Introducing the new standard for modern eQMS platforms, our solution is designed to transform the way your organization manages its compliance needs. With a focus on automation, coupled with a user-friendly interface, our platform streamlines compliance processes, reducing manual efforts and turning them into hands-off initiatives. Built for scalability and adaptability, our platform grows with your business.
Transform compliance with quality standards from a complex task to a seamless process through our compliance suite. Centralize all critical assets and information in one place, including tasks, documentation, records, and collaborators, ensuring everything you need is easily accessible.
Transform compliance with quality standards from a complex task to a seamless process through our compliance suite. Centralize all critical assets and information in one place, including tasks, documentation, records, and collaborators, ensuring everything you need is easily accessible.
Gain a comprehensive overview of your company’s compliance status. Track the implementation of controls, identify gaps, and distinguish between applicable and non-applicable requirements with ease.
Clearly understand the objectives of each clause to keep your team aligned. Access direct insights from the source to ensure everyone is on the same page.
Ryze generates AI-powered, expert-validated compliance tasks for your organization. Easily view all tasks related to each clause through the clause details page.
Many clauses require accompanying documentation. Access a comprehensive list of all related documents for each clause within the clause details page.
Records are crucial for achieving and maintaining compliance. Centralize and access all records related to each clause to streamline your compliance efforts.
Know who has access to each clause to enable seamless team-wide collaboration. Achieve compliance more efficiently with fewer resources.
Leverage our custom AI-generated, expert-validated compliance tasks to achieve organizational compliance quickly and effectively.
Our tasks are uniquely tailored to your company. During onboarding, you will complete an intake discovery form, providing us with detailed insights into your company and its quality management system. This information is then processed by our proprietary AI model to generate custom and effective tasks specific to your compliance needs. Finally, our team of expert consultants reviews all tasks to ensure they have the maximum impact in achieving compliance before they are rolled out to your organization.
Gain a thorough understanding of each task’s context. Every task is categorized as a record, documentation, information, or training task, accompanied by an in-depth description of the required actions.
Each task includes a specific action, such as reviewing a document in the document control module, adding or modifying records in various modules, or distributing information throughout the organization. The action component features a button that directs you precisely where you need to go within the tool. Once you complete the task, you can easily navigate back to the task page and mark it as complete.
The Core section of Ryze eQMS is designed to optimize your workflow and enhance productivity through automated actions , robust document control and streamlined access control.
Automated actions ensure your team stays on track with managing and maintaining the eQMS effortlessly.
The Actions Hub is a centralized table displaying all actions assigned to you, helping you prioritize tasks critical to the health of the QMS. Examples of these actions include: Reviewing documents that have entered the review stage, a supplier due for a supplier evaluation and much more.
By consolidating these tasks in one place, the Actions Hub ensures you focus on what matters most, enhancing efficiency and maintaining compliance.
To maintain a compliant and effective document control program, each document must follow a specific approval flow. Starting with the draft stage, you can specify the document’s content, related properties, and the people involved in the process.
Next, optionally send the document for review, allowing your team to provide feedback and suggest changes.
Then, submit the document for approval. All approvers will review it and give a final decision, determining whether the document needs revisions or can be made effective.
Finally, once approved, the document becomes effective and is ready for use in production.This lifecycle also includes retiring, archiving, and performing periodic reviews for documents.
Ryze eQMS offers two methodologies for document control: upload format and the Ryze inline editor. Each method serves different needs based on the document’s context.
Upload Format: Suitable for existing documents that don’t change often. It supports DOCX, XLSX, PDF, PPTX, JPG, and PNG files up to 150MB. After upload, you can view the document.
Ryze Inline Editor: Ideal for new or rapidly changing documents, this fully-featured editor allows you to draft documents directly within the tool.
Properties enable you to configure specific details that dictate the document’s lifecycle, allowing your company to customize the flow and behavior of the document and its interactions within your organization.
Every change for every revision is tracked and available for the document’s entire life, ensuring you can understand its history.
All documents have real-time comment capabilities, enabling anyone with access to the document to ask questions, recommend revisions, or communicate other necessary information.
The Workspace is the document hub that displays documents that are not yet effective.
The Master List is the effective document view, showing all documents that are currently effective.
Our Compliance Library offers over 100 document templates for all aspects of compliance. Curated over decades by our team of consultants, you will have access to any document type your company needs. Easily utilize and customize these templates to meet your company’s requirements.
Ryze eQMS offers granular access control using a combination of tags and groups, ensuring that team members have access to only the information they need.
Groups can be associated with tags, people, modules, and clauses to provide all group members with precisely what they need. Groups can also be externally facing, enabling auditors and suppliers to access critical information easily and reducing the time spent curating this information manually.
Tags serve dual purposes: categorization and access control. Public tags allow your organization to categorize information throughout the ecosystem for ease of location, with everyone having access to these tags. Restricted tags, on the other hand, are associated with groups, granting access only to group members. This enables granular control over access to information, such as restricting certain documents to specific teams.
There are two user types: company admins and users. Company admins have full access to everything in the Ryze eQMS platform. Company users, however, must be added to groups, which will grant them access to the information they need.
The Modules section of Ryze eQMS empowers your organization with a suite of intelligent, integrated tools designed to enhance operational efficiency and compliance. Each module, from Supplier Control and CAPA to Training and more, is crafted to streamline processes, automate routine tasks, and provide robust control over essential functions. With centralized hubs for actions and documents, customizable properties, and comprehensive access management, your team can focus on what truly matters. Ryze eQMS ensures that every aspect of your quality management system operates seamlessly, driving continuous improvement and organizational excellence.
The Calibration Module is designed to provide a streamlined and efficient approach to managing all calibration-related activities, ensuring compliance with calibration clauses in widely recognized quality standards such as ISO 9001:2015.
CAPA (Corrective and Preventive Action) is crucial for identifying and resolving issues within any organization. Traditionally, the CAPA process is underutilized, leading to recurring process failures. Our comprehensive CAPA suite ensures that problems are effectively addressed and remedied, turning CAPA into a collaborative, organization-wide effort.
Start by specifying key details such as the type, severity, source, location, and related departments. Use tags to categorize the CAPA or control access to specific departments and groups. Add collaborators who will assist in the process and receive notifications of updates.
Next, work through the containment process with a dynamic flow. Indicate whether containment is needed and, if so, specify the action details and notify relevant team members. Collaborators will document the actions performed during containment, ensuring transparency and accountability.
Perform a thorough root cause analysis using methodologies such as 5 Whys or Fishbone. Upload the results into the tool to provide evidence and inform team members of the findings, ensuring a comprehensive understanding of the issue.
The corrective action plan section offers two options: a multistep collaborative plan or a single-step action.
Multistep Collaborative Plan: Specify actions, descriptions, due dates, and responsible individuals. Track progress and notify responsible parties upon completion of each action.
Single-Step Action: Retrospectively specify actions performed during the corrective action process, maintaining traceability for compliance.
The final step is for collaborators to verify that containment, root cause analysis, and corrective actions have been properly executed. Once verified, the corrective action can be formally closed, ensuring the issue has been effectively resolved and documented.
The Design Control Module in Ryze eQMS is meticulously crafted to manage every aspect of your design process, ensuring compliance with ISO 9001:2015 standards. This module covers design planning, inputs, controls, outputs, and changes, providing a structured approach to design development.
The Compliance and Feedback Module is designed to streamline the management of compliance-related activities and feedback processing. This module ensures adherence to regulatory standards and improves organizational responsiveness to customer and stakeholder feedback. It supports compliance with recognized quality standards such as ISO 9001:2015, facilitating a systematic approach to managing non-conformities, audits, and corrective actions. By centralizing these processes, the module enhances efficiency, accountability, and continuous improvement within the organization.
The Continual Improvement Module is designed to foster a culture of ongoing enhancement within your organization. This module enables the systematic identification, evaluation, and implementation of improvement opportunities, ensuring alignment with quality standards such as ISO 9001:2015. By centralizing improvement activities, it facilitates efficient tracking, analysis, and reporting of initiatives. The module supports the development of action plans, monitoring of progress, and measurement of outcomes, driving sustained excellence and innovation throughout the organization.
The Interested Parties Module is designed to streamline the identification, engagement, and management of all relevant stakeholders. This module ensures compliance with standards such as ISO 9001:2015 by systematically documenting and addressing the needs and expectations of interested parties. It facilitates efficient communication, relationship management, and feedback collection, ensuring that stakeholder interests are consistently considered in organizational decision-making processes. By centralizing these activities, the module enhances transparency, accountability, and collaborative engagement, contributing to overall organizational success and stakeholder satisfaction.
The Issues Module is designed to provide a comprehensive solution for identifying, tracking, and resolving issues within your organization. This module ensures compliance with quality standards such as ISO 9001:2015 by offering a systematic approach to issue management. It enables efficient logging, categorization, and prioritization of issues, along with tracking progress and documenting resolutions. By centralizing issue management, the module enhances visibility, accountability, and timely resolution of problems, promoting continuous improvement and operational excellence across the organization.
The Equipment Maintenance Module is designed to provide a structured and efficient approach to managing all maintenance activities for your equipment and assets. This module ensures compliance with standards such as ISO 9001:2015 by facilitating systematic scheduling, tracking, and documentation of maintenance tasks. It supports preventive and corrective maintenance, enabling you to minimize downtime and extend the lifespan of your equipment. By centralizing maintenance operations, the module enhances operational efficiency, accountability, and the reliability of your assets, contributing to overall organizational performance and safety.
The Management Review Module is designed to facilitate effective and efficient management review processes within your organization. This module ensures compliance with quality standards such as ISO 9001:2015 by providing a structured approach to planning, conducting, and documenting management reviews. It supports the systematic evaluation of performance metrics, strategic objectives, and improvement opportunities. By centralizing management review activities, the module enhances organizational oversight, accountability, and strategic decision-making, ensuring continuous improvement and alignment with organizational goals.
The Quality Objectives Module is designed to facilitate the effective management and achievement of your organization’s quality goals. This module ensures compliance with standards such as ISO 9001:2015 by providing a structured approach to setting, tracking, and evaluating quality objectives. It supports the alignment of objectives with organizational strategy, enabling continuous monitoring and reporting on progress. By centralizing these activities, the module enhances visibility, accountability, and performance management, driving continuous improvement and ensuring that quality objectives are met consistently.
The Risk-Based Thinking Module is designed to embed a proactive approach to risk management throughout your organization. This module ensures compliance with quality standards such as ISO 9001:2015 by systematically identifying, assessing, and mitigating risks. It supports the integration of risk-based decision-making processes, enhancing the organization’s ability to anticipate and address potential challenges. By centralizing risk management activities, the module promotes a culture of continuous improvement, resilience, and strategic foresight, ultimately contributing to the stability and success of the organization.
Traditionally, supplier evaluation and requirement policies are specified in static documents and manually implemented. With Ryze eQMS, you can define the supplier policy and automatically apply it to all suppliers, saving your team time and ensuring all suppliers comply with company-specified policies.
Supplier Management is a dynamic and collaborative module that allows your team to specify details, assess risks, and manage documents for each supplier. Based on the supplier type and risk specifications, the module dynamically requires certain documents, ensuring compliance and saving time. The module includes a seamless supplier approval flow, enabling your team to work together in approving new suppliers and ensuring informed decisions are made when integrating new suppliers into your business processes.
Supplier Evaluation can be seamlessly performed within the Ryze Supplier Control module, allowing your team to easily conduct evaluations with the right information at the right time.
Ensure your team stays on track and no supplier is left behind on their evaluation requirements with automated reminders. These reminders inform key individuals when evaluations need to be performed, ensuring timely and consistent compliance.
The Training and Training Plans Module is designed to streamline the management of employee training and development programs. This module ensures compliance with standards such as ISO 9001:2015 by providing a systematic approach to planning, delivering, and tracking training activities. It supports the creation of personalized training plans, monitoring of progress, and assessment of outcomes. By centralizing training management, the module enhances organizational capability, ensures competency, and fosters a culture of continuous learning and improvement, contributing to overall performance and compliance.
