Alternatives to iPassport

isoTracker Quality Management is a popular cloud-based quality management software (QMS) system. It is used on a worldwide basis by businesses to manage their ISO 9001, ISO 13485, ISO 22000, ISO 17025, ISO 14001 systems...plus many others. It is a modular product which can be configured to meet an organization's specific requirements and is competatively priced with superg customer support. Any module combination of Document Control, Complaints, CAPA, Audits, Training, Non-Conformance and Risk can be subscribed to.

Adaptive Compliance Engine® (ACE®) is a highly configurable, workflow based eQMS/eDMS and more that can adapt to any business process, allowing for real-time tracking, management, and reporting of all compliance, quality, and operational activities. With ACE®, you will minimize the administrative hassles and maximize ROI with productivity gains from day one – all while 21 CFR Part 11 compliant. Our one-stop software includes: -Office 365 Integration -Inspection Management -Document Management -Risk Management -Product Lifecycle Management -Learning Management -Audit Management -Quality Events -Paperless Validation -Electronic Signatures (21 CFR Part 11 Compliant) -Endless Workflow Configurations -And so much more! Empower all levels of your organization with intuitive user interfaces, easily search for all your documents and records, and transform your data into actionable intelligence with advanced analytics all on a single platform. ACE comes with everything you need, all included at one price. Every application is included, no more a la carte pricing. No more nickel and diming. One software, endless solutions.

QBench allows you to keep track of all your samples and where they are located in the workflow using a single system. QBench eliminates the need for spreadsheets, shared folders in the network, and paper-based tracking systems. You can view hundreds of PDF reports/COAs before publishing or emailing. You can generate barcodes and create labels that you can customize for your samples. Compatible with standard printers and scanners. QBench's billing module allows you to create and send invoices right from the system. You can see counts and latencies for different data types in QBench. This includes metrics like turnaround time, sample counts per test, sample delay, and many others. QBench makes it easy for you to gather the data your lab needs for the assays you perform.

Dot Compliance offers the industry's first ready to use Quality Management Solution powered by the Salesforce.com platform. The Dot Compliance solution includes an extensive set of off-the-shelf ready eQMS and compliance pre-configured processes, enabling customers to deploy quickly and cost effectively. Dot Compliance ready to use solutions include full project validation services and product validation packages. Dot Compliance offers the industry’s most cost-effective quality and compliance management solution available, allowing users to quickly deploy flexible and scalable solutions. Automate core quality processes such as Document Management, Training Management, CAPA, Audits, Customer Complaints, Change Management, Supplier Quality, and more. Our solution is fully configurable and offers seamless integration abilities, with easy adaptation and implementation of customer’s specific requirements.

TLM QMS Software is a powerful and robust quality, risk and material management software (QMS) which is validated and 21 CFR Part 11 compliant. TLM is a cutting-edge, all-in-one quality management system that can be customized to integrate with online CRM software, QuickBooks or ERP databases. Total Lean Management (TLM) QMS Software is specifically intended to be a low cost, highly integrated, flexible and continuously improving landscape to which specialty systems can be added where needed to create the digital business landscape that enables work flows the way your company needs them to work.

The SBS QMS Suite consists of 5 software modules that work together for efficient Quality compliance: SBS Quality Database - CAPA / 8D corrective and preventive actions (CAR) with root cause analysis - Nonconformance management - Risk analysis including FMEA, SWOT, interested party risk register - Internal, customer, and third-party audit management - Environmental Health and Safety (EHS / HSE) management SBS Ground Control - Employee training management (LMS) - Self-Paced training - Document control SBS Asset Tracking Database - Calibrated equipment control - Preventive maintenance - Asset inventory management SBS Inspection Database - Record incoming material, in process, and final product inspection data - Generate real time SPC charts - Inspection plans and Control Plans - Archive data for further statistical analysis SBS Vendor Management - Maintain an approved vendor list or AVL - Develop vendor / supplier qualification plans - Maintain vendor / supplier qualification history Modules may be purchased separately or in any combination.

SimplerQMS offers a cloud-based Quality Management Software, specifically designed for the Life Science industry. SimplerQMS 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, and ICH Q10, among others. The system is fully validated according to GAMP5. The system offers a range of Life Science QMS modules such as Document Control, Change Control, Training Management, Supplier Management, Complaints Management, Non-Conformance and Deviation Management, CAPA Management, Audit Management, Technical Documentation Management, Risk Management, Quality KPIs and more. SimplerQMS integrates with Microsoft Office and allows users to work with documents in applications such as Word, PowerPoint, and Excel. Overall, SimplerQMS delivers efficient, paperless workflows that align with the compliance requirements of the Life Science industry.

Unify quality processes with QT9's all-in-one cloud-based QMS Software Suite. QT9 QMS is a user-friendly quality management software that includes 25+ modules with unlimited scalability. Automate ISO & FDA Compliance with email alerts, To Do lists and FDA 21 CFR Part 11 Compliant Electronic Approvals. QT9 QMS enables Life Sciences, Biotechnology Companies, Medical Device Manufacturers and Pharmaceutical Companies to digitally transform operations. Get real-time status updates and visualize quality metrics up-to-the-minute. QT9 QMS comes with built-in document control, revision-level controls, corrective actions (CAPAs), Nonconforming products and more. Advance product releases with Deviation Management, Engineering Change Orders, FMEA, Inspection Management Modules Included. Go paperless & put time-consuming tasks on autopilot. QT9 QMS comes ready-to-use. Get a free product tour! Start a Free Trial. Visit QT9qms.com

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

All-in-One LIMS, ELN, QMS, and DMS Platform Xybion LIMS is an all-inclusive Digital Laboratory system including LIMS, ELN, QMS, and DMS that creates optimized workflows for the unique business needs of all regulated laboratories including research, diagnostics, quality control, stability studies, and more. Xybion LIMS instills consistency, improves data quality, and supports regulatory compliance with a complete laboratory management solution that connects with your operating systems with powerful laboratory information management and analytics.

BPAQuality365, a QMS software, can be used in your secure Microsoft 365 cloud. It leverages tools used daily by collaborators and does not require you to change your user habits. It is modern, compatible with all devices, adaptable to your specific needs, and powered through innovative M365 technologies. The app includes powerful compliance document management, audit, non-conformance, CAPA action, process and process maps, incident, change, risk, FMEA, SWOT, equipment, health, safety, environment modules compliant with ISO 9001, FDA Part 11 and medical regulations. The QMS app integrates with Teams discussions and users can ask the QMS while chatting in Teams and share QMS card with their colleagues. You can go further to achieve your Quality 4.0 goals by combining powerful AI features with best-in-class workflow automation and business intelligence. BPA's Microsoft Preferred status allows you to customize your QMS to meet your needs, share knowledge with your power users, and learn about M365 technologies.

Qualtrax is a quality and compliance software program that can manage and control documentation, automate key business processes, streamline training management, manage external and internal audits, and ensure that critical industry regulations are met in real time. Qualtrax is a valuable resource in highly-regulated industries where compliance with standards such as ISO 17025 and 17020, 13485 and 9001, TNI and GFSI, FDA and FQS are required.

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

Qualio is a one-stop solution for quality and compliance management. It's ideal for growing companies in healthcare and life sciences. Qualio is reliable, affordable and easy to use. It helps companies build life-saving products faster and achieve 100% ISO, GxP and FDA compliance. Qualio makes it easy for companies to manage document control, training and NCRs, audits as well as suppliers, complaints, and other tasks in one platform.

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

A web-based software suite for medical device companies that automates their processes and simplifies regulatory compliance. Modules include Audit Management, CAPA and Complaint Handling. Designed from the start for ISO 13485 compliance and 21 CFR Part 11 compliance.

It can seem like a never-ending series of tradeoffs to bring breakthrough products to market within highly regulated industries. MasterControl's GxP software simplifies workflows, so you don't have to compromise quality for cost or innovation with regulation. Complete and connected meets flexible and fast. MasterControl Quality Excellence transforms quality data and processes to a competitive edge. Modern software is the first step in modernizing your manufacturing operations. MasterControl Manufacturing Excellence, from work orders to production records (EBR/eDHR), to logbooks and work instructions, is the easiest way to digitalize manufacturing.

Electronic Lab Logs keeps track of all maintenance tasks and quality control for your lab instruments, so you are always prepared for audits and inspections. Electronic Lab Logs is a software platform that streamlines laboratory maintenance and quality-control tasks. The platform replaces traditional paper logs, binders and enables labs track maintenance schedules, QC activities and all instruments efficiently, ensuring readiness for inspections and audits. The dashboard centralizes the task management and allows users to prioritize tasks, complete them from a single interface. Administrators can define instruments and tasks to meet the needs of different laboratories. The system allows the attachment of service reports such as preventive and service reports. This facilitates comprehensive documentation. Electronic Lab Logs is a cloud-based service that does not require server installations.

SoftExpert EQM (enterprise quality management software) is the most comprehensive. It assists companies in achieving and maintaining ISO 9001 certification by automating highly interactive quality processes that are tailored to their 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 can also manage supplier relations, customer complaints and quality audits, as well as competence and training, quality controls, quality inspection, and statistical process control, increasing QMS flexibility and robustness.

The Laboratory Management System (LMS), a Medical/Business Management System, is designed to support Laboratory and Clinic processes and administrative processes. It can manage both patient and staff records, as well as forms and work lists, as well as reports. It includes modules for Andrology and Embryology, which can be customized to fit the practice's internal processes. We identified a gap in clinic software's capabilities and what is essential for clinics and laboratories. LMS was developed for Australian clinics and laboratories. It is designed to ensure quality control in accordance with NATA requirements. Additional modules can be added to the application to meet your specific requirements. Software that tracks medications dispensed to patients. It can also be used to manage an inventory of medications, order medication from pharmaceutical suppliers, and create PBS claims for IVF medications.

Paradigm 3 is both a web- and desktop-based platform that helps businesses manage compliance in document control, CAPA compliance, Competency Tracking, Training, and Document Control. The software includes tools such as an event manager to handle customer complaints and incident investigations, as well as tasks sent by e-mail and audit preparations. Paradigm 3 is beneficial to the following industries: Manufacturing, Test Labs, Healthcare, and Service Industries.

These workflows will help you create everything you need for a 510(k), and create quality records for 21 CFR Part 820 when you are ready to sell your device. Built-in tools for creating policies, procedures, or work instructions. With customized quality management reports, you can track non-conformances, deviations and CAPAs. Keep your team trained as you improve and scale your policies, workflows, and procedures. Automate validation testing for devices, apps, web and custom-made software. Reduce the time and resources required for lengthy testing, reporting, approvals, and other tasks. All your policies, procedures, artifacts can be converted into traditional documents for audit review.

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

IMSXpress is a cutting edge document control and quality management software (QMS) solution. IMSXpress Quality Management is easy to use and intuitive. It improves business efficiency while maintaining compliance. The solution offers a plethora of modules, such as document distribution, document control, internal audit, training, management review, Corrective/Preventive Action (CAPA), customer companies, risk management, preventative maintenance, measuring equipment, supplier control, and more.

Small to medium-sized businesses (SMEs) will love the cloud-based Quality Management System software (QMS). TRACKMEDIUM, a monthly subscription service, includes modules such as Audit Management, CAPA and Document Control, Management of Change (NCM), Training Management, and Management of Nonconformance Management. TRACKMEDIUM allows companies to create safer products, increase efficiency, and comply with industry standards such as ISO 9001, 14001, and OSHA while lowering costs. The Audit Management software by TRACKMEDIUM streamlines audit-related tasks. This includes creating standard audit and checklist templates and generating audit plans. It also allows for the generation of audit recommendations and tracking CAPAs through closure.

The complete software for chemical inventory and laboratory management. LabCup offers complete software management systems for research institutions and laboratories. LabCup offers a wide range of functions, including full chemical inventory software, risk assessment/COSHH and equipment booking. LabCup also provides emergency information. LabCup can be customized to your needs. It is cloud-based and available on any device. LabCup was designed for users to reduce administration and automate processes. LabCup automatically pulls chemical data (SDS and GHS, all synonyms and structures, emergency information and much more) and this data is used throughout the system. Every chemical and item is tracked uniquely by barcode/ID. Multiple processes (including COSHH Risk Assessment, Equipment and Room Bookings, Training Records, Digital Fire Registry, purchasing, radioactives and many more)

Modify fields to reflect the realities of your company. Give permissions and set deadlines. Take control of Documents. Evaluate your suppliers. Create a SWOT Matrix. Create Corrective Action Status reports. All the other requirements of the ISO Standard. You will be notified by email or on the panel of due deadlines and notifications whenever you are assigned a task. For better follow-up, record comments and versions. Includes history of changes. It preserves the history of creation, edition, and derivation of collaboration processes. Planning, monitoring, and registration of processes, audits, and procedures. Attach documentation and evidence. Optimizing time, cost reduction, visualization, interaction and interactivity of processes, methods for follow-up, timely resolutions of problems. These are just a few of the many benefits of digitizing your management systems with inblue QMS.

CompliantPro Quality Management System Software ensures that a company's quality assurance needs are documented in one integrated system. This eliminates silos of information that can be managed as point solutions. CompliantPro allows organizations to manage their compliance and regulatory requirements beyond document control. The key areas are Environmental Health & Safety and Enterprise Risk Management, Training & Qualifications Audits, Customer / Supplier Management.

ApolloLIMS is a robust lab information management system (LIMS), specifically designed for toxicology and pain management laboratories of all sizes. ApolloLIMS, the flagship product of Common Cents Systems allows users to seamlessly manage workflows from specimen accession to results reporting. The core components of ApolloLIMS include customer service, quality control, specimen processing and management reports.

HQMS applications, available on-premise or hosted, including Document Control, Audits, Corrective Action, Calibration, Training, Material Nonconformance, PPAP, Project Management, Risk Management and the HQMS Supplier Portal. Robust technical capability, including, configuration, personalization, and customization, with flexible and customizable security options, any HTML5 browser, Single Sign-On, and more. Integration with ERP and other apps. HQMS across several markets, including manufacturing (Aerospace and Defense, Automotive, Consumer Products, Medical Device, Food, Energy, and more), healthcare, retail, non-profits, and government.. Highly secure Document Control, Audits, Corrective Action, Calibration, Training, and the HQMS Supplier Portal with personalization, configuration, customization, and integration.

OurRecords is a cloud-based credential management system that can be used by healthcare, mortgage, and food businesses. OurRecords allows companies to use a single platform for managing and storing verified credentials and records. Top features include supplier/vendor management, workforce prerequisite program, proactive alerts/notifications, document distribution, centralized documentation, and automated reports.

CLIN1 understands the importance of the laboratory to the healthcare industry. We have the laboratory software that you need. We can help you keep your laboratory running smoothly with the functionality required to organize and efficiently complete your daily tasks. Our solution includes the best quality control tools and quality assurance tools. Software and services are available to help make your laboratory and everyday work more efficient and effective. We have the software and configurations you need to create a productive environment for any type of laboratory, whether it is independent, specialized or hospital, research, veterinary, or other. Our solutions will allow you to provide the best information possible for your clients.

QEdge QMS is Enterprise Quality Management Software (EQMS). It optimizes quality and ensures regulatory compliance. Enterprise Quality Management Software (EQMS), reduces the risk for quality process failures, lowers overall costs, and makes organizational processes more compliant. QEdge is an EQMS that allows companies to manage their Quality Management System in a disciplinary regulatory environment. It brings together all quality processes, such as Change Control and Deviation, Investigation and Market Complaints. OOS, OOT and Risk Assessment. Document Control activities, Training Records, and Document Control activities. QEdge, an intuitive and configurable software platform, allows for cross-functional communication and collaboration. It can interface with legacy systems and facilitates error-free, cross functional communication.

HCLAB is a flexible, comprehensive and practical laboratory information system (LIS). It can be easily customized to meet the specific needs of your laboratory. HCLAB is a medical and diagnostic laboratory information system (LIS) that can be used to automate routine tasks. It is suitable for hematology and coagulation, as well as urinalysis and microbiology, as well molecular and anatomical pathology. HCLAB can be scaled to any size laboratory, whether it is a small project site or a large multi-site healthcare organization or university hospital. HCLAB provides end-to-end information management from initial test requests to results reporting and delivery. Smart client workstations from HCL allow clinical staff to access the web and request orders. Tracks and manages samples sent to outside laboratories for testing that isn't done in-house.

FreeLIMS allows laboratories to replace paper notebooks and spreadsheets with a cloud-based Laboratory Information Management System. This allows laboratories to eliminate manual errors, improve data quality, speed up laboratory operations, and reduce turnaround times. Laboratory work has changed from being a small project involving only a few researchers to large-scale projects that involve multiple laboratories across the globe and often hundreds or even thousands of samples. FreeLIMS, a web-based SaaS LIMS system, is a one-stop shop for managing your samples through the entire life cycle. All industries, including biobanks and clinical research, testing, food, and drink, can seamlessly manage their samples, along with full genealogy and chain of custody.

This LIMS system allows for full control over safety and quality control of products and raw materials, production procedures, and environmental indicators. eQMS: The LIMS allows the establishment and implementation a demonstrable traceability. This ensures compliance with legal regulations and adopted standard and greatly facilitates the implementation and daily implementation of regulatory requirements. Modern LIMS systems extend their functionality beyond the laboratory, particularly in the area of quality management. They allow for systematic monitoring and supervision of all resources, and audit of all business units.

Sunquest Laboratory™, the core engine of your laboratory operations, is equipped with comprehensive laboratory workflows and functionality to help you provide value and service to the healthcare community. The integrated laboratory information system, (LIS), can be interoperable with microbiology, anatomic pathology and physician outreach. It also includes blood bank capabilities. You can leverage end-to-end integrated processes such as specimen labels at collection, PPID, and many more. Manage multi-disciplinary, multisite, multilab environments. Collaboration and communication are key to achieving high quality results. Automate lab processes from order to reporting. Single sign-on is a great way to support your security processes. Connect with enterprise EHRs and physician EMRs.

Administrators, Doctors, Receptionists and Laboratory staff all have one easy-to-use management software. Health.NET is a desktop solution that uses SQL Server Database and runs on Microsoft Windows 7/8/10 computers. Services and web modules are written in Java and Ajax. Health.NET is suitable to all healthcare and medical environments. The CORE version allows you to manage your patient archive, medical record, billing management, professional reports and visits, as well as prescriptions management. This software is ideal for specialists, doctors, and medical groups. One software solution that allows you to share and protect medical data as well as administer it. Health.NET Ultimate adds advanced modules to CORE and provides a responsive service for patients, employees, and administration. It is easy to set up and maintain, and assists users in all aspects of a laboratory workflow, from sample registration to management.

Simple LIMS Software, a Microsoft Access-based LIMS software that is affordable for small laboratories, is simple. This LIMS software is simple and can be used in many industries. It is configurable and easy to use and provides rapid deployment options to support small laboratories in their daily operations as well as customer order management. It is an OPEN SOURCE lab information management software that allows for easy organization of your order workflows, and control over your lab documents. We guarantee that you will immediately see the benefits of our LIMS solution for small labs. It will allow them to improve their lab operations and track processing data records.

Audit Manager is a software that supports quality management. It allows digital management of audits and quality controls in all phases: planning, compilation, and collection of evidence through checklists; verification and management for the entire nonconformity process; definition of corrective measures and data monitoring. You can access the calendar to schedule audits and add the relevant information (subject, checklists, lead auditor, coauditor or participants) for each one. Staff, both internal and outside, can be invited via email to consult the audit schedule prepared directly from the app. Once the inspection has been completed, you can generate the audit report as a PDF or Excel file and share it with the Company Management. You can add the archived minutes to the company's document repository.

iDoc is a document management system that is efficient. Automates and controls the documentation process, including distribution, organization policies and standard operating procedures. It is robust and secure in managing document management systems. It also provides real-time visibility. It streamlines all processes, including creation, review, approval, archival, and archival, and supports multiple files in controlled ways. Integration with training management system to assign training and to remove incorrect documents. This ensures accuracy for end-users and tracks compliance. Automated documentation, document retrieval with search/indexing capability, and document archive. You can easily set up labels, descriptions, and tags to help you organize information and keep track of documents. Keeps track of all documents and tracks any changes. This provides an audit trail that reports on documents and data fields.

Automate the identification and resolution of problems in your organization and supply chain. This is one of the most trusted CAPA software applications. It has been trusted by thousands of users worldwide. CAPA Manager corrective actions software automates the assignment of corrective actions, notification, investigation and reporting. It prevents errors in the control of the entire CAPA process from initiation through investigation and closure. CAPA Manager meets all requirements of the most important quality management standards, including ISO 9001, AS9100 and TS 16949. It maintains records of root-cause and corrective actions, and provides pre-defined workflows with approval gates.

Delphic is an innovative LIS that is used by top laboratories. It is supported by a team made up of highly skilled developers and application specialists at Sysmex. Delphic is compatible with all core lab departments. It supports the delivery of quality services to healthcare providers by managing every step of the pre-analytical and analytical process. The Smart Client interface is modern, intuitive and easy to configure. You can create favorites to make it easy to access the most frequently used areas. Standard-based communication between Delphic and external systems like EHR, HIS and CDR, PMS, national monitoring systems, and cancer registries. Connectivity with automation lines, sample routing and POC testing devices, as well as middleware, is possible thanks to a library of more than 250 interfaces. A dashboard that monitors connectivity status is available to ensure maximum uptime.

Plex Quality Management System helps discrete and process manufacturers comply with strict industry and customer requirements. It is a closed-loop digital record system. Ensure predictable, repeatable quality delivery Clear reporting and in-line quality are key to ensuring high quality. With digital quality documentation, the enterprise can meet industry standards and comply with customer regulations. Increase repeat and new business growth through on-time delivery, better supplier management, and customer satisfaction. Quality management is an integral part of your workflows and processes. This reduces quality loss and the risk of recalls or warranty issues. It also improves your brand reputation and customer relations. Plex makes it easy to share quality requirements and documentation in real time across the enterprise. Plex allows you to create process control plans that include detailed inspection instructions and digital checklists.

Our solution is flexible, powerful, and scalable. It can handle 100 to more than 2000 cases per day. We integrate communication standards with your contacts, the interfaces provided from your partners (autoanalyzer slide and cassette printers), management of technical platforms, add on management modules such electronic treatment form, internet payments, non-conformity managing, traceability, automatic distribution to readers, rapid scanning of case requests, and traceability. Our solution incorporates the concept of structure, allowing multiple legal entities to share the technical platforms. It is possible to subcontract examinations for another laboratory through dedicated computer exchanges. Visualized synthetically, patient records can include any media type (echograph files and spreadsheets, documents, photos, videos, etc.).

You can now get all the documents you need quickly and easily, without wasting valuable time and at a very attractive price. Subscription is easy. Just a few clicks and you will be taken to the order subscription screen. Enter your company data, logo, and information about approval. Fill out the forms and implement according to the ISO 9001 requirements. Get control reports and forms with your organization's name and logo. Prepared for external audit. Self-preparation in your own time without the intervention of an external party. The system is available all year round and data can be entered at any time. Don't rush! All the necessary information for a quality management program, including control forms with your company logo. Everything you need to complete the external audit and your ISO quality management program in one place.

STEMSOFT, a leader in medical informatics and a leading provider of end-to-end solutions for information management, regulatory compliance, and quality assurance to cell therapy manufacturers, hospitals-based cell therapy programs and family and public cord-blood banks, is a market leader. We empower healthcare providers by creating innovative software that helps them discover and deliver effective treatment. You can access training programs with proven results and value-added services. Qualified industry experts and resources provide you with the expertise and specialist knowledge that you need. STEMSOFT Certified Partners provide complementary products and services that streamline your daily workflow and help you meet regulatory and accreditation requirements.

QSE SMART is an application for quality, safety and environmental management that was specifically designed for small to medium-sized businesses and projects with 5 to 500 users. QSE SMART is a solid framework that complies to key requirements of ISO9001 and 45001 and simplifies the daily running of your integrated QSE management software. QSE SMART makes ISO practical for your business. QSE SMART is based on a risk-based approach to ISO 31000. It helps you to identify and exploit key information and metrics that support your business goals in regard to quality, safety and environmental management. This includes your objectives and targets as well as management reviews, risk and opportunities, audits, inspections, management reviews, management reviews, risk and improvement, audits, inspections, audits and inspections.

MediaLab's Inspection Proof module allows laboratories to be ready for inspection at all times. Uploading checklists and responding in the web-based portal means there is no need to keep track of paper or other documents. MediaLab's experts have years of experience in inspection. We have the features you need to make your inspections run more smoothly and efficiently. InspectionProof will eliminate the need for binders full of outdated policies, checklists, and standards. InspectionProof digitizes all your checklists and standards, and stores your evidence and responses in the cloud. Upload attachments, link policies and procedures in Document Control, or your own document management software, and more. Checklists can be imported from a variety of accrediting agencies, including CAP or ASHI. InspectionProof can import Excel and CSV checklists from nearly all laboratory accreditation organizations.

FactoryQA is a quality management software that can be used by manufacturers. Software Features 1. Management of Non-Conformance/CAPA 2. Document Control 3. Instructions for Work 4. Inspection sheets 5. Audits 6. Analytics Services: 1. ISO Certification Consultants 2. Workshops for ISO Certification 3. Fractional Quality Management Services