and flexible configuration options, requires minimal training for intuitive usage, and includes a comprehensive yet efficient validation process. The implementation is streamlined to quickly prepare your clinical study sites for operation. Additionally, regulatory binder templates are readily available within your site for convenient retrieval. The platform allows for user upload and access control settings, along with dedicated training sessions for both administrators and users. MedPoint prioritizes compliance, guiding you through all necessary procedures to validate our software effectively. With a wealth of experience in developing and supporting validated systems, MedPoint undergoes regular audits by study sponsors, ensuring the utmost reliability and quality in our offerings. Our commitment to continuous improvement and user satisfaction sets us apart in the industry.

Docuten serves as a comprehensive digitalization solution that aims to consolidate and automate various administrative functions, including digital signatures, electronic invoicing, and document management, all within one cohesive platform. This innovative tool empowers businesses to electronically send, sign, and certify documents with legal authenticity, adhering to all signature types specified by the eIDAS Regulation, while functioning as a Qualified Trust Service Provider to maintain compliance in over 90 countries. By streamlining document workflows, it minimizes manual interventions, speeds up signing processes, and enhances the experience for all stakeholders through secure, remote signing capabilities accessible from any device. Beyond just digital signatures, Docuten also transforms invoicing operations by enabling organizations to generate and receive electronic invoices in a centralized system, which boosts control, efficiency, and adherence to regulatory standards. Furthermore, this platform's integrated features not only facilitate seamless collaboration but also contribute to a more sustainable approach by reducing paper usage and minimizing environmental impact.

AassureComply is an international platform specializing in e-invoicing and finance compliance, designed to assist companies in navigating electronic invoicing, adhering to accounting regulations, managing tax controls, integrating with ERP systems, and streamlining regulatory workflows across various markets. This innovative platform empowers businesses to efficiently send, receive, validate, and monitor structured e-invoices while automating both invoice processing and compliance workflows, all while facilitating integration with current ERP and accounting systems via APIs, ensuring that financial records remain audit-ready. Additionally, AassureComply offers PEPPOL Access Point and SMP functionalities for secure electronic document exchanges, and it further supports finance departments with a range of features including invoice validation, tax and code mapping, management of multiple companies, role-based access control, comprehensive reporting, audit trails, payment tracking, bank reconciliation, management of purchase orders, goods received notes, inventory workflows, and user-friendly compliance dashboards, ultimately enhancing operational efficiency and regulatory adherence.

Docbyte operates as a European Trust Service Provider that focuses on solutions for digital archiving and document processing, aimed at ensuring both compliance and security while facilitating the long-term accessibility of digital records. The company's notable offering, the Docbyte Vault, delivers Qualified Electronic Archiving (QeA) services that align with global standards such as eIDAS 2.0, ISO 14721 (OAIS), and ETSI 119.511/512, ensuring that documents and digital signatures are meticulously preserved. Among its array of features, the Vault includes retention management, digital signature validation, evidence records, encryption, role-based access control, and capabilities for identifying and anonymizing personally identifiable information (PII). Furthermore, the Docbyte Vault is designed to integrate effortlessly with pre-existing IT systems and provides APIs that enable the validation and preservation of electronic signatures and documents, as well as the verification and creation of various documents. In addition to these core services, Docbyte also delivers solutions tailored for application retirement, secure document collection, and efficient digital mailroom management, further enhancing their comprehensive suite of offerings. Overall, Docbyte is committed to empowering organizations with reliable tools that safeguard their digital assets while ensuring adherence to regulatory requirements.

Digital Signature and Contract Management encompasses speed, security, and legal validity, offering a rapid method to securely produce documents, send them for signatures, and oversee contracts. With an emphasis on Digital Signature and streamlined Digital Contract Management, the process of creating and editing contracts has never been more straightforward! Within mere minutes, your contract can be finalized. Whether it's through digital, electronic, or hybrid signatures, these methods ensure both safety and legal recognition. Additionally, the management of contracts, deadlines, processes, and financial oversight allows for real-time tracking of your contract details, bringing everything into a singular, accessible platform. This is the most comprehensive solution available, facilitating everything from document creation to secure storage. You can monitor the status of all your digital contracts instantly, applying filters based on date, status, or subscriber. The capability to sign documents in bulk further enhances efficiency. Integration with the latest Pipedrive updates allows for seamless import of information from your Pipedrive leads into your documents on our platform, ensuring that once documents are signed, your leads are promptly updated, streamlining the entire process further. This convergence of technology not only simplifies contract management but also enhances productivity across the board.

sproof serves as a premier European platform dedicated to enhancing digital trust through signature and identity processes, specifically designed for organizations that demand the utmost in security, efficiency, and scalability. This comprehensive solution comprises six modular components, catering to all eIDAS-compliant signature levels, ranging from simple signatures to qualified electronic signatures (QES), while also offering integrated identity verification for smooth, legally compliant end-to-end operations. Central to the platform are two key features: sproof Sign, which facilitates electronic signatures across various levels (SES, AES, QES), and sproof Ident, which focuses on identity verification and qualified signatures. Enhancing its core capabilities are additional modules such as sproof Fastlane, which streamlines the process of acquiring legally valid e-signatures and collects form data with ease. Moreover, sproof Widget allows for the direct integration of eIDAS-compliant electronic signatures (FES, QES) into a variety of applications or websites. The platform also includes sproof Validate, an automation tool for the verification of digital signatures, and sproof eID-Hub, which establishes connections across Europe to facilitate seamless identity verification. By utilizing these versatile tools, organizations can ensure a robust framework for their digital transactions and identity management.

GoFirmex is a LegalTech firm that specializes in providing businesses in Latin America with secure electronic signature and digital document management services. The platform features Simple Electronic Signatures (SES), Advanced Electronic Signatures (AES/FEA), remote notarial authorization workflows, and API integrations, facilitating the digitization of contracts, onboarding procedures, HR tasks, financial agreements, and various legal documents. By utilizing GoFirmex, organizations can significantly lower operational expenses, speed up document processing, and enhance compliance with legally recognized digital signing methods that adhere to Chilean electronic signature laws. Its innovative technology caters to a wide range of sectors, including educational institutions, financial services, real estate firms, healthcare providers, and large enterprises that are pursuing secure and efficient digital transformation strategies. With the increasing demand for streamlined processes, GoFirmex continues to expand its offerings, ensuring companies can safely navigate the complexities of the digital landscape.

Vault QualityDocs enhances quality processes and mitigates compliance risks through automated workflows and thorough audit trails. By streamlining review and approval procedures, it ensures efficient sharing of SOPs and other GxP documents among staff and collaborators. The automation of workflows, coupled with real-time visibility into content status, empowers organizations to manage SOPs effectively, further minimizing compliance risks. Its user-friendly interface promotes higher adoption rates and operational efficiency. In addition, the system provides detailed audit trails, organized content, and robust search capabilities that greatly improve audit preparedness and inspections. Users can securely access and interact with documents via any major web browser, and if configured, can print, distribute, and monitor controlled PDF copies. The incorporation of predefined document taxonomies, metadata, and selection lists for quality, manufacturing, and validation documents not only streamlines operations but also enables organizations to swiftly embrace industry best practices, ensuring continuous improvement and compliance alignment. Thus, Vault QualityDocs stands as a pivotal tool in modern quality management.

An electronic signature that holds legal weight offers a secure, trustworthy, and convenient method for your business to send, approve, and sign digital documents. By streamlining your document processes, you can eliminate the need for paper entirely. Simply upload your PDF or .docx file and input the email addresses of the individuals who need to sign. Each signatory will receive a personalized link to provide their signature, ensuring a fully digital experience. This service can be accessed effortlessly from a computer, smartphone, or tablet, making it both user-friendly and efficient. Once the signing is complete, the document is safely encrypted within your account, allowing you to choose whether to save or export it as needed. There's no need for a digital certificate; just sign and proceed. This solution is suitable for various applications including commercial contracts, loan agreements, account openings, general documentation, insurance proposals, and school enrollments. Additionally, you can seamlessly integrate the electronic signature feature into your existing systems through Clicksign's REST API, which helps automate your signature workflows, enhancing productivity further. Embrace the future of document management and streamline your operations today.

KOŚA DMS is a comprehensive cloud document management solution tailored for organizations in the pharmaceutical, biotechnology, medical device, and broader life sciences sectors. It facilitates the creation, evaluation, authorization, distribution, and revision tracking of controlled documents, incorporating workflows for standard operating procedures (SOPs), policies, forms, and other essential quality records. With the ability to manage role-specific access, electronic signatures, audit trails, and periodic reviews, teams can ensure that document histories remain traceable for regulated processes. Integration with Microsoft Word enhances the drafting process, allowing users to work within a familiar authoring environment, while connections to ERP and LIMS systems enable seamless documentation linkage with operational workflows. Designed specifically for quality assurance, quality control, regulatory affairs, and document control teams, this system streamlines the coordination of document lifecycle activities across various sites and functions, ensuring compliance with industry regulations. Furthermore, the platform's user-friendly interface allows teams to efficiently navigate and manage their document processes without unnecessary complications.

Signatys provides a legally recognized electronic signature solution that is valid both in Switzerland and globally. You can securely gather signatures from customers and employees remotely, ensuring peace of mind throughout the process. Download documents and sign them digitally through our web desktop client or our specialized mobile app. Every action taken is logged and maintained in an audit trail, offering protection in case of disputes. We offer APIs for seamless integration into your existing systems and tools. Additionally, our eBanking integration allows documents to be signed directly from customer accounts. Transform any workflow that requires a signature into a digital process. Signatys excels in managing electronic signatures for documents that are sensitive and confidential in nature. Our solution can be implemented on-premises for enhanced security or utilized via our cloud service hosted in Switzerland, allowing you to choose the best option for your needs. Furthermore, our user-friendly interface ensures that both individuals and businesses can easily navigate the signing process.

Join countless businesses and professionals globally who rely on us as their premier source for secure digital signatures. Assure the veracity of your signers’ identities and the legal integrity of your electronic documents. Accelerate your document signing workflow by signing multiple documents simultaneously and streamlining the document preparation process for signatures. Remove the expenses associated with printing, handling, mailing, and storing paper documents for good. Confirm that you meet your legal requirements and adhere to industry standards. Transition to a paperless signing approach to lessen your organization’s ecological footprint. Step into the digital age with ConsignO Cloud, our electronic signature solution, which offers a free 30-day trial. Oversee your document signing process effectively while providing your clients, employees, and partners the convenience of signing documents anytime and from any location. By embracing this innovative platform, you can enhance efficiency and improve overall productivity in your operations.

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.

ENSUR is a document management and specification management software that automates the management and workflows of documents. This will help you streamline your business processes and improve your quality control. ENSUR is a secure repository that stores and organizes your business documents. It also includes tools for collaboration, version control and corrective and preventative actions, training, incidents, reporting, and many other features. ENSUR is available as a validated or non-validated solution. It helps you meet and exceed all regulatory compliance requirements such as FDA, ISO, GxP and OSHA. ENSUR can be installed on-premises behind your firewall, or in DocXellent Managed Cloud. It is highly secure and compliant with GxP compliance.

Sefin provides efficient, secure, and rapid solutions for electronic signatures and the digital oversight of various contracts. One of their key offerings, MMS Paperless, facilitates the integration of electronic contract signing within organizations. This solution ensures safety by allowing authorized personnel to access electronically signed contracts anytime and from anywhere, eliminating the risk of loss. It is designed for immediate use, characterized by user-friendly signing processes that enhance cost management and streamline the archiving of contractual documents. The Public Digital Identity System (SPID) simplifies the remote signing process, making it not only quicker but also more secure. When contracts are signed digitally using SPID, they attain legal validity and binding status across jurisdictions. Users can conveniently choose between a desktop version via a web browser or a tablet application for signing contracts, catering to diverse preferences and needs. This versatility enhances the overall user experience and promotes wider adoption of digital contract management solutions.

Digital evidence that is admissible in court includes qualified eIDAS timestamps and advanced electronic signatures, which hold legal validity throughout the European Union. This ensures that such evidence can be reliably used in legal proceedings across member states.

An automated tool designed for the analysis and validation of cloud platforms catering to regulated sectors is now available. With just a few minutes of setup, review, and approval, you can save weeks of tedious manual validation tasks. Validify takes care of the entire process for you. Within minutes, Validify produces all necessary documentation, thereby removing the need for lengthy scheduling and preparation efforts. The tool not only identifies but also confirms any changes made to your applications. While vendors may validate their standard releases, your tailored solution requires a different approach. By ensuring that your platform remains compliant, Validify provides peace of mind and efficiency in maintaining regulatory standards. Consequently, this solution enables organizations to focus more on innovation rather than on prolonged compliance processes.

Validation Manager is a cloud-based solution that streamlines the verification and validation processes for laboratory methods and instruments. Developed in collaboration with laboratories worldwide over the past decade, this software has demonstrated the potential to eliminate up to 95% of previously spent time on these tasks. More importantly, it fosters a shift in perspective and quality through innovative software solutions. The applications of Validation Manager extend from verifications and validations to routine quality control within labs. Additionally, test manufacturers can enable their clients to perform quicker verifications of their instruments and even carry out troubleshooting remotely. By centralizing quality data from multiple laboratories onto one platform, laboratory groups can fully reap the rewards of both centralization and standardization, enhancing their operational efficiency significantly. This integration not only improves workflow but also enhances the overall quality of laboratory outputs.

Evidency operates as a Qualified Trust Service Provider (QTSP), providing organizations with the tools to generate, oversee, maintain, and access legally valid digital evidence for their documents and data across their entire lifecycle. By integrating qualified timestamping, electronic sealing, and electronic archiving within one cohesive platform, Evidency guarantees the authenticity, integrity, traceability, and durable preservation of essential information. In addition to its comprehensive features, Evidency is built for effortless integration, allowing organizations to connect it to their current systems via a powerful REST API, which facilitates the automatic generation of trusted evidence, enhances compliance, and safeguards critical business information on a large scale. This flexibility and efficiency make Evidency a pivotal resource for modern enterprises navigating the complexities of data management and legal compliance.

AlphaTrust e-Sign™ enables the automation of both document and signature workflows, accommodating everything from straightforward present-and-sign scenarios to complex, multi-document, multi-party agreements that have different rules based on the participants involved. While electronic signatures are a remarkable feature, effective workflow automation requires more than merely affixing signatures to documents; it encompasses the entire process, including document creation, user authentication, data capture and validation, adherence to compliance regulations, signature acquisition, and the subsequent handling of documents and data post-signing. For organizations seeking to streamline the processes of document approval, signature collection, data gathering, and secure transmission, AlphaTrust e-Sign™ presents a superior solution. Moreover, AlphaTrust e-Sign™ serves as a comprehensive workflow automation hub tailored for both service providers and enterprise applications, facilitating the management of intricate use cases and handling high-volume transactions efficiently. This platform not only enhances productivity but also ensures that all elements of document management are seamlessly integrated.

Novatek International delivers extensive software solutions that not only fulfill but surpass the quality and compliance standards essential for the life sciences sector. Their process-specific offerings create an integrated platform that ensures uniformity and standardization across various departments within a single site and among multiple locations. This integration significantly lowers the total cost of ownership and enhances the return on investment. The NOVA-CPM tool is a cutting-edge automation solution that expertly manages all aspects of equipment qualification, calibration, and maintenance procedures. Designed with global regulatory compliance and data integrity in mind, the system features robust security protocols, electronic signatures, and comprehensive audit trails. As a premier Computerized Maintenance Management System (CMMS), NOVA-CPM encompasses the entire life cycle of equipment, addressing needs from initial purchase and validation to calibration, maintenance tasks, repairs, and ultimately, end-of-life replacement. This holistic approach ensures that organizations can maintain operational efficiency while adhering to stringent regulatory demands.

Qualitum is an innovative platform designed for computer system validation (CSV/CQV) specifically tailored for the regulated life sciences sector. It automatically generates IQ/OQ/PQ protocols, GAMP 5 classifications, and audit trails directly from primary documents such as URS, P&IDs, and SOP libraries, ensuring that each requirement is tracked comprehensively through a queryable graph that eliminates the need for traditional spreadsheet RTMs. The platform maintains strict adherence to ALCOA+ data integrity standards, monitoring every record instead of just samples, while allowing human reviewers to validate and approve the outputs produced by the agent. Qualitum operates on a single-tenant basis across AWS, Azure, or on-premises environments, empowering customers with control over their keys and prohibiting any training rights on customer data. It seamlessly integrates with existing systems of record, including Veeva, MasterControl, TrackWise, AVEVA PI, Tulip, and others, making it a versatile choice for organizations. Designed with the needs of Heads of Validation and validation consultancies in mind, it serves stakeholders in the pharmaceutical, biotechnology, and medical device industries. Interested parties can obtain a per-site annual license quote upon request, and a fixed-fee pilot program lasting 8-12 weeks is offered for a single system to facilitate an initial experience. This comprehensive approach ensures that organizations can achieve their validation goals efficiently while maintaining compliance in a highly regulated environment.

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

Scrive delivers a secure, scalable, and compliant eSignature and digital identity platform built entirely in Europe. It empowers organizations to automate document workflows, streamline customer onboarding, and ensure regulatory compliance across every transaction. As an EU Qualified Trust Service Provider (QTSP) under eIDAS, Scrive provides legally binding electronic signatures, advanced ID verification, and digital identity management—all backed by ISO 27001 certification and EU-based data hosting. Businesses can send and sign documents, build dynamic forms, and integrate Scrive directly into their CRMs or business systems via APIs. With ready-to-use templates and customizable workflows, companies can reduce manual handling by up to 80% while improving accuracy and customer experience. Scrive’s tools are tailored to regulated industries like banking, insurance, telecom, automotive, and real estate, where trust and compliance are non-negotiable. Its platform ensures auditability and data security for every transaction while centralizing control over digital documentation. Backed by 12,000+ satisfied clients and proven success stories from brands like Volkswagen, DNB, and Avanza, Scrive stands as Europe’s trusted choice for compliant digital transformation.

Veeam Recovery Orchestration & Compliance is a disaster recovery orchestration solution that helps organizations automate, test, validate, and document clean recovery. The product is designed to replace manual recovery steps with policy-driven workflows, repeatable runbooks, readiness checks, approvals, and automated evidence capture. It helps teams validate clean restore points in an isolated clean room before bringing workloads back into production. Clean Room Orchestration with YARA enables malware scanning and last-known-good restore point selection to reduce reinfection risk. Automated testing and disaster recovery drills help organizations validate RPO and RTO targets without disrupting production systems. Dynamic documentation generates recovery runbooks, timing records, approvals, outcomes, and audit evidence automatically. Veeam Recovery Orchestration & Compliance supports recovery on premises, to Microsoft Azure, and from repositories such as Veeam Data Cloud Vault and S3-compatible storage. Application-centric runbooks help model dependencies across databases, services, and virtual machines so systems recover in the right order. By combining orchestration, clean room recovery, malware validation, automated testing, compliance evidence, runbooks, and cloud recovery, Veeam helps organizations prove recovery readiness before disruption occurs.

Pathnovo is an advanced Intelligent Document Processing (IDP) solution that utilizes AI technology to streamline the extraction, classification, validation, and digitization of information found in intricate business documents. By integrating Optical Character Recognition (OCR), Computer Vision, Machine Learning, and Large Language Models (LLMs), the platform achieves a high level of precision when handling both structured and unstructured document types. It accommodates a variety of document formats, including invoices, Mill Test Certificates (MTCs), purchase orders, bills of lading, certificates, forms, and engineering documentation. Furthermore, Pathnovo provides customizable workflows, incorporates human-in-the-loop validation for quality assurance, maintains audit trails for compliance tracking, and supports API integrations with enterprise systems like ERP and CRM. This enables organizations to significantly minimize manual data entry tasks, boost operational efficiency, enhance the accuracy of their data, and expedite document-driven business operations on a large scale. As a result, businesses can focus more on strategic initiatives rather than getting bogged down by repetitive document processing tasks.

Experience the most secure and user-friendly method for digitally signing documents. Explore the diverse range of electronic signature options offered by VIDsigner, which is designed for both in-person and remote signing scenarios. By integrating advanced cryptography and biometrics, VIDsigner ensures a safe and legally binding way to electronically sign contracts and documents. This SaaS solution seamlessly connects via API Rest with a variety of software applications, including those used in healthcare, records management, and document management, in addition to HR, finance, sales, and logistics systems. VIDsigner provides a comprehensive suite of services that can be tailored to meet specific needs, whether signing multiple documents electronically with a certificate, using a tablet during client meetings, or signing from any location via phone, all while also offering reliable notification services to keep users informed. The flexibility of VIDsigner ensures that it can adapt to any signing situation, making it an invaluable tool for businesses across various industries.