Alternatives to ValGenesis
Compare ValGenesis alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to ValGenesis in 2026. Compare features, ratings, user reviews, pricing, and more from ValGenesis competitors and alternatives in order to make an informed decision for your business.
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1
Qualio
Qualio
Qualio is the leading quality and compliance platform built exclusively for emerging life sciences companies. MedTech, pharma, biotech, and diagnostics teams use Qualio to standardize quality processes, connect them to regulatory obligations, and gain real-time visibility into compliance health. With a modern eQMS at the core and Compliance Intelligence layered on top, Qualio helps teams get audit ready in weeks and stay audit ready forever — without spreadsheets, fire drills, or heavyweight GRC systems. What Qualio delivers: ✔️ Audit ready in weeks ✔️ Inspection ready anytime — no fire drills ✔️ Faster market entry ✔️ Lower total cost of compliance ✔️ Confident, risk-managed scaling -
2
LabWare LIMS
LabWare
14,000 laboratories. 125 countries. 98% customer satisfaction! Improve your lab's productivity, throughput, efficiency, data integrity, and compliance with LabWare's suite of laboratory automation solutions. LabWare offers flexible deployment options. Laboratories who are eager to deploy within 30 days can choose the cost-optimized + fully validated SaaS LIMS that contains best practice workflows. Laboratories that need a fully customizable enterprise-level LIMS/ELN can choose between flexible cloud or self-hosted deployment options. LabWare users enjoy world class features such as: lot management, sample management, stability management, environmental monitoring, instrument interfacing, workflows and dashboards, inventory management, COAs, barcoding, and much more! -
3
Lockbox LIMS
Third Wave Analytics
A sample tracking, test result capture, and inventory management cloud LIMS for life science research, biotech/NGS, and industrial QC labs. Includes regulatory support for CLIA, HIPAA, Part 11, and ISO 17025. Nothing is more critical to a lab’s success than the quality, security, and traceability of samples. The Lockbox LIMS system provides robust sample management functionality to laboratory professionals, giving them full visibility on every aspect of a sample’s journey, from accessioning to long-term storage. LIMS analysis is about more than just tracking results- Lockbox’s multi-layered sample storage and location management functionality allows you to define your lab’s storage framework using a variety of location options: rooms, storage units, shelves, racks, boxes, and positions. -
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Total Lean Management (TLM) Software
Lean & Mean Business Systems
Perfect for a small company, TLM has everything you need, and can accelerate the implementation with consulting, training, procedure templates, and document writing/coaching support, plus we have validation templates and a system setting mode so small medical device companies have special features to help manage technical files and 510K submittals. TLM QMS Software saves you money AND makes your QMS more effective by providing a dual technology landscape for the two distinct QMS user types. Core modules include: • Audits • Contact Manager (CRM) • CAPA • Customer Feedback • Document Management • Electronic Forms • Employees • Employee Feedback • Equipment Calibration • Evaluations • FMEA • Inspections • Inventory/parts • Library • Meetings/Reviews • Metrics • Projects • Purchase Orders • Quality Record Mgt • Rejected Materials • Risk & Opportunities • Sales Orders • Strategic Planning • Surveys • Tasks/Events • Training • Work OrdersStarting Price: $45/user/month -
5
Dot Compliance QMS
QMS for Life Sciences
Dot Compliance provides the industry’s first off-the-shelf QMS solution – ready to deploy from day one, with little to no setup required, while also incorporating industry best practices and standards that address the latest global regulatory requirements. Powered by the Salesforce.com platform, our solutions enable life science organizations to quickly digitize their quality and compliance processes including Document Management, Training Management, Change Control, CAPA, Customer Complaints. Compliant with 21 CFR part 11, EU-Annex 11 and support ISO 9001, 13485, 14971, 27001 & MORE! Processes included: ▶ Document Management ▶ Training Management ▶ Quality Event Management ▶ CAPA Management ▶ Change Management ▶ Complaint Management ▶ Audit Management ▶ Supplier Quality Management ▶ Risk Management ▶ Design Control ▶ Deviations/Non-conformances ✔ Seamless Install ✔ Cost Effective ✔ One-Stop-ShopStarting Price: $10,000 / Annually -
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SimplerQMS
SimplerQMS
SimplerQMS offers a cloud-based Quality Management Software that is fully validated according to GAMP5 and specifically designed for the Life Science industry. This comprehensive QMS platform helps ensure compliance with various regulatory requirements, including FDA 21 CFR Part 11, EU Annex 11, GxP, cGMP, GAMP 5, GDPR, EU IVDR & EU MDR, ISO 13485:2016, 21 CFR Part 820, ICH Q10, and others. The software offers a wide range of Life Science QMS modules, such as Document Control, Change Management, Training Management, Supplier Management, Complaints Management, Non-Conformance and Deviation Management, CAPA Management, Audit Management, Technical Documentation Management, Risk Management, Quality KPIs, among others, ensuring a seamless experience. SimplerQMS enhances document handling by allowing users to work directly in Microsoft Office applications like Word, PowerPoint, and Excel.Starting Price: $13,750/year -
7
QT9 QMS
QT9 Software
Struggling with complex compliance requirements or disconnected quality systems? QT9 QMS eliminates these challenges with one integrated, fully validated platform that scales with your business. Designed for life sciences, aerospace, and manufacturing, QT9 offers cloud or secure on-premise deployment to meet your needs. Stay audit-ready automatically with built-in FDA, ISO, and EU MDR compliance while reducing manual work by up to 70%. With 28+ modules included—like document control, CAPA, training, and supplier management—QT9 deploys fast without costly customization. Backed by ISO 27001 certification, unlimited support, and 20+ years of proven success, QT9 helps 1,100+ organizations accelerate compliance, improve visibility, and simplify quality management. Start your free trial or book a personalized demo today.Starting Price: $10,000/year -
8
Avalon Laboratory System
Computer Service & Support
Sophisticated and HIPAA-compliant, the Avalon Laboratory System is specifically designed to manage the production and billing needs of clinical, esoteric, and toxicology laboratories. Developed by Computer Service & Support(CSS), this modular laboratory information system offers an array of features for reference laboratory automation. The solution also provides a rich set of modules for microbiology, pain management and toxicology, rescheduling, remote laboratory, SQL Access, electronic medical records, pharmacogenomics, and more. In addition, there is Avalon BI (Business Intelligence) for billing. With Avalon LIS and Avalon BI running on the same platform, there is a reduction in errors and duplicate entry of data. The billing portion also offers up-front eligibility and diagnosis validity checking. In Avalon BI, there are even more robust reports for revenue cycle management. -
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Intellect
Intellect
Intellect QMS is the latest version of Intellect's flagship product designed to help organizations and quality leaders meet FDA, ISO, and other global GxP regulatory compliance requirements. Intellect offers faster implementation time, robust out-of-the-box QMS capabilities, and extreme configurability to modify or build new apps. Empower your onsite and remote workforce with virtual auditing, online approvals, 21 CFR Part 11 electronic signatures, and ensure your team can access only approved and up-to-date quality documents, data, reports and analytics anytime, on any device. Intellect’s Environmental, health, safety and quality (EHSQ) software acts as a data management system for capturing, storing, and analyzing information related to occupational health and safety, waste management, and sustainability. It aims at reducing operational risk and improving health while attaining sustainability goals. -
10
Teamcenter
Siemens
Teamcenter® software is a modern, adaptable product lifecycle management (PLM) system that connects people and processes, across functional silos, with a digital thread for innovation. The unmatched breadth and depth of the Teamcenter portfolio mean that you can solve more of the tough challenges required to develop highly successful products. From the easy, intuitive Teamcenter user interface, people across the organization can take part in the product development process more easily than ever before. No matter how you choose to deploy Teamcenter – whether it be on-premises, on-cloud, or SaaS delivered via Teamcenter X – you get the same proven solutions designed to help you innovate faster. Get started with Teamcenter by taking control of product data and processes, including 3D designs, electronics, embedded software, documentation, and your bill of materials (BOM). Reach greater returns on your PLM system by leveraging your product information across more domains and departments. -
11
Validfor
Validfor
Validfor is a secure, modular digital validation platform that centralizes the entire validation lifecycle on a single, paperless system. Designed specifically for regulated industries, Validfor enables efficient validation while ensuring full compliance with GAMP 5, 21 CFR Part 11, and EU Annex 11. The platform supports electronic records and advanced electronic signatures with full audit trails, role-based workflows (Author, Reviewer, Approver), and complete CSV compliance. All documents and records are securely managed in a centralized repository, capturing every change with full traceability to protect data integrity and Quality Assurance. Validfor offers integrated modules for Change Management, Deviations, Testing, and Periodic Reviews, enabling seamless impact assessments, CAPA tracking, Computer Software Assurance (CSA), and audit-ready lifecycle management. -
12
DHC VISION
DHC Business Solutions
We offer solutions for companies with a high demand for quality. Our software solutions inspire with a modern UX, useful functionality, high modularity, and consistent compliance. Integrated solutions for quality management and quality assurance. Focused on the digitization of controlled documents and QA processes. Solutions specifically designed to meet the needs of the financial industry for the written rules of procedure, management of policies, and the control of information security. The cloud-based, pre-validated solution to automate your validation processes and to digitally control and manage validation documents. Early set-up of a digital QMS with a dedicated solution for startups and young companies. Based on DHC VISION. It can be used out of the box with immediate compliance and no license costs. Together, we digitize quality management and quality assurance processes and ensure regulatory compliance. -
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Veeva Vault QualityDocs
Veeva Systems
Providing automated workflows and comprehensive audit trails, Vault QualityDocs reduces compliance risk and improves quality processes. It accelerates review and approval processes and facilitates the sharing of SOPs and other GxP documents among employees and partners. Automated workflows and visibility into the content status and processes enable effective SOP management, reducing compliance risk. Intuitive, easy-to-use user interface drives adoption and efficiency. Detailed audit trails, content organization, and powerful search facilitate better audits and inspections. Securely access and use documents from any major web browser, or if enabled, print, distribute, and track controlled PDF copies. Predefined document taxonomy, metadata, and pick lists for quality, manufacturing, and validation documents facilitate operational harmonization and allow organizations to quickly adopt best practices. -
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Scilife
Scilife
Revolutionize your Life Sciences processes. Drastically improve the control, efficiency, and quality of your processes and products. Ensure inspection readiness at all times through our fully compliant platform, pre-validated according to GAMP5. Maintain total control over processes and documents, customize workflows to perfection, and automate where possible. Enjoy uninterrupted workflows and full traceability through seamlessly connected and integrated modules. Our dedicated team is ready to answer your questions at any time. Only a first-class Scilife experience will do! Our Scilife platform streamlines automates and organizes every process in your industry space, whether you’re in Medical Devices, Pharma & Biotech, or ATMP. Click below to discover which Scilife modules support your unique industry lifecycle stages. Our software is equipped with all the advanced quality tools you would expect, and a bunch more that go above and beyond!Starting Price: $1000 -
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Validation Manager
Finbiosoft
Validation Manager is a cloud-based software service that automates the verifications and validations of laboratory methods and instruments. It has been developed for over a decade together with laboratories around the world. Our customers have measured that even 95 % of the time previously wasted can be removed with Validation Manager. What is most important, however, is the leap in quality that can be reached with a new mindset and new software solutions. Validation Manager use cases range from verifications and validations to routine quality control of the laboratory. Furthermore, test manufacturers can empower their customers to conduct faster verifications of their instruments, and even conduct troubleshooting activities remotely. Laboratory groups can achieve full benefits of centralization and standardization by collecting quality data from all laboratories into one centralized platform. -
16
TheraBill
TheraBill
Therabill is a cloud-based practice management software for nutritional, mental and behavioral health specialists. Therabill combines therapy billing, scheduling, and documentation in one simple solution, allowing users to submit claims, manage schedules, enter treatment notes, and maintain patient information with ease. Therabill also offers a chock-full of helpful features including exportable client statements and invoices, automated appointments and reminders, and provider portals. -
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Carizma QM
Axicos
Carizma QM is a web-based software that supports users in managing the entire lifecycle of regulated documents from authoring, review, approval and release to archiving. Creation and management of regulated documents, e.g. SOPs. Integrated workflows for review and approval. Automatic start of training workflow, read and understood upon approval. Electronic signature – 21 CRF part 11 compliant. Display of users who have read and understood. Validated and audit trail. Supports users to manage the entire lifecycle of regulated documents within Carizma-QM itself. The author defines key information e.g. document type (SOP, work instruction, form, checklist, etc.), title of document, process owner (department), groups of users to whom the document is applicable, review cycle. Users are defined in due time by e-mail when a document needs to be reviewed. Carizma creates the skeleton document. -
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Virje
Virje
Virje complies with the requirements of 21 CFR Part 11, 21 CFR Part 820, and ISO 13485. Overwhelmed by the thought of Part 11 software validation? Accessible from wherever you are, for whenever you work. Eliminate paper, reduce cost, and increase efficiency with automation and centralized collaboration. Perfect for small to medium-sized businesses. Built from the ground up specifically for medical device quality management. A system that is flexible enough to adjust to your workflows and processes, without having to compromise. Configurable change order approvals by employee role and by document type. Notifications to responsible personnel at every stage in the change process. Ability to designate material dispositions for individual documents. Easy access to released and historical versions of documents. Quick viewing of document change history. Tracking of where-used locations and distributed hard copies. Periodic document review notification. -
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InSilicoTrials
InSilicoTrials
InSilicoTrials.com is a web-based platform, which provides a user-friendly computational modeling and simulation environment where many integrated easy-to-use in silico tools are readily available. The platform targets primarily users from the medical devices and pharmaceutical sectors. The in silico tools available for medical devices enable computational testing in different biomedical areas like radiology, orthopedics and cardiovascular during product design, development and validation processes. For the pharmaceutical sector, the platform provides access to in silico tools developed at all stages of the drug discovery and development processes and for many different therapeutic areas. We have built the only cloud-platform based on the crowdscience concept that makes it easy to use validated models and cut your R&D costs now. A growing catalogue of models ready to be used, on a pay per use basis. -
20
TestStream
Vedant Health
TestStream is not a test tool. However, through intelligence, it provides automated large-scale and thorough attention to detail in validating clinical systems… automated testing without the need for test scripts. In addition to offering extensive testing capabilities, TestStream provides complete quality and safety assurance for your clinical systems. By identifying build and maintenance issues, validating processes, finding the root causes of problems and more, TestStream helps ensure that all the pieces in your systems are connected, running smoothly and working the way they should—so your patients get the safest and best care. -
21
QUMAS EQMS
Dassault Systemes
To bring new products to market as quickly as possible in compliance with global regulations, organizations need to standardize and automate their business processes that manage the collection, tracking and analysis of information and the resolution of related issues. QUMAS EQMS (formerly ProcessCompliance) is a cloud-based solution for Enterprise Quality and Process Management that delivers comprehensive integrated regulatory, quality and compliance management capabilities in a validated QMS environment. QUMAS’s data-centric approach allows you to flexibly manage quality content and to access and re-use all quality data, providing comprehensive visibility into Quality. QUMAS’s interactive quality dashboards provide QMS overview across business areas and quality initiatives. Reports are available for export, email and scheduling. QUMAS allows QMS departments to exchange information securely, efficiently and compliantly in the cloud. -
22
ACE Essentials
PSC Software
Reduce risk with ACE Essentials, the pre-validated Electronic Quality Management System (EQMS) software created for all highly regulated industries. ACE Essentials comes equipped with 10 workflows built in and all the necessary Standard Operating Procedures and Policies, resulting in a fully compliant quality management system from the beginning. Understand the risks associated with your assets with ACE Essentials features including a full audit trail tracking every single action in the system. Pre-Configured Workflows. Pre-Configured Event Management (Due Dates, Scheduling and Reminders). Pre-Configured Permission-Based Security. Full Documentation Pre-Configured. 50+ Documents. Multiple Site Capability. Free Upgrades Throughout the Life of the Product. Pre-Configured Tasks List. No Validation Time. Pre-Configured In-System Notifications. Pre-Configured Email NotificationsStarting Price: $500 one-time payment -
23
Lab Online
Analis
Lab Online is a next-generation open web based* platform designed by Moonchase with state-of-the-art technology. Developed "from scratch" by a Belgian team of engineers active in this field for more than 20 years, this LIS platform supports all of the prescription, execution and reporting processes for clinical biology analyzes. Lab Online includes more than 70 different modules offering for all actors in the clinical biology laboratory (internal and external) lab functionalities such as: instrument communication, automated result validation, quality control, on line consultation of results in real time and even more so. -
24
QM
SOLABS
Document control made simple, document lifecycles, create, review/approve, revise, and retire documents. All transactions are recorded with e-signatures and timestamps and stored in the Audit Trail. Audits from start to finish. From audit planning to audit preparation and all the way to audit closure, track and document your internal and external audits with the SOLABS QM10 Audit APP. Intuitive reporting because trending and tracking are so critical to any quality management system, the SOLABS QM Essentials package includes advanced reporting capabilities. The reports and dashboards are available in formats that are easy to use, customizable and share the most common formats, whether it be Excel, PowerPoint, PDF, etc. with anyone within your organization. Create, assign, schedule and monitor training in a few clicks. Leverage online assessments to validate your team’s learnings. The SOLABS QM Training section allows you to handle all aspects of training. -
25
Laby
Laby
Experiment with new methods for managing your projects and data. Small, medium, or large structures, Laby adapts perfectly to your organization and your areas of expertise. Join our community of users and let’s develop tomorrow’s innovations together. Organize your projects, experimental plans, and essays. Develop a recipe for the manufacturing of finished products. Automate item management and traceability. Supervise laboratory instruments and manage their maintenance. Laby allows the centralization of all your files on a single platform for easy access and retrieval. Prepare and validate quality documents before distribution. Search, share, and consult all scientific papers. Sign reports based on 21 CFR part 11 and EIDAS standards. Track time spent by project, and export data. Complete management system allowing a high standard of monitoring. Receive training in order to get to work quickly and save time every day.Starting Price: €69 per month -
26
Qualis LIMS
Agaram Technologies
Qualis LIMS is an enterprise-class laboratory information management system used in industrial, analytical, & commercial sample testing across several industry verticals such as pharmaceutical, life-sciences, contract research, clinical research etc. Qualis LIMS has built-in integrated modules to manage all laboratory processes & help labs perform their tasks in an automated and paperless manner while enabling them to fulfil regulatory compliance requirements & adhere to industry standards. It digitally transforms labs by helping them: • In managing, storing, & aliquoting of samples. • Record final results of tests & experiments - manage tests, projects, samples, instruments & inventory in one central secure database. • Meet data integrity & regulatory compliance requirements such as GxP, ISO17025, 21 CFR Part 11 & EudraLex Annex 11 without any compromises. -
27
Waaila
Cross Masters
Waaila is a comprehensive application for automatic data quality monitoring, supported by a global community of hundreds of analysts, and helps to prevent disastrous scenarios caused by poor data quality and measurement. Validate your data and take control of your analytics and measuring. They need to be precise in order to utilize their full potential therefore it requires validation and monitoring. The quality of the data is key for serving its true purpose and leveraging it for business growth. The higher quality, the more efficient the marketing strategy. Rely on the quality and accuracy of your data and make confident data-driven decisions to achieve the best results. Save time, and energy, and attain better results with automated validation. Fast attack discovery prevents huge impacts and opens new opportunities. Easy navigation and application management contribute to fast data validation and effective processes, leading to quickly discovering and solving the issue.Starting Price: $19.99 per month -
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1factory Manufacturing Quality
1factory
1factory's Manufacturing Quality is a cloud-based and on-premises quality control software solution specifically created for manufacturing companies of all types and sizes. Powerful, reliable, and secure Manufacturing Quality by 1factory provides first article inspections, factory monitoring, quality control plans, in-process and final inspections, incoming inspections, inspection management, CAPAs, non-conformances, and more. Additional key features include running metrics calculations for Process Performance (Pp, Ppk), Process Capability (Cp, Cpk), variation / SPC control management, defect-risk monitoring, and more. -
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BioRAFT
RAFT
Our team of scientists and EHS professionals have years of experience working in laboratory safety and risk management to solve critical challenges. At BioRAFT, we understand the need for a software platform that simplifies safety tasks allowing scientists to get back to their research. Functionality can be added as your organization’s needs evolve through the addition of modules. BioRAFT works collaboratively with customers to develop new functionality. Reduce total operational costs with a single, easy-to-use system that improves laboratory safety and increases efficiency. Manage chemical inventory with a robust chemical database. Easily generate complex regulatory reports. Assign, conduct, and review inspections and self-inspections based on hazard and risk criteria, which drives real-time data analysis dashboards. Offer a comprehensive health and safety training program with user-specific assignments, automated requirements, and reminders. -
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FORM OpX
FORM.com
Compliance software that drives operations. Improve safety and increase accuracy with the top mobile audit and inspection platform for teams trusted by Walmart, Wendy’s, and Fannie Mae. Upgrade your paper, Excel, and digital processes to the #1 field management platform for teams. FORM OpX combines advanced data collection and configurable workflows with powerful operational insights to boost compliance in real-time. Configure audits, inspections, and workflows to ensure teams consistently follow procedures and meet regulatory obligations. Capture data instantly with digital forms that guide teams to the right action. Configure automated alerts and escalations to trigger corrective action as soon as issues arise. Save time and money with customizable workflows that improve processes and increase compliance — everywhere. -
31
eQMS::LIMS
Pardus
The application of this LIMS system establishes full control over the procedures of safety and quality control of products, raw materials, procurement procedures, production processes and environmental indicators. eQMS :: LIMS enables the establishment and implementation of demonstrable traceability, thus ensuring the maintenance of compliance with legal regulations and adopted standards, and thus significantly facilitates the implementation and day-to-day implementation of regulatory requirements. This modern LIMS system extends its functionality beyond the laboratory, especially in the field of quality management, enabling systematic monitoring and supervision of all resources and audit of all business units.Starting Price: $5000.00/one-time -
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SoftExpert EQM
SoftExpert
SoftExpert EQM is the most comprehensive enterprise quality management software (EQMS). It helps companies to achieve and maintain ISO 9001 certification through automated, highly interactive quality processes tailored to an organization’s specific products, operations and business practices. As a modular and scalable solution platform, SoftExpert Quality Management Software seamlessly integrates all key quality initiatives, including process mapping, documented information (SOP – standard operating procedures, work instructions and records), non-conformance reports (NCR/NCMR), corrective/preventive actions (CAPA), quality indicators (KPIs). The solution also manages supplier relations, customer complaints, quality audits, competence and training, quality risks and controls, quality inspection and statistical process control, increasing QMS agility and robustness. -
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Ennov Process
Ennov
The Ennov platform includes its own workflow engine that provides advanced capabilities. Workflows are used in Ennov Training, Ennov eTMF and Ennov RIM. They allow control of the sequencing of tasks and data modification while providing visibility across the organization. Workflows are entirely configurable by functional administrators (through a graphical interface). Coherence checks are performed whenever you save modifications in order to make sure they do not cause inconsistencies. Thus, Ennov guarantees workflows are coherent and reliable. Each Ennov workflow is associated with a configurable form. Data entry is facilitated using dynamic sections that are displayed – or not – depending on previously entered field values (for example: the type of Incident). The connected user enters free text, selects values in picklists and adds additional files when needed. An electronic signature can also be required to complete a workflow step. -
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Autoscribe Matrix Gemini LIMS
Autoscribe LIMS
Laboratories need to accurately manage large volumes of data to strict standards, while at the same time constantly evolve to improve efficiency, automation and turn-around times. Autoscribe Informatics' Matrix Gemini LIMS (Laboratory Information Management System) is designed to be flexible enough to meet these exacting needs. There has always been a trade-off in choosing a LIMS - configurability vs. custom coding. Autoscribe Informatics solutions uniquely feature genuine configuration capabilities, with no custom coding, to ensure an exact fit to customer requirements for a wide range of laboratories and processes. Matrix Configuration Tools provide superior flexibility which results in fast implementation and an interface that is familiar and comfortable for each user. In addition, a product that is easy to configure results in a long system life and therefore a reduced cost of ownership. -
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3rdwave
3rdwave
We have solved 3 intractable supply chain challenges to enable you to experience the pinnacle of visibility. Capturing and validating supply chain data, weaving it together to get a holistic view of your supply chain, and translating that holistic view into different perspectives required by internal functional stakeholders to make informed decisions. Welcome to the new world of automation. With supply chain data validated and understood, organizations are now able to automate across functional silos like never before. It is time to start using your employees to make high valued decisions and start the process of eliminating spreadsheets and manual entry. Unleash the power of having all of your supply chain data centralized, validated, and controlled. Decisions can be made with certainty and executed faster; problems can be identified and rectified with greater speed. Your organization will have the agility to organize and reorganize like no other.Starting Price: $1995.00/month -
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Penneo
Penneo A/S
Penneo is a digital signature and digital transaction management software that helps companies in multiple industries and departments digitize and automate their document-based processes. Our digital signatures meet the eIDAS requirements for advanced electronic signatures. Therefore, they are just as legally binding and valid as handwritten signatures. Penneo is particularly suitable for companies in heavily regulated industries due to its compliance with the GDPR, eIDAS, and Anti-Money Laundering regulations. By using Penneo, businesses can easily meet their regulatory compliance obligations.Starting Price: €129 / month -
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CASQ-it
BÖHME & WEIHS
Defect-free business processes lead to defect-free products. And that is exactly why CASQ-it is designed to encompass all the steps in your quality assurance and quality management processes – starting with the development process, continuing through the material process – up to and including your support processes. The advantage of CASQ-it lies right here in this process-oriented mode of operation – functionality that enables your CAQ system to adapt flexibly to your processes – and not vice versa. CASQ-it supports your quality assurance processes on their journey into the future: Quality and reliability increase customer satisfaction whilst reducing the cost of quality. Each separate CASQ-it module functions independently – enabling you to optimize individual processes and workflows within your company right from day one. Our modules can be flexibly combined – or used to create a comprehensive quality assurance system. -
38
Zuken GENESYS
Zuken
GENESYS is Zuken's model-based systems engineering platform designed to manage and communicate product information effectively, enabling teams to focus on innovation. It supports the entire engineering process from initial concept to verification and validation within a single environment, capturing all relevant product information across different levels, from high-level use cases and system context to system and subsystem definitions, down to detailed design connections. GENESYS ensures every system design is coherent, consistent, and complete, providing feature-rich authoring capabilities with automatic diagram generation and rule-based formatting. It offers validation of logical consistency and behavior enabled by executable models and seamless integration with existing authoring tools. Built upon the Comprehensive Systems Definition Language (CSDL), which conforms to the Systems Modeling Language (SysML) standard, GENESYS provides semantic precision. -
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Nova-QMS
Novatek International
Maintaining consistent product quality and quality processes can be challenging in today’s pharmaceutical manufacturing environments. Regulated industries such as the Pharmaceutical, Biotech and Life Sciences are required to maintain Good Manufacturing Practices (GMP) to meet regulatory requirements. Not only do you need to meet GMP requirements you must also be able to prove this. Using paper-based forms, disconnected systems, or manual processes to manage, track and report on quality issues and actions does not provide effective solutions for implementing harmonized, integrated quality management processes, which follow industry best practices. -
40
LabSpeed
Topos Technologies
LabSpeed™ Results Analysis software provides a common platform for charting, reporting, exporting, monitoring, validating, sharing, and analyzing results generated from all types of instruments used in a laboratory, from hand-held devices to multi-element analysis spectrometers and bio-tech instruments. Gain instant access to your instrument data with little or no setup. LabSpeed handles data formats and connections automatically. An intuitive drag & drop interface makes it easy to quickly build the solutions a laboratory needs to use on a daily basis to become more productive. LabSpeed works simultaneously with data from all types of analytical instruments regardless of type or complexity. Run LabSpeed at the instrument for data review, exporting and printing, or in the office for research, data analysis and advanced publishing. LabSpeed includes advanced capabilities and features normally found only in separate software packages such as Crystal Reports®, SigmaPlot® and InfinityQS®.Starting Price: $695 one-time payment -
41
Labsoftware
Labsoftware
Labsoftware.pk is a cloud-based Laboratory Information Management System (LIMS) designed to streamline diagnostic lab operations with a user-friendly interface. The platform seamlessly integrates core lab functions, including patient registration, sample collection, automated billing, report generation, and management of lab databases, enabling smooth coordination across administrative, operational, and patient-facing activities. Its SaaS delivery ensures accessibility and scalability, empowering laboratories to digitize workflows, reduce manual errors, and enhance operational efficiency. With comprehensive features like instant sampling workflows, centralized patient history, billing automation, and real-time reporting, all within a modern, browser-based system, Labsoftware.pk serves as a holistic, cloud-native solution tailored for diagnostic labs. -
42
AssurX
AssurX
The AssurX platform is a versatile enterprise quality management system (EQMS) and regulatory compliance management platform. AssurX allows enterprises of any size or complexity to create a system that reliably communicates and coordinates quality and compliance information, documentation, and activities across the enterprise. AssurX allows regulated businesses to quickly identify and control risk exposure and avoid quality or noncompliance problems while improving workflow. AssurX QMS software is highly configurable to fit any established or dynamic business requirements. The system creates an electronic workflow of tasks, alerts, escalations, and approvals that can be automated to the desired level, mapping precisely to real-world operations. Begin with just the solutions and functionality you need now, then implement what you like whenever you’re ready. No other system is easier to deploy, configure, and modify. -
43
AmpleLogic Quality Management
AmpleLogic
AmpleLogic's Quality Management Software (eQMS) is intricately crafted to meet the rigorous requirements of heavily regulated industries. The ISO 9001 certified cloud-based Quality Management System (QMS) is ideal for Lifesciences, Food & Beverages (F&B), Cosmetics, Medical Devices, Gene Therapy, and analogous sectors. As businesses acknowledge the challenges associated with manual quality checks—prone to both laborious efforts and errors—they are increasingly adopting QMS software solutions. These systems play a pivotal role in enhancing audit quality through process automation, efficient data management, and seamless API integration. -
44
RQM+
RQM+
RQM+ is a global medical technology service provider focused on accelerating compliance and market success. Through our unparalleled expertise and industry knowledge, we deliver specialized solutions and expedite the journey along the full product lifecycle for medical technology companies, from concept to commercialization to post-market. Our portfolio of services enables the delivery of end-to-end solutions across the complete medical device product lifecycle. RQM+’s quality assurance engineers review material lists, set up suppliers, and support the design change process. RQM+’s design quality engineers help support packaging, sterility, biocompatibility, and device testing that may be needed. RQM+’s regulatory affairs consultants provide guidance and help with submissions to the FDA, notified bodies, or other government agencies. We use our extensive experience with the latest reimbursement requirements and value-based compensation models. -
45
Dragonfly PHD
Dragonfly PHD
Online appointment scheduling and registration to collect everything you need in advance. Email, text and chat to reach patients with reminders and care follow-up. Automated reporting for insurance claims and regulatory compliance. Best in class privacy and security standards. Manage vaccines and testing at scale, including scheduling, intake, reporting, and follow-up. Accessible via phone/tablet, no app needed. Paperless lab integration to deliver results immediately. Patients receive confirmations via text and email. Flexible scheduling tool for website events & employer dashboard. State reporting, registry integration, and exports for claims processing. Built on proven enterprise software platform managing millions of transactions. Customizable templates to promote your service.Starting Price: 5% fee per procedure -
46
Infosequre Security Awareness
Infosequre
Our immersive security awareness e-learning modules are the main tool in building a strong and lasting security culture. Chock-full of easily absorbed information and developed using the best awareness techniques, they make your employees aware, alert and informed. Our highly customizable phishing simulation can be added to your program for complete training, or used on its own as a way to test and train your team in real-time. Take your security awareness training to the next level with our game-based learning experiences specifically designed to complement e-learning and cement security awareness in the minds and behavior of your people. Play our VR game or escape our truck before the bang. A real custom security awareness program is based on precise measurements that give you the edge you need. Stay in the loop and gain powerful insights into your company's progress. -
47
Almond
Almond
Almond is a professional, cloud-based, quality management software for healthcare companies. The software enables computerized management of the quality processes in compliance with regulatory requirements. The system maintains a document audit trail, and full document indexing and ultimately achieves documented evidence of all QMS processes. Manage your suppliers seamlessly through the electronic organization of certificates and agreements; all information is concentrated in one place. Assign permission to your suppliers to perform training, required by your system at their premises, using your quality system. Receive automatic email notifications before supplier certification expires. An electronic control dashboard allows you to be updated at any time on the status of the project. Create as many logbooks as you need, with no budget considerations or storage restrictions. Automatic conversion to effective after training completion. -
48
SOFTDMS
Pharma Soft Sol
Pharmaceutical and Biotech companies are challenged to meet control documentation requirements in day-to-day operations. Effective document management and document control are critical parts to any quality and compliance solution. Global Regulatory agencies expect that all regulated companies follow current industry best practices throughout the manufacturing process. To meet these requirements Phama Soft Sol developed Document Management System software which helps to control and distribute the SOP’s , STP’s and other regulated documents. Document management software systems not only reduce the costs of compliance but also help you improve process and product quality. Document Management System(softDMS) able to retrieve the information you need exactly when you need it-minimizes the possibility of miscommunication and mistakes which in turn minimize risks, manhours and other documentation errors. -
49
DELMIAworks
Dassault Systemes
Combine manufacturing, MES, supply chain, and ERP software to optimize your shop floor. Learn how DELMIAworks (formerly IQMS) can help increase visibility into every aspect of your manufacturing operation and solve your most trying production challenges. Prevent unnecessary downtime, while increasing manufacturing efficiency, quality, and profit margins. Improve decision making with real-time access to data across the entire supply chain. A single system for all ERP, manufacturing, MES, and supply chain requirements. Lower your overall cost of investment and maintenance by automating your business. Our easy-to-use solution can help you double plant output, eliminate human errors, and increase the efficiency of your production planning process. Manage, track and monitor the complete production process to eliminate unplanned downtime and increase throughput. OEE charts and graphs are dynamically updated with performance and quality data in real-time. -
50
ins2outs
ins2outs
ins2outs is a cloud-based SaaS integrated compliance management platform that empowers organizations to define, operate, and maintain multiple management systems, such as quality, information security, privacy, environment, and AI, within a single unified environment by combining powerful software, pre-built “know-how” sets mapped to standards like ISO 13485/21 CFR 820, ISO 27001, ISO 27701, IEC 62304, and ISO 42001, and expert consulting services. It helps organizations build structured documentation, including policies, processes, procedures, instructions, and document templates, and manage workflows with automated role-based training, push notifications, compliance KPIs, configurable documentation logic, version control, and audit trails, all hosted securely in the cloud. Users can operate integrated systems that address multiple regulatory and standard requirements, manage electronic documentation collaboratively with traceability and export options.Starting Price: $25 per month
