{"id":16999,"date":"2024-08-30T14:16:20","date_gmt":"2024-08-30T14:16:20","guid":{"rendered":"https:\/\/kanboapp.com\/streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors\/"},"modified":"2024-08-30T14:16:20","modified_gmt":"2024-08-30T14:16:20","slug":"streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors","status":"publish","type":"page","link":"https:\/\/kanboapp.com\/en\/streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors\/","title":{"rendered":"Streamlining Drug-Device Combination Product Approvals: A Guide to Regulatory Affairs and Process Management for Associate Directors"},"content":{"rendered":"<style> @media(min-width:1728px) { .tytulek{font-size:45px!important;margin-right:auto!important;margin-left:auto!important;max-width: 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.tytulek{font-size:34px!important;margin-right:auto!important;margin-left:auto!important;max-width: 1200px!important;} .sekcja-tekst { margin-left: 16px!important; margin-right: 16px!important;}  .artykul{margin-bottom:80px!important; margin-top:30px!important;} .menu-lewe a:hover { background:#E9F4FE!important; font-weight:600!important; font-size:16px!important; cursor:pointer!important; } .menu-lewe a { background:#FAFAFA; padding:10px 16px; border-radius: 10px; display: inline-block; outline: none; color:#0C3658!important; font-weight:600!important; font-size:16px!important; }  .kolumna-tekst{flex-basis:100%!important;} .naglowek-duzy {margin-bottom:40px!important; margin-top: 40px!important; font-size:25px!important; font-style:normal; font-weight:700!important; letter-spacing:-0.02em!important; line-height:1.2!important;} .naglowek-maly {margin-bottom:20px!important; font-size:16px!important; font-style:normal; font-weight:700!important; letter-spacing:-0.02em!important; line-height:1.2!important;} .naglowek-start {margin-bottom:40px!important; margin-top: 0px!important; font-size:19px!important; font-style:normal; font-weight:700!important; letter-spacing:-0.02em!important; line-height:1.2!important;} .tekst-para {font-size:16px!important;} .spis { display:none!important; } } .link a:hover { text-decoration:underline!important; } .banner { margin-top:80px; margin-bottom:80px; } .jazda { position:sticky!important; top: 185px; overflow: auto; max-height: 70vh; }  .fobrazek { margin-bottom: -40px!important; } .sekcja5-przycisk a:hover { background: linear-gradient(0deg, rgba(0, 0, 0, 0.15), rgba(0, 0, 0, 0.15)), #ED4B9E!important; }  .sekcja5-przycisk a:focus { background: linear-gradient(0deg, rgba(0, 0, 0, 0.15), rgba(0, 0, 0, 0.15)), #ED4B9E!important; } .vlp-layout-blogs .vlp-block-0 {font-weight: 600!important; } .ct-container-narrow {max-width: 1200px!important;}  <\/style><script> function lewemenu(zm) { var elements = document.getElementsByClassName(\"menu-lewe\"); var i,link1,link2; for (i = 0; i < elements.length; i++) {    link1 = elements[i].getElementsByTagName(\"a\");     link1[0].style.fontWeight = \"600\";     link1[0].style.backgroundColor= \"#FAFAFA\"; } link2 = elements[zm].getElementsByTagName(\"a\"); link2[0].style.fontWeight = \"600\"; link2[0].style.backgroundColor= \"#E9F4FE\"; } <\/script><div class=\"wp-block-getwid-section alignfull alignfull getwid-margin-top-none getwid-margin-bottom-none getwid-section-content-full-width\"><div class=\"wp-block-getwid-section__wrapper getwid-padding-top-none getwid-padding-bottom-none getwid-padding-left-none getwid-padding-right-none getwid-margin-left-none getwid-margin-right-none\" style=\"min-height:100vh\"><div class=\"wp-block-getwid-section__inner-wrapper\"><div class=\"wp-block-getwid-section__background-holder\"><div class=\"wp-block-getwid-section__background\"><\/div><div class=\"wp-block-getwid-section__foreground\"><\/div><\/div><div class=\"wp-block-getwid-section__content\"><div class=\"wp-block-getwid-section__inner-content\"><div class=\"wp-block-columns alignfull artykul is-layout-flex wp-container-core-columns-is-layout-f96e3eba wp-block-columns-is-layout-flex\" style=\"margin-top:0px;margin-bottom:0px\"><div class=\"wp-block-column paskek-lewy spis is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:270px\"><div class=\"wp-block-columns jazda is-layout-flex wp-container-core-columns-is-layout-995f960e wp-block-columns-is-layout-flex\"><div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\"><p class=\"has-text-align-left has-link-color wp-elements-ce7ce8fee1e672e130d03df3c959d2c6 wp-block-paragraph\" style=\"margin-left:10px;font-size:clamp(16.293px, 1.018rem + ((1vw - 3.2px) * 0.68), 25px);font-style:normal;font-weight:600;letter-spacing:-0.01em;line-height:1.2\">Table of Contents<\/p><p class=\"has-link-color wp-elements-23e8f37cb9a7807d17e87dd57c49f32d wp-block-paragraph\"><p class=\"menu-lewe has-link-color\" onclick=\"lewemenu(0)\"><a href=\"https:\/\/kanboapp.com\/en\/streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors\/#section1\" data-type=\"URL\" data-id=\"https:\/\/kanboapp.com\/en\/streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors\/#section1\"  style=\"font-size:clamp(14px, 0.875rem + ((1vw - 3.2px) * 0.391), 19px);font-style:normal;font-weight:600;line-height:1.2;color:#0c3658\">Introduction<\/a><\/p><\/p><p class=\"has-link-color wp-elements-31da6064ee8a5a030b140616a56d556c wp-block-paragraph\"><p class=\"menu-lewe has-link-color\" onclick=\"lewemenu(1)\"><a href=\"https:\/\/kanboapp.com\/en\/streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors\/#section2\" data-type=\"URL\" data-id=\"https:\/\/kanboapp.com\/en\/streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors\/#section2\"  style=\"font-size:clamp(14px, 0.875rem + ((1vw - 3.2px) * 0.391), 19px);font-style:normal;font-weight:600;line-height:1.2;color:#0c3658\">KanBo: When, Why and Where to deploy as a Process Management tool<\/a><\/p><\/p><p class=\"has-link-color wp-elements-86c39a2a3abb95715609b673a81cd102 wp-block-paragraph\"><p class=\"menu-lewe has-link-color\" onclick=\"lewemenu(2)\"><a href=\"https:\/\/kanboapp.com\/en\/streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors\/#section3\" data-type=\"URL\" data-id=\"https:\/\/kanboapp.com\/en\/streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors\/#section3\"  style=\"font-size:clamp(14px, 0.875rem + ((1vw - 3.2px) * 0.391), 19px);font-style:normal;font-weight:600;line-height:1.2;color:#0c3658\">How to work with KanBo as a Process Management tool<\/a><\/p><\/p><p class=\"has-link-color wp-elements-6550222deb418f5018a5ad4ade3674cb wp-block-paragraph\"><p class=\"menu-lewe has-link-color\" onclick=\"lewemenu(3)\"><a href=\"https:\/\/kanboapp.com\/en\/streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors\/#section4\" data-type=\"URL\" data-id=\"https:\/\/kanboapp.com\/en\/streamlining-drug-device-combination-product-approvals-a-guide-to-regulatory-affairs-and-process-management-for-associate-directors\/#section4\"  style=\"font-size:clamp(14px, 0.875rem + ((1vw - 3.2px) * 0.391), 19px);font-style:normal;font-weight:600;line-height:1.2;color:#0c3658\">Glossary and terms<\/a><\/p><\/p><\/div><\/div><\/div><div class=\"wp-block-column kolumna-tekst is-layout-flow wp-block-column-is-layout-flow\"><div class=\"wp-block-getwid-section alignfull sekcja-tekst alignfull getwid-margin-top-none getwid-margin-bottom-none getwid-section-content-full-width\"><div class=\"wp-block-getwid-section__wrapper getwid-padding-top-none getwid-padding-bottom-none getwid-padding-left-none getwid-padding-right-none getwid-margin-left-none getwid-margin-right-none\" style=\"min-height:100vh\"><div class=\"wp-block-getwid-section__inner-wrapper\"><div class=\"wp-block-getwid-section__background-holder\"><div class=\"wp-block-getwid-section__background has-background\" style=\"background-color:#fafafa\"><\/div><div class=\"wp-block-getwid-section__foreground\"><\/div><\/div><div class=\"wp-block-getwid-section__content\"><div class=\"wp-block-getwid-section__inner-content\"><h1 class=\"wp-block-heading tytulek\" style=\"margin-bottom:40px;font-size:clamp(21.536px, 1.346rem + ((1vw - 3.2px) * 1.052), 35px);font-style:normal;font-weight:700;letter-spacing:-0.02em;line-height:1.2\">Streamlining Drug-Device Combination Product Approvals: A Guide to Regulatory Affairs and Process Management for Associate Directors<\/h1><h2 class=\"wp-block-heading naglowek-duzy\" id=\"section1\" style=\"margin-bottom:40px;font-size:clamp(16.293px, 1.018rem + ((1vw - 3.2px) * 0.68), 25px);font-style:normal;font-weight:700;letter-spacing:-0.02em;line-height:1.2\">Introduction<\/h2><p class=\"tekst-para wp-block-paragraph\">Process Management, in the context of the role of an Associate Director for Regulatory Affairs specializing in Drug-Device Combination Products, is an integral framework that ensures all regulatory processes are optimized, efficient, and compliant with the strict industry standards. This approach involves a thorough understanding and management of the myriad processes that drive the development, approval, and post-market surveillance of combination products.<\/p><p class=\"tekst-para wp-block-paragraph\">An Associate Director in this role utilizes process management to marshal resources effectively, maintain alignment with regulatory guidelines, and achieve strategic objectives. By focusing on the continual improvement of processes such as document submission, regulatory strategy development, and cross-functional coordination, an Associate Director ensures that every step taken complies with both domestic and international regulations.<\/p><p class=\"tekst-para wp-block-paragraph\">Process management for an Associate Director in Regulatory Affairs transcends mere adherence to procedures; it involves the anticipation of regulatory trends, strategic planning to navigate complex regulatory pathways, and effective communication to bridge the gap between scientific innovation and regulatory compliance. These efforts lead to a smoother pathway for bringing combination products to market and maintaining their lifecycle, ultimately contributing to patient safety and public health.<\/p><h3 class=\"wp-block-heading naglowek-duzy\" id=\"section2\" style=\"margin-bottom:40px;font-size:clamp(16.293px, 1.018rem + ((1vw - 3.2px) * 0.68), 25px);font-style:normal;font-weight:700;letter-spacing:-0.02em;line-height:1.2\">KanBo: When, Why and Where to deploy as a Process Management tool<\/h3><p class=\"tekst-para wp-block-paragraph\">What is KanBo?<\/p><p class=\"tekst-para wp-block-paragraph\">KanBo is a versatile process management platform that integrates with Microsoft's suite of products, designed to provide real-time visualization of workflows, task and project management, and communication features to streamline coordination and productivity within organizations.<\/p><p class=\"tekst-para wp-block-paragraph\">Why should an Associate Director - Regulatory Affairs (Drug Device Combination Products) use KanBo?<\/p><p class=\"tekst-para wp-block-paragraph\">KanBo facilitates the intricate processes involved in the regulatory affairs of drug-device combination products. It offers structured workspaces, customizable card systems for task management, and compliance with data security standards. The tool enhances team collaboration, tracks project timelines, and streamlines document handling, which is vital in a highly regulated environment.<\/p><p class=\"tekst-para wp-block-paragraph\">When is it appropriate to use KanBo?<\/p><p class=\"tekst-para wp-block-paragraph\">KanBo is particularly useful when managing complex projects that require cross-functional collaboration, regulatory compliance, and strict adherence to deadlines. This includes activities such as submitting regulatory filings, coordinating research and development, managing submission timelines, and ensuring all stakeholders are informed and engaged throughout the regulatory process.<\/p><p class=\"tekst-para wp-block-paragraph\">Where can KanBo be implemented?<\/p><p class=\"tekst-para wp-block-paragraph\">KanBo can be implemented in any work environment that benefits from structured project management and collaboration tools\u2014whether it is on-premises, in the cloud, or in a hybrid setup. Its integration with Microsoft-based environments means it can be adopted in settings where Office 365 or SharePoint are already in use, providing a seamless addition to existing workflows.<\/p><p class=\"tekst-para wp-block-paragraph\">Why should an Associate Director - Regulatory Affairs (Drug Device Combination Products) use KanBo as a Process Management tool?<\/p><p class=\"tekst-para wp-block-paragraph\">As an Associate Director in Regulatory Affairs, overseeing drug-device combination products requires meticulous attention to detail, adherence to multiple regulatory standards, and effective coordination between departments. KanBo's ability to create a transparent workflow, its real-time updating of task statuses, and document management capabilities ensure that regulatory submissions are accurate and deadlines are met. Additionally, KanBo's communication features enable effective alignment with internal teams and external agencies, ensuring that all regulatory requirements are efficiently managed and documented throughout the product lifecycle.<\/p><h3 class=\"wp-block-heading naglowek-duzy\" id=\"section3\" style=\"margin-bottom:40px;font-size:clamp(16.293px, 1.018rem + ((1vw - 3.2px) * 0.68), 25px);font-style:normal;font-weight:700;letter-spacing:-0.02em;line-height:1.2\">How to work with KanBo as a Process Management tool<\/h3><p class=\"tekst-para wp-block-paragraph\">Instruction for Associate Director - Regulatory Affairs (Drug Device Combination Products): Using KanBo for Process Management<\/p><p class=\"tekst-para wp-block-paragraph\">1. Setting Up a Workflows Space in KanBo<\/p><p class=\"tekst-para wp-block-paragraph\">   <\/p><p class=\"tekst-para wp-block-paragraph\">   - Purpose: To establish a centralized platform to visualize and manage the regulatory processes of drug-device combination products.<\/p><p class=\"tekst-para wp-block-paragraph\">   - Why: This provides clear visibility on the status of various regulatory compliance activities, enables monitoring of key processes, and ensures that all team members are updated on procedural changes and compliance requirements.<\/p><p class=\"tekst-para wp-block-paragraph\">2. Constructing and Customizing Workflow Cards<\/p><p class=\"tekst-para wp-block-paragraph\">   - Purpose: To detail each step of the regulatory process in individual cards, allowing for precise tracking of actions and documentation.<\/p><p class=\"tekst-para wp-block-paragraph\">   - Why: Cards act as actionable items that capture critical information, deadlines, and tasks, which ensure that regulatory requirements are met in a timely and organized manner.<\/p><p class=\"tekst-para wp-block-paragraph\">3. Implementing Card Statuses for Process Stages<\/p><p class=\"tekst-para wp-block-paragraph\">   - Purpose: To categorize tasks by their status (e.g., Awaiting Review, In Approval, Completed) for quick identification of process stage.<\/p><p class=\"tekst-para wp-block-paragraph\">   - Why: Statuses allow for immediate recognition of progress and bottlenecks within the regulatory process, facilitating rapid response and continuous flow.<\/p><p class=\"tekst-para wp-block-paragraph\">4. Utilizing Card Relationships for Process Dependencies<\/p><p class=\"tekst-para wp-block-paragraph\">   - Purpose: To link tasks that are dependent on each other to outline sequential order and prioritize actions.<\/p><p class=\"tekst-para wp-block-paragraph\">   - Why: Understanding dependencies is essential to ensure that the process flows logically and that prerequisites are completed before moving on to subsequent steps.<\/p><p class=\"tekst-para wp-block-paragraph\">5. Setting Dates and Reminders on Cards<\/p><p class=\"tekst-para wp-block-paragraph\">   - Purpose: To enforce strict timelines for regulatory submissions and compliance activities.<\/p><p class=\"tekst-para wp-block-paragraph\">   - Why: Regulatory affairs for drug-device combination products are time-sensitive. Deadlines must be adhered to in order to avoid costly delays and maintain market access.<\/p><p class=\"tekst-para wp-block-paragraph\">6. Leveraging Card Grouping for Process Segmentation<\/p><p class=\"tekst-para wp-block-paragraph\">   - Purpose: To organize process steps by categories such as regulatory milestones, submission phases, or product lines.<\/p><p class=\"tekst-para wp-block-paragraph\">   - Why: Grouping helps to keep processes orderly and makes it easier to manage multiple products or submission streams concurrently.<\/p><p class=\"tekst-para wp-block-paragraph\">7. Monitoring Progress with the Forecast Chart<\/p><p class=\"tekst-para wp-block-paragraph\">   - Purpose: To visualize and forecast the completion of regulatory processes.<\/p><p class=\"tekst-para wp-block-paragraph\">   - Why: Anticipating process duration and identifying potential delays ahead of time are crucial for resource planning and meeting submission deadlines.<\/p><p class=\"tekst-para wp-block-paragraph\">8. Reviewing Process Efficiency with Card Statistics<\/p><p class=\"tekst-para wp-block-paragraph\">   - Purpose: To analyze process performance and identify areas for improvement.<\/p><p class=\"tekst-para wp-block-paragraph\">   - Why: Regular analysis of card lifecycle and turnaround times assists in optimizing processes for efficiency and effectiveness.<\/p><p class=\"tekst-para wp-block-paragraph\">9. Conducting Regular Process Review Meetings<\/p><p class=\"tekst-para wp-block-paragraph\">   - Purpose: To discuss process performance, share updates, and implement improvements based on team feedback and statistical analysis.<\/p><p class=\"tekst-para wp-block-paragraph\">   - Why: Continual process evaluation and adaptation maintain alignment with best practices and regulatory changes, which are common in the dynamic field of drug-device combination products.<\/p><p class=\"tekst-para wp-block-paragraph\">10. Using Space Templates for Standard Processes<\/p><p class=\"tekst-para wp-block-paragraph\">   - Purpose: To create templates for standard regulatory processes that can be replicated for different products or regions.<\/p><p class=\"tekst-para wp-block-paragraph\">   - Why: Templates save time on setup, ensure consistency across processes, and uphold compliance standards by aligning with regulatory guidelines.<\/p><p class=\"tekst-para wp-block-paragraph\">Conclusion<\/p><p class=\"tekst-para wp-block-paragraph\">Process management using KanBo allows the Associate Director - Regulatory Affairs to efficiently oversee the intricate regulatory processes pertinent to drug-device combination products. By implementing these steps in KanBo, the Associate Director can ensure that processes are transparent, streamlined, and compliant with industry regulations, ultimately contributing to the organization's strategic goals of quality, efficiency, and regulatory adherence.<\/p><h3 class=\"wp-block-heading naglowek-duzy\" id=\"section4\" style=\"margin-bottom:40px;font-size:clamp(16.293px, 1.018rem + ((1vw - 3.2px) * 0.68), 25px);font-style:normal;font-weight:700;letter-spacing:-0.02em;line-height:1.2\">Glossary and terms<\/h3><p class=\"tekst-para wp-block-paragraph\">Here is a glossary of key terms related to process management, regulatory affairs, and KanBo functionalities, excluding any specific references to a company:<\/p><p class=\"tekst-para wp-block-paragraph\">1. Associate Director - Regulatory Affairs (Drug Device Combination Products):<\/p><p class=\"tekst-para wp-block-paragraph\">   An individual in a leadership role responsible for ensuring that drug-device combination products meet all regulatory standards before gaining approval for market release.<\/p><p class=\"tekst-para wp-block-paragraph\">2. Process Management:<\/p><p class=\"tekst-para wp-block-paragraph\">   A strategic management approach focused on the design, operation, control, and continuous improvement of organizational processes.<\/p><p class=\"tekst-para wp-block-paragraph\">3. Drug-Device Combination Products:<\/p><p class=\"tekst-para wp-block-paragraph\">   Products that combine drugs, devices, and\/or biological products, requiring adherence to complex regulations governed by varying entities depending on the product's primary mode of action.<\/p><p class=\"tekst-para wp-block-paragraph\">4. KanBo:<\/p><p class=\"tekst-para wp-block-paragraph\">   A digital platform designed to assist in task and project management by providing tools for real-time workflow visualization, document handling, and team collaboration.<\/p><p class=\"tekst-para wp-block-paragraph\">5. Workspace:<\/p><p class=\"tekst-para wp-block-paragraph\">   A digital area within KanBo that organizes a specific project, team, or topic's spaces.<\/p><p class=\"tekst-para wp-block-paragraph\">6. Space:<\/p><p class=\"tekst-para wp-block-paragraph\">   Within KanBo, a collection of cards that visually represent a workflow, arranged to manage tasks and projects.<\/p><p class=\"tekst-para wp-block-paragraph\">7. Card:<\/p><p class=\"tekst-para wp-block-paragraph\">   The elemental unit within KanBo representing individual tasks or items requiring action or tracking.<\/p><p class=\"tekst-para wp-block-paragraph\">8. Card Status:<\/p><p class=\"tekst-para wp-block-paragraph\">   An indication of the current phase or condition of a task within KanBo, such as \"To Do,\" \"In Progress,\" or \"Done.\"<\/p><p class=\"tekst-para wp-block-paragraph\">9. Card Activity Stream:<\/p><p class=\"tekst-para wp-block-paragraph\">   A chronological log in KanBo that captures every action and update pertaining to a particular card.<\/p><p class=\"tekst-para wp-block-paragraph\">10. Card Blocker:<\/p><p class=\"tekst-para wp-block-paragraph\">   An impediment listed on a KanBo card that prevents the completion or progress of the task it represents.<\/p><p class=\"tekst-para wp-block-paragraph\">11. Card Grouping:<\/p><p class=\"tekst-para wp-block-paragraph\">   The organization of cards in KanBo based on criteria such as status, assignee, or due date.<\/p><p class=\"tekst-para wp-block-paragraph\">12. Card Issue:<\/p><p class=\"tekst-para wp-block-paragraph\">   Problems associated with a KanBo card that may interfere with task management.<\/p><p class=\"tekst-para wp-block-paragraph\">13. Card Relation:<\/p><p class=\"tekst-para wp-block-paragraph\">   Dependencies between cards in KanBo that relate to the workflow or project structure.<\/p><p class=\"tekst-para wp-block-paragraph\">14. Card Statistics:<\/p><p class=\"tekst-para wp-block-paragraph\">   Analytical data in KanBo showing the progression and life cycle of a card via charts and summaries.<\/p><p class=\"tekst-para wp-block-paragraph\">15. Dates in Cards:<\/p><p class=\"tekst-para wp-block-paragraph\">   Deadlines and milestones assigned to tasks within KanBo to help manage project timelines.<\/p><p class=\"tekst-para wp-block-paragraph\">16. Completion Date:<\/p><p class=\"tekst-para wp-block-paragraph\">   The date on which a card's status in KanBo is set to completed.<\/p><p class=\"tekst-para wp-block-paragraph\">17. Default Parent Card:<\/p><p class=\"tekst-para wp-block-paragraph\">   In KanBo, when a task is dependent on multiple larger tasks (parents), one is chosen as the main or default for greater clarity in hierarchy.<\/p><p class=\"tekst-para wp-block-paragraph\">18. Forecast Chart View:<\/p><p class=\"tekst-para wp-block-paragraph\">   A visualization within KanBo for tracking and forecasting project progress based on past work velocity.<\/p><p class=\"tekst-para wp-block-paragraph\">19. Gantt Chart View:<\/p><p class=\"tekst-para wp-block-paragraph\">   A space view in KanBo that displays tasks on a timeline for improved planning and visibility of project schedules.<\/p><p class=\"tekst-para wp-block-paragraph\">20. Grouping:<\/p><p class=\"tekst-para wp-block-paragraph\">   In KanBo, a method of categorizing cards by related characteristics such as owner, due date, or custom fields for better organization.<\/p><p class=\"tekst-para wp-block-paragraph\">21. List:<\/p><p class=\"tekst-para wp-block-paragraph\">   A type of custom field in KanBo used to categorize tasks into one exclusive category for more straightforward organization.<\/p><p class=\"tekst-para wp-block-paragraph\">These terms provide a common vocabulary for discussing process management as it pertains to project and task coordination within a digital platform like KanBo, particularly in the context of regulatory affairs for drug-device combination products.<\/p><div style=\"height:120px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div><\/div><\/div><\/div><\/div><\/div><\/div><div class=\"wp-block-column paskek-prawy spis is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:270px\"><div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-995f960e wp-block-columns-is-layout-flex\"><div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\" style=\"padding-left:16px\"><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>","protected":false},"excerpt":{"rendered":"","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-16999","page","type-page","status-publish","hentry"],"blocksy_meta":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - 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