Alternatives to ValGenesis

A cloud LIMS that tracks samples, tests results, and manages inventory for life science research, industrial QC labs, and biotech/NGS. Includes regulatory support for CLIA and HIPAA, Part 11 and ISO 17025. The quality, security, traceability, and traceability for samples is crucial to a lab's success. Laboratory professionals can use the Lockbox LIMS system to manage their samples. They have full visibility of every step of the sample's journey from accession to long-term storage. LIMS analysis is more than just tracking results. Lockbox's multilayered sample storage and location management functionality lets you define your lab's storage structure using a variety location options: rooms and storage units, shelves and racks, boxes and boxes.

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.

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!

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.

Intellect's QMS software has been proven to improve quality operations and reduce overall quality cost by up to 40%. Our apps were designed by certified quality professionals and can be easily customized with our no-code platform or drag-and-drop technology. Remote access for your team, mobile apps, dynamic workflows, analytics, reporting, and remote access are all possible with this modern and simple solution. Apps include Document Control and Employee Training, Audit Management CAPA, Nonconformance, as well as other useful features.

Qualityze EQMS Suite is a next-generation Enterprise Quality Management Software. It is specifically designed for businesses to efficiently manage their quality processes, customer expectations and compliance requirements. It helps them address operational challenges so they can achieve excellence in terms of quality, safety and reliability. It comes with pre-defined templates for controlled documents, audit checklists, regulatory forms, material compliance reports and many more. Qualityze EQMS Suite is a set of 14 integrated modules that help create a closed-loop system to manage end-to-end quality from anywhere. Our range of smarter quality solutions is built on the Salesforce.com technology platform. These modules are Nonconformance Management, CAPA Management, Document Management, Change Management, Audit Management, Training Management, Supplier Quality Management, Inspection Management, Customer Complaints Management, Material Compliance Management, Forms Management, Permit Management, Calibration Management, and Maintenance Management, Forms Management and Field Safety Management. Our Quality Management solutions help create a culture of quality and continuous improvements by proactively mitigating quality issues.

Revolutionize your Life Sciences processes. You can dramatically improve the quality, control, and efficiency of your products and processes. Our fully compliant platform is pre-validated according GAMP5. This ensures inspection readiness at all time. You have complete control over all documents and processes. You can also customize workflows and automate when possible. You can enjoy uninterrupted workflows and full traceability with seamlessly connected and integrated modules. Our dedicated team is available to answer any questions you may have. Only the best Scilife experience is possible! Our Scilife platform automates, automates and organizes all processes in your industry space, no matter if you're in Medical Devices or Pharma & Biotech or ATMP. Click below to see which Scilife modules are available for your industry's unique lifecycle stages.

We offer solutions to companies that have a high standard of quality. Our software solutions are characterized by a modern UX and useful functionality. They also feature high modularity and consistent compliance. Integrated solutions to manage quality and ensure quality. Focused on digitizing controlled documents and QA process. Solutions designed specifically to meet the requirements of the financial sector for written rules of procedure and management of policies. Cloud-based, prevalidated solution for automating your validation processes as well as digitally controlling and managing validation documents. Early setup of a digital quality management system with a solution that is tailored for startups and young businesses. Based on DHC VISION. It is ready to use, with immediate compliance. No license fees. Together, we digitize the quality management and quality control processes and ensure regulatory compliance.

Vault QualityDocs provides automated workflows and audit trails that provide detailed audit trails. This reduces compliance risk and improves quality. It speeds up review and approval and facilitates the sharing SOPs and other GxP documents between employees and partners. Effective SOP management is made easier by automated workflows and visibility to the content status and processes. This reduces compliance risk. An intuitive, user-friendly interface is key to adoption and efficiency. Audit trails with detailed audit trails, content organization, powerful search, and robust search allow for better inspections and audits. You can securely access and use any web browser. If enabled, you can also print, distribute, track, and track the control of PDF copies. Pre-defined metadata and document taxonomy allow for operational harmonization. Organizations can quickly adopt best practices by using pre-defined pick lists for quality, manufacturing and validation documents.

Carizma QM, a web-based software, supports users in managing all aspects of regulated documents, from authoring, review and approval, release, and archiving. Management and creation of regulated documents, e.g. SOPs. Integrated workflows that can be reviewed and approved. After approval, automatic start of training workflow. Read and understood. Electronic signature - 21 CFR Part 11 compliant. Display of users who have understood and read. Audit trail and validation. CarizmaQM supports users in managing the entire lifecycle of regulated documents. Key information is defined by the author, e.g. document type (SOP or work instruction, form, checklist etc. Document title, process owner (department), document type, review cycle, and title. When a document is to be reviewed, users are identified by e-mail. Carizma creates a skeleton document.

Qualis LIMS is an enterprise-grade laboratory information management system that is widely used in various industry verticals, such as pharmaceuticals, life sciences, contract research, clinical research, and analytical and commercial sample testing. This system has integrated modules designed to manage all laboratory processes, enabling labs to perform their tasks in an automated and paperless manner while ensuring compliance with regulatory requirements and industry standards. Qualis LIMS is a digital transformation tool for laboratories, providing the following features: • Efficient management, storage, and aliquoting of samples. • Record keeping of test and experiment results, along with the management of tests, projects, samples, instruments, and inventory in a secure central database. • Compliance with data integrity and regulatory requirements such as GxP, ISO17025, 21 CFR Part 11, and EudraLex Annex 11 without compromising quality.

Virje complies to 21 CFR Part 11, 21 CFR Section 820, ISO 13485. Are you overwhelmed by the idea of Part 11 software validation Accessible wherever you are, whenever you work. Automated collaboration and automation can help you reduce paper, lower costs, and increase efficiency. This is the ideal solution for small- to medium-sized businesses. This system was designed specifically for quality control of medical devices. The system is flexible enough that it can adapt to your workflows without having to compromise. Modifiable change order approvals can be configured by employee role or by document type. Notifications to the responsible personnel at each stage of the change process. Ability to identify material dispositions for individual documents. Access to historical and released versions of documents is easy. Quick access to document history. Tracking of locations and distribution of hard copies. Notification of periodic document 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.

Teamcenter®, a modern product lifecycle management (PLM), system, connects people and processes across functional silos with a digital thread for innovative. You can solve more of the difficult problems required to create high-quality products due to the unmatched breadth of the Teamcenter portfolio. The Teamcenter user interface is simple and intuitive, allowing everyone in the organization to take part in product development. No matter how Teamcenter is deployed - on-premises, cloud, or via TeamcenterX - you will get the same proven solutions that help you innovate faster. Start Teamcenter by gaining control over product data and processes. This includes 3D designs, embedded software, documentation, as well as your bill of material (BOM). Your PLM system will yield greater returns if you leverage your product information across multiple domains and departments.

Our scientists and EHS professionals have extensive experience in managing laboratory safety and risk management. This allows us to address critical problems. BioRAFT understands the need for a platform that simplifies safety tasks, allowing scientists to return to their research. Modules can be added to meet your organization's evolving needs. BioRAFT works with customers to create new functionality. A single, simple-to-use system that increases laboratory safety and efficiency can reduce total operational costs. A robust chemical database makes it easy to manage chemical inventory. Easy generation of complex regulatory reports. Conduct, review, and approve inspections based on hazard criteria. This allows for real-time data analysis dashboards. Provide a comprehensive safety and health training program that includes user-specific assignments, automated requirements, reminders, and more.

Organizations need to standardize their business processes and automate them in order to bring new products to market quickly and comply with global regulations. QUMAS EQMS (formerly ProcessCompliance), a cloud-based solution that provides integrated regulatory, quality and compliance management capabilities within a validated QMS environment, is QUMAS EQMS. QUMAS's data-centric approach lets you manage quality content easily and access and re-use all data. This gives you a comprehensive view into Quality. Interactive quality dashboards from QUMAS provide QMS overviews across all business areas and quality initiatives. Export, email, and scheduling are all possible for reports. QUMAS allows QMS departments the ability to securely, efficiently, and compliantly exchange information in the cloud.

Laboratories must be able to manage large amounts of data accurately to meet strict standards. They also need to constantly improve efficiency, automation, and turn-around time. Autoscribe Informatics' Matrix Gemini LIMMS (Laboratory Information Management System), is designed to meet these specific needs. Configurability vs. customized coding has always been a compromise when choosing a LIMS. Autoscribe Informatics solutions are unique in that they offer genuine configuration capabilities with no custom code. This allows customers to tailor their solution to a wide range laboratory and process requirements. Matrix Configuration Tools offer superior flexibility, which allows for fast implementation and an interface that is easy to use. Easy configuration results in a longer system life and lower cost of ownership.

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.

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.

Software that helps you comply with regulations. Fannie Mae, Wendy's and Walmart trust the best mobile inspection and audit platform. This will help you improve safety and accuracy. The #1 field management platform for teams, FORM OpX will transform your Excel, paper, and digital processes. FORM OpX combines advanced data gathering and configurable workflows with powerful operational insight to increase compliance in real time. To ensure compliance and team compliance, you can set up audits, inspections, or workflows. Digital forms allow you to capture data and guide teams to the right actions. Set up automated alerts and escalates to prompt corrective action when issues arise. You can save time and money by creating customizable workflows that improve processes, increase compliance, and reduce errors.

BIOVIA solutions provide a unique scientific management environment that enables science-based organizations to create and connect biological and chemical innovations that will improve our lives. The BIOVIA portfolio, which is a leader in the industry, focuses on integrating science, experimental processes, and information requirements from all aspects of research, development, quality control, and manufacturing. Capabilities in the areas of Scientific Informatics and Molecular Modeling/Simulation Data Science, Laboratory Informatics Formulation Design, BioPharma Quality & Compliance, Manufacturing Analytics, and Laboratory Informatics. BIOVIA is committed in accelerating innovation, improving productivity, quality and compliance, reducing cost, and accelerating product development for customers across multiple industries. Connect scientific innovation processes and information throughout the product lifecycle.

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)

The AssurX platform is a powerful software platform for enterprise quality management (EQMS) and regulatory compliance to reliably communicate and coordinate information, documentation, and activities. AssurX allows regulated businesses to quickly identify and control quality issues and risk exposure to avoid quality or noncompliance problems while improving workflow. AssurX QMS software is uniquely 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. No other system is easier to deploy, configure, and modify. AssurX solutions integrate seamlessly to create a connected quality system. Solutions include audit management, corrective actions, training management, compliant management, document management, change control, risk management, EHS incident management, and more.

Loftware Prisym 360 offers innovative content management features that incorporate industry best practices. It is specifically designed to meet the complex regulatory requirements for clinical supplies labeling. Many clinical labeling teams use English MLT/CLT variants for defining the content of booklets and labels for clinical trials. The number of countries in each study increases and each country has specific regulatory content, phrases, and language requirements. Therefore, the manual process of designing booklets and printing them takes longer and is more risky. Prisym 360's CLT/MLT solution prompts users to provide study information. Then, it automatically generates MLT, CLT, and booklet designs based on its knowledge about content and design requirements. This reduces the time it takes to create a clinical label or booklet, reduces errors and ensures compliance with regulatory requirements.

To optimize your shop floor, combine manufacturing, MES and supply chain software. Learn how DELMIAworks, formerly IQMS, can help you improve visibility into every aspect your manufacturing operation and solve the most difficult production problems. Reduce downtime and increase manufacturing efficiency, quality, profit margins, and quality. Real-time data access across the entire supply chain can improve decision making. All ERP, manufacturing, MES and supply chain requirements can be handled by one system. Automating your business can lower your investment and maintenance costs. Our simple-to-use solution will double your plant output, eliminate human error, and improve the efficiency of production planning. To eliminate unplanned downtime, increase throughput and reduce downtime, manage, track and monitor all aspects of the production process. OEE graphs and charts are dynamically updated with performance data and quality data in real time.

AmpleLogic's Quality Management Software is designed to meet the strict requirements of industries that are heavily regulated. The ISO 9001-certified cloud-based Quality Management System is ideal for Lifesciences and other industries such as Food & Beverages, Cosmetics, Medical Devices or Gene Therapy. Businesses are adopting QMS solutions as they recognize the challenges of manual quality checks, which can be laborious and prone to errors. These systems are crucial in improving audit quality by automating processes, managing data efficiently, and integrating APIs.

Moonchase has developed Lab Online, a next-generation open-source web-based* platform. It uses state-of the-art technology. This LIS platform, which was developed "from scratch" by a Belgian engineering team that has been involved in this field for over 20 years, supports all aspects of the prescription, execution, and reporting of clinical biology analyses. Lab Online offers more than 70 modules that can be used by all clinical biology laboratory actors (internal or external). These include instrument communication, automated validation, quality control, and on-line consultation of the results in real-time.

Quality Link 7 is a combination of people and technology. It builds on our proven platform to help organizations automate processes, save time, and comply with regulatory requirements. Quality Link's document management system improves efficiency and eliminates the need for manual paperwork. This module will store and manage every document you create. This module allows you to print "uncontrolled" copies and perform other document-related tasks. You'll see a reduction in clerical tasks for quality staff by up to 90% with the improved organization. Our software converts existing documents from your previous management system and requires no learning curve. You won't have to lose your favorite applications as they can be easily integrated. Quality Link makes manual document maintenance obsolete and eliminates the need for constant monitoring.

QLAB is a global service provider of software professionals. QLAB is a research & development (R&D) company that focuses on clinical laboratory information system infrastructure. This allows QLAB to comply with all regulatory agencies. It also provides technical guidance and leadership to other R & D companies. We are committed to improving LIS automation processes using current technologies tools and complying with accreditation agencies' requirements. QLAB is committed to improving the practice and standards for clinical laboratory information systems (LIS). This will optimize functionality, scalability reliability, interoperability, and interoperability. QLAB is committed to achieving a competitive advantage over LIS vendors in terms of cost, support, quality, and quality.

Online appointment scheduling and registration allows you to gather everything you need in advance. You can reach patients via email, text, and chat. Automated reporting for insurance claims. Best-in-class security and privacy standards. Manage vaccines and testing at large scale. This includes scheduling, intake, reporting and follow-up. Accessible via phone/tablet, no app needed. Integration with paperless labs to deliver results instantly. Patients receive confirmations by email and text. Flexible scheduling tool for website events and employer dashboard. State reporting, registry integration, exports for claims processing. Built on a proven enterprise software platform that manages millions of transactions. You can create custom templates to promote your services.

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.

TELCOR RCM billing software can be used by any type of lab: independent reference lab, pathology practice, outreach lab, or public health lab. It will help you overcome billing challenges and increase profitability. All of your revenue cycle management functions can be performed in one solution. This includes claim submission, claim monitoring and remittance processes. Client and patient billing is also possible. The right tools can automate daily billing functions, such as collecting patient information and claims submission. This will reduce the need for billing staffing and increase revenue cycle productivity. You can eliminate manual adjudication and labor-intensive processes by automating electronic payments from payers via 835 ERAs, or from your bank via lockbox file payment files.

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.

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

CodonLIMS integrates an Electronic Lab Notebook (ELN), and Laboratory Information Management System. It can be used in pharmaceutical companies as well as chemical laboratories, mining, stainless-steel manufacturing, petrochemicals, food, fruit & paper industries, etc. It helps to efficiently manage lab information and improve laboratory turnaround times. The application offers a variety of features, including sample tracking and management of multiple aspects. To prove compliance and measure efficiency, laboratory information should be easily accessible. CodonLIMS makes it easy to access information whenever and wherever it is needed. CodonLIMS automates manual processes, facilitates instrument integration and consolidates complex informatics. This allows end-users to share data, information, and increases collaboration across complex areas of research. Can be customized to meet specific lab requirements.

Any laboratory can do their best with clinical information and data management systems. Standard workflows, optimized processes, and high-quality performance can all be used to improve patient care. This lab automation software manages staff, inventory, and high-value work. SumLIMS: Why Choose SumLIMS? 1. It increases the efficiency of the laboratory 2. It ensures that each step of the process is accurately recorded 3. It increases the security of data-related information 4. It is an economical solution for small labs 5. It prevents rework and the associated costs.

1factory's Manufacturing Quality software is cloud-based and on-premises and was specifically designed for manufacturing companies of any size. 1factory's Manufacturing Quality is a reliable and secure solution that allows for first article inspections and factory monitoring. It also provides quality control plans, in process and final inspections, inspection management, CAPAs and non-conformances. Other key features include the ability to calculate Process Performance (Ppt, Ppk), and Process Capability (Cpt, Cpk), variation/SPC control management, defect risk monitoring, and many more.

Try out new ways to manage your data and projects. Laby can adapt to any size organization, no matter how large or small. Join our community and let's create tomorrow's innovations. Organize all your projects, experiments, and essays. Create a recipe to manufacture finished products. Automate the item management and traceability. Manage and supervise laboratory instruments. Laby centralizes all your files onto a single platform, allowing for easy access and retrieval. Prepare and validate quality documentation before distribution. Search, share and consult all scientific publications. Sign reports using EIDAS and 21 CFR part 11. Track time spent on each project and export data. Complete management system that allows for high standards of monitoring. Receive training to save time and get to work faster.

RQM+, a global service provider for medical technology, is focused on accelerating market success and compliance. We deliver specialized solutions to medical technology companies and accelerate the journey along the entire product lifecycle, from concept through commercialization and post-market. Our portfolio of services allows us to deliver end-to-end products and solutions throughout the entire medical device lifecycle. RQM+ quality assurance engineers review materials lists, establish suppliers, and support design change processes. RQM+’s design quality engineers support any packaging, sterility or biocompatibility testing that may be required. RQM+ regulatory affairs consultants offer guidance and assistance with submissions to FDA, notified authorities, or other government agencies. Our extensive experience with the most recent reimbursement requirements and value based compensation models is what we use.

The Ennov platform has its own workflow engine, which provides advanced capabilities. Ennov Training, Ennov eTMF, and Ennov RIM use workflows. They enable the organization to control the sequence of tasks and data modification, while also providing visibility throughout the organization. Functional administrators can configure workflows using a graphical interface. To ensure consistency, coherence checks are performed when you save modifications. Ennov ensures that workflows are consistent and reliable. Each Ennov workflow comes with a configurable form. Dynamic sections allow data entry to be made easier by displaying or hiding fields depending on what field values have been entered (e.g., the type of Incident). The connected user can enter free text, select values from picklists, and add additional files as needed. To complete a workflow step, an electronic signature may be required.

In today's pharmaceutical manufacturing environment, it can be difficult to maintain consistent product quality and quality processes. To meet regulatory requirements, industries like the Pharmaceutical, Biotech and Life Sciences must maintain Good Manufacturing Practices (GMP). You must not only meet GMP requirements, but you must also be capable of proving it.

Defect-free business processes are the key to quality products. CASQ-it was designed to cover all aspects of your quality assurance and management processes, starting with the development phase and continuing through the material processing - including your support processes. The key advantage of CASQ is its process-oriented operation. This functionality allows your CAQ system adapt to your processes, and not vice versa. CASQ-it supports quality assurance processes as they move into the future. Quality and reliability increase customer satisfaction while reducing the cost per unit. Each CASQ-it module can be used independently, allowing you to optimize your individual processes and workflows in your company from the beginning. You can combine our modules to create a complete quality assurance system.

A well-implemented Quality Management System (QMS) is essential for biotech firms to achieve regulatory compliance. It will also help them maintain product quality and safety. It will also help them manage risks effectively. It will drive operational efficiency. InstantGMP QMS was designed by quality and regulatory professionals for biotech companies. It is simple, affordable, and complete. It can be used by small-to mid-sized manufacturers in many different industries. This quality management software features guided workflows to reinforce adherence with government standards during the entire production process. It also has a variety of innovative features and specialized module. Maintain and improve the safety and quality of biotech products. Frameworks are provided for identifying, assessing and mitigating risk throughout the product's lifecycle to reduce the likelihood of quality incidents or product recalls.

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.

Almond is a cloud-based professional quality management software designed for healthcare companies. The software allows for computerized management of quality processes that are in compliance with regulatory requirements. The system maintains an audit trail of documents, indexes all documents and provides documented evidence for all QMS processes. All information is centralized in a single place. This allows you to manage your suppliers easily. You can give your suppliers permission to conduct training at their premises using your quality system, if it is required by your system. Receive automatic emails before the expiration of supplier certification. You can be informed at any time about the status of your project using an electronic control dashboard. You can create as many logbooks you need without any budget or storage restrictions. Automatic conversion from ineffective to effective after training completion.

Pharmaceutical and Biotech companies face challenges in meeting control documentation requirements in their day-to-day operations. Document management and control are essential components of any quality and compliance solution. Global Regulatory agencies expect all regulated companies to follow industry best practices during the manufacturing process. Phama Soft Sol created Document Management System software to help manage and distribute SOP's, STP's, and other regulated documents. Document management software systems can not only lower compliance costs but also improve product quality and process efficiency. Document Management System (softDMS) allows you to quickly retrieve the information you need, at the exact time you need it. This reduces the risk of miscommunications and errors which in turn minimizes risks, manhours, and other documentation errors.

Advantum's flexibility and security make it the perfect solution to your information management needs. You can choose from pre-packaged solutions or individual components. Or, let us design something that is unique to your needs. We will provide cost efficiency, reliability, and custom configurations. It is easy to work anywhere you like today. Advantum can be used on any device, including your smartphone or tablet. Advantum's flexibility allows you to tackle the challenges of today while still being prepared for future technical and organizational changes. Advantum is flexible, as is its licensing model. Flexible licensing is used and we focus on concurrent users. Advantum is a cost-effective option for you by sharing licenses. Our customers appreciate our support the most.

ZipQuality, a software-enabled medical device service, helps companies bring new products to the market. Our collaboration platform allows agile teams to make rapid design changes while maintaining regulatory compliance. System (processes and tool) pre-configured; no need to change your quality system. The integrated system is able to handle rapid design iterations in product documentation. Your team will be guided by experienced consultants at every stage. Software tools that are fully featured, scalable, and built on the powerful ENOVIA platform. Our integrated system allows for rapid design changes, while keeping data and documentation in sync. All records are maintained in a audit-ready condition. Product requirements, Hardware requirements, Software requirements. We have a deep understanding of complex, software-intensive devices. ZipQuality is a structured documentation system that supports good systems engineering and efficient risk management. It also provides clear traceability.

Ideagen Quality Management, a modular SaaS application, is designed with quality managers in mind. More than 6,000 customers trust Ideagen Quality Management to digitalize and comply with industry standards. Ideagen Quality Management integrates seamlessly with your existing processes, and is the backbone of your business. Our system's workflow automation and comprehensive documentation management empowers your team by identifying and resolving any issues before they occur. Our powerful digital quality management software will help you to improve your organization's performance, and give you a competitive advantage. Our software helps you gain full visibility of your organization, identify risks and take action, and maximize opportunities. Secure world-class processes and smart data-driven decisions that will satisfy your customers, regulators, and grow your business.