{"title":"Design Controls, DHF \u0026 Clause 7.3","description":"\u003ch2\u003eDesign Controls, DHF \u0026amp; ISO 13485 Clause 7.3 Toolkits\u003c\/h2\u003e\n\u003cp\u003eStrong design controls are the difference between a defensible medical device development process and a documentation trail that collapses under audit. This collection is built for companies that need to structure, execute, and defend design and development activities in line with ISO 13485 clause 7.3. It brings together practical DHF tools, execution systems, audit-ready examples, and training resources that help teams control the full design lifecycle.\u003c\/p\u003e\n\n\u003cp\u003eWhether you are setting up a new design history file, repairing incomplete development records, formalizing design reviews, or linking design controls to risk management and CAPA, these products are designed to help you create evidence that is usable, traceable, and inspection-ready.\u003c\/p\u003e\n\n\u003ch3\u003eWhat This Collection Helps You Do\u003c\/h3\u003e\n\u003cul\u003e\n  \u003cli\u003eBuild or repair a complete Design History File (DHF)\u003c\/li\u003e\n  \u003cli\u003eControl design planning, inputs, outputs, review, verification, and validation\u003c\/li\u003e\n  \u003cli\u003eImprove traceability between requirements, risk, testing, and approval evidence\u003c\/li\u003e\n  \u003cli\u003eDocument design changes with stronger control and rationale\u003c\/li\u003e\n  \u003cli\u003ePrepare for ISO 13485 audits, FDA inspections, and EU MDR technical review\u003c\/li\u003e\n  \u003cli\u003eTrain teams on clause 7.3 expectations using ready-to-run materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003ch3\u003eIncluded Product Types\u003c\/h3\u003e\n\u003cul\u003e\n  \u003cli\u003eDHF essentials and setup toolkits\u003c\/li\u003e\n  \u003cli\u003eFull design controls execution systems\u003c\/li\u003e\n  \u003cli\u003eFilled examples and audit evidence libraries\u003c\/li\u003e\n  \u003cli\u003eClause 7.3 training kits\u003c\/li\u003e\n  \u003cli\u003eRisk-management-linked design control products\u003c\/li\u003e\n  \u003cli\u003eQMS-in-a-Box products for design-only \/ R\u0026amp;D entities\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003ch3\u003eWho This Collection Is For\u003c\/h3\u003e\n\u003cul\u003e\n  \u003cli\u003eStartup manufacturers developing new devices\u003c\/li\u003e\n  \u003cli\u003eR\u0026amp;D-focused companies without a strong commercial QMS yet\u003c\/li\u003e\n  \u003cli\u003eQA\/RA teams cleaning up incomplete design records\u003c\/li\u003e\n  \u003cli\u003eConsultants preparing clients for certification or inspection\u003c\/li\u003e\n  \u003cli\u003eBusinesses moving from informal development to controlled design execution\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003ch3\u003eWhy Clause 7.3 Needs a Dedicated System\u003c\/h3\u003e\n\u003cp\u003eDesign controls are rarely weak because teams do not know the terminology. They fail because inputs are vague, outputs are not formally approved, verification evidence is disconnected, validation logic is thin, and traceability is incomplete. These toolkits are built to fix that operational gap. They make design work auditable, structured, and much easier to defend.\u003c\/p\u003e\n\n\u003ch3\u003eBuild a Defensible Development System\u003c\/h3\u003e\n\u003cp\u003eIf your product lifecycle depends on stronger design evidence, clearer DHF structure, and better linkage between development, risk, and change control, this collection is where that work starts.\u003c\/p\u003e","products":[{"product_id":"design-control-training-kit","title":"Design Control Training Kit","description":"\u003c!-- Design Control Training Kit --\u003e\n\u003cdiv\u003e\n  \u003ch2\u003eWho This Kit Is For\u003c\/h2\u003e\n  \u003cp\u003e\n    R\u0026amp;D, engineering, QA\/RA and project managers who must understand stage-gated design and development controls for medical devices and IVDs.\n  \u003c\/p\u003e\n\n  \u003ch2\u003eThe Compliance Problem It Solves\u003c\/h2\u003e\n  \u003cul\u003e\n    \u003cli\u003eGaps between design activities and documented requirements of ISO 13485 clause 7.3.\u003c\/li\u003e\n    \u003cli\u003ePoorly evidenced design reviews, verification, validation and design transfer activities.\u003c\/li\u003e\n    \u003cli\u003eNew staff not understanding DHF expectations, traceability and change control during development.\u003c\/li\u003e\n  \u003c\/ul\u003e\n\n  \u003ch2\u003eWhat You Get In This Kit\u003c\/h2\u003e\n  \u003cul\u003e\n    \u003cli\u003eDesign control training slide deck covering plan, inputs, outputs, review, verification, validation and transfer.\u003c\/li\u003e\n    \u003cli\u003eTrainer guide and facilitator notes referencing your Design Control SOP and templates.\u003c\/li\u003e\n    \u003cli\u003eLearner workbook including design case studies and traceability matrix exercises.\u003c\/li\u003e\n    \u003cli\u003eAssessment pack to verify understanding of design control deliverables and responsibilities.\u003c\/li\u003e\n  \u003c\/ul\u003e\n\n  \u003ch2\u003eHow This Kit Reduces Your Audit Risk\u003c\/h2\u003e\n  \u003cul\u003e\n    \u003cli\u003eConnects everyday design work with formal design control requirements and DHF expectations.\u003c\/li\u003e\n    \u003cli\u003eSupports consistent documentation quality across projects, reducing design-related audit findings.\u003c\/li\u003e\n    \u003cli\u003eProvides demonstrable training evidence for personnel involved in design planning, execution and review.\u003c\/li\u003e\n  \u003c\/ul\u003e\n\n  \u003ch2\u003eHow To Implement It (Step-by-Step)\u003c\/h2\u003e\n  \u003col\u003e\n    \u003cli\u003eDownload the kit and integrate examples based on your current or recent design projects.\u003c\/li\u003e\n    \u003cli\u003eDeliver training to all design team members, including QA\/RA reviewers and approvers.\u003c\/li\u003e\n    \u003cli\u003eUse workbook tasks to map real requirements, risks and tests into a sample traceability matrix.\u003c\/li\u003e\n    \u003cli\u003eFile attendance, assessment results and link training status into your Design Control SOP and training matrix.\u003c\/li\u003e\n  \u003c\/ol\u003e\n\n  \u003ch2\u003eTechnical \u0026amp; Regulatory Alignment\u003c\/h2\u003e\n  \u003cul\u003e\n    \u003cli\u003eBuilt for: ISO 13485:2016 clause 7.3; supports alignment with FDA design controls and EU MDR technical documentation requirements.\u003c\/li\u003e\n    \u003cli\u003eTypical use: product development, design changes, sustaining engineering.\u003c\/li\u003e\n    \u003cli\u003eDocument type: Design control training kit.\u003c\/li\u003e\n  \u003c\/ul\u003e\n\u003c\/div\u003e\n","brand":"ISO Cloud Consulting","offers":[{"title":"Default Title","offer_id":46017143898306,"sku":null,"price":69.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0709\/8361\/4658\/files\/Firefly_GeminiFlash_Createasquarepremiumproductthumbnailfor_DesignControlTrainingKit_.Showap74305.png?v=1773429428"},{"product_id":"iso-13485-qms-in-a-box-design-only","title":"ISO 13485 QMS-in-a-Box — Design-Only \/ R\u0026D Entity","description":"\u003cp\u003eDesign-only organizations are often forced into generic QMS models that overbuild manufacturing controls while still leaving Clause 7.3, DHF integrity, and design-transfer logic exposed. This design-only edition hard-locks Clause 7.3 expectations, DHF integrity, and design-transfer boundaries so teams can build an audit-defensible development system without unnecessary manufacturing content. That means less time spent rebuilding documents from scratch and a stronger line of evidence when the process is sampled under audit.\u003c\/p\u003e\u003ch3\u003eWhat's included\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eGovernance and Use Guide.pdf\u003c\/li\u003e\n\u003cli\u003eImplementation Sequence.pdf\u003c\/li\u003e\n\u003cli\u003eRegulatory Role Definitions.pdf\u003c\/li\u003e\n\u003cli\u003eClause Applicability Matrix.xlsx\u003c\/li\u003e\n\u003cli\u003eMandatory vs Optional Records.xlsx\u003c\/li\u003e\n\u003cli\u003eAudit Exposure Risk Map.pdf\u003c\/li\u003e\n\u003cli\u003eInternal Audit Doctrine.pdf\u003c\/li\u003e\n\u003cli\u003eInternal Audit Framework.pdf\u003c\/li\u003e\n\u003cli\u003eInternal Audit Execution Checklists.pdf\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eBest suited to:\u003c\/strong\u003e R\u0026amp;D team, Startup manufacturer, Quality manager, and Regulatory consultant.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUseful in audit situations where you need to:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eShow a structured design-only ISO 13485 implementation process during ISO 13485 certification, surveillance, supplier, or internal audits.\u003c\/li\u003e\n\u003cli\u003eSupport FDA inspections with controlled records, traceability, and process evidence related to design-only ISO 13485 implementation.\u003c\/li\u003e\n\u003cli\u003eSupport EU MDR technical documentation or quality-system reviews where design-only ISO 13485 implementation records need to be complete, controlled, and consistent.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eUse this design-only edition to implement the right controls in the right order and present a cleaner design-control model to certification auditors and investors.\u003c\/p\u003e","brand":"ISO Cloud Consulting","offers":[{"title":"Default Title","offer_id":46615995908290,"sku":"ISO 13485 QMS-in-a-Box — Design-Only \/ R\u0026D Entity","price":1290.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0709\/8361\/4658\/files\/Firefly_Createasquarepremiumproductthumbnailfor_ISO13485QMS-in-a-Box-Design-Only-74305.png?v=1773430797"},{"product_id":"design-history-file-dhf-essentials-toolkit","title":"Design History File (DHF) Essentials Toolkit","description":"\u003cp\u003eMost teams know they need a Design History File, but their records are incomplete, unlinked, or impossible to defend under audit sampling. This toolkit gives you a practical DHF structure, traceability logic, and the minimum document set needed to move from scattered design records to an inspection-ready DHF. That means less time spent rebuilding documents from scratch and a stronger line of evidence when the process is sampled under audit.\u003c\/p\u003e\u003ch3\u003eWhat's included\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eDHF Implementation Guide.docx\u003c\/li\u003e\n\u003cli\u003eDHF Index Template.xlsx\u003c\/li\u003e\n\u003cli\u003eDHF Register.xlsx\u003c\/li\u003e\n\u003cli\u003eDesign Control Audit Checklist.docx\u003c\/li\u003e\n\u003cli\u003eDHF Folder Structure Blueprint.pdf\u003c\/li\u003e\n\u003cli\u003eDHF Remediation Guide.pdf\u003c\/li\u003e\n\u003cli\u003eInspection Preparation Notes.pdf\u003c\/li\u003e\n\u003cli\u003eTraceability Matrix.xlsx\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eBest suited to:\u003c\/strong\u003e Startup manufacturer, R\u0026amp;D team, Regulatory consultant, and Quality manager.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUseful in audit situations where you need to:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eShow a structured Design History File and design controls process during ISO 13485 certification, surveillance, supplier, or internal audits.\u003c\/li\u003e\n\u003cli\u003eSupport FDA inspections with controlled records, traceability, and process evidence related to Design History File and design controls.\u003c\/li\u003e\n\u003cli\u003eSupport EU MDR technical documentation or quality-system reviews where Design History File and design controls records need to be complete, controlled, and consistent.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eUse this toolkit to move faster, create cleaner evidence, and reduce the time it takes to stand up or repair this part of your ISO 13485 system.\u003c\/p\u003e","brand":"ISO Cloud Consulting","offers":[{"title":"Default Title","offer_id":47258387939522,"sku":"Design History File (DHF) Essentials Toolkit","price":129.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0709\/8361\/4658\/files\/Firefly_GeminiFlash_Createasquarepremiumproductthumbnailfor_DesignHistoryFile_DHF_EssentialsT74305_d5fc2905-e994-48d0-8e8f-a9cfae8785f8.png?v=1773429592"},{"product_id":"iso-13485-filled-examples-library-design-controls-audit-and-capa-closure","title":"ISO 13485 Filled Examples Library: Design Controls Audit \u0026 CAPA Closure","description":"\u003cp\u003eA common failure point is not understanding what good evidence actually looks like when auditors sample records, trace design changes, or ask for CAPA closure proof. This library gives you realistic filled examples that show document depth, linkage, naming, and closure quality so your team can model evidence before an audit. That means less time spent rebuilding documents from scratch and a stronger line of evidence when the process is sampled under audit.\u003c\/p\u003e\u003ch3\u003eWhat's included\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eBundle Manifest.pdf\u003c\/li\u003e\n\u003cli\u003eFilled Audit Pack Examples.docx\u003c\/li\u003e\n\u003cli\u003eFilled Design Review Records.docx\u003c\/li\u003e\n\u003cli\u003eFilled Verification Records.docx\u003c\/li\u003e\n\u003cli\u003eDHF Master Index Example.xlsx\u003c\/li\u003e\n\u003cli\u003eCAPA Record Example.docx\u003c\/li\u003e\n\u003cli\u003eEffectiveness Verification Example.docx\u003c\/li\u003e\n\u003cli\u003eAudit and CAPA Trackers.xlsx\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eBest suited to:\u003c\/strong\u003e Quality manager, Regulatory consultant, Startup manufacturer, and Internal auditor.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUseful in audit situations where you need to:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eShow a structured filled examples and audit evidence process during ISO 13485 certification, surveillance, supplier, or internal audits.\u003c\/li\u003e\n\u003cli\u003eSupport FDA inspections with controlled records, traceability, and process evidence related to filled examples and audit evidence.\u003c\/li\u003e\n\u003cli\u003eSupport EU MDR technical documentation or quality-system reviews where filled examples and audit evidence records need to be complete, controlled, and consistent.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eUse this toolkit to move faster, create cleaner evidence, and reduce the time it takes to stand up or repair this part of your ISO 13485 system.\u003c\/p\u003e","brand":"ISO Cloud Consulting","offers":[{"title":"Default Title","offer_id":47258389872834,"sku":"ISO 13485 Filled Examples Library: Design Controls Audit \u0026 CAPA Closure","price":149.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0709\/8361\/4658\/files\/Firefly_GeminiFlash_Createasquarepremiumproductthumbnailfor_ISO13485FilledExamplesLibrary-Des74305.png?v=1773430663"},{"product_id":"design-controls-execution-system-iso-13485-clause-7-3","title":"Design Controls Execution System (ISO 13485 Clause 7.3)","description":"\u003cp\u003eMany medical device companies have partial design-control records but fail to maintain a defendable system linking requirements, reviews, verification, validation, transfer, and change control. This system gives you the complete operating structure for clause 7.3, including templates, execution logic, traceability, and audit-defence support for real design-control implementation. That means less time spent rebuilding documents from scratch and a stronger line of evidence when the process is sampled under audit.\u003c\/p\u003e\u003ch3\u003eWhat's included\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eDesign Controls Operating Manual.pdf\u003c\/li\u003e\n\u003cli\u003eDesign and Development SOP Set.docx\u003c\/li\u003e\n\u003cli\u003eDesign Development Plan.docx\u003c\/li\u003e\n\u003cli\u003eDesign Inputs Specification.docx\u003c\/li\u003e\n\u003cli\u003eDesign Outputs Specification.docx\u003c\/li\u003e\n\u003cli\u003eDesign Review Pack.docx\u003c\/li\u003e\n\u003cli\u003eVerification Pack.docx\u003c\/li\u003e\n\u003cli\u003eValidation Pack.docx\u003c\/li\u003e\n\u003cli\u003eDesign Transfer Pack.docx\u003c\/li\u003e\n\u003cli\u003eDesign Change Control Pack.docx\u003c\/li\u003e\n\u003cli\u003eRisk Linkage Pack.docx\u003c\/li\u003e\n\u003cli\u003eExecution Workbook.xlsx\u003c\/li\u003e\n\u003cli\u003eAudit Traps and Defences.pdf\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eBest suited to:\u003c\/strong\u003e Startup manufacturer, Medical device manufacturer, Regulatory consultant, and Quality manager.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUseful in audit situations where you need to:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eShow a structured design controls process during ISO 13485 certification, surveillance, supplier, or internal audits.\u003c\/li\u003e\n\u003cli\u003eSupport FDA inspections with controlled records, traceability, and process evidence related to design controls.\u003c\/li\u003e\n\u003cli\u003eSupport EU MDR technical documentation or quality-system reviews where design controls records need to be complete, controlled, and consistent.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eUse this system to move faster, create cleaner evidence, and reduce the time it takes to stand up or repair this part of your ISO 13485 framework.\u003c\/p\u003e","brand":"ISO Cloud Consulting","offers":[{"title":"Default Title","offer_id":47258389905602,"sku":"Design Controls Execution System (ISO 13485 Clause 7.3)","price":499.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0709\/8361\/4658\/files\/Firefly_GeminiFlash_Createasquarepremiumproductthumbnailfor_DesignControlsExecutionSystem_ISO74305.png?v=1773429476"},{"product_id":"iso-14971-risk-management-system","title":"ISO 14971 Risk Management System","description":"\u003cp\u003eRisk management is often treated as a document exercise, but auditors expect a living process that links hazards, risk controls, residual risk, and post-market feedback. This system gives you a practical ISO 14971 structure you can use to build and maintain a defendable risk-management file without reinventing the methodology. That means less time spent rebuilding documents from scratch and a stronger line of evidence when the process is sampled under audit.\u003c\/p\u003e\u003ch3\u003eWhat's included\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eRisk Management Policy.docx\u003c\/li\u003e\n\u003cli\u003eRisk Management Plan Template.docx\u003c\/li\u003e\n\u003cli\u003eRisk Management Pre-Analysis Registers.xlsx\u003c\/li\u003e\n\u003cli\u003eRisk Evaluation and Control Workbook.xlsx\u003c\/li\u003e\n\u003cli\u003eRisk Benefit Analysis Worksheet.docx\u003c\/li\u003e\n\u003cli\u003eOverall Residual Risk Approval.docx\u003c\/li\u003e\n\u003cli\u003eRisk Management File Index and Traceability.xlsx\u003c\/li\u003e\n\u003cli\u003ePMS Data Sources and Signal Review.xlsx\u003c\/li\u003e\n\u003cli\u003eRisk Management Report Shell.docx\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eBest suited to:\u003c\/strong\u003e Medical device manufacturer, Quality manager, Regulatory consultant, and R\u0026amp;D team.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUseful in audit situations where you need to:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eShow a structured risk management process during ISO 13485 certification, surveillance, supplier, or internal audits.\u003c\/li\u003e\n\u003cli\u003eSupport FDA inspections with controlled records, traceability, and process evidence related to risk management.\u003c\/li\u003e\n\u003cli\u003eSupport EU MDR technical documentation or quality-system reviews where risk management records need to be complete, controlled, and consistent.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eUse this system to move faster, create cleaner evidence, and reduce the time it takes to stand up or repair this part of your ISO 13485 framework.\u003c\/p\u003e","brand":"ISO Cloud Consulting","offers":[{"title":"Default Title","offer_id":47258390397122,"sku":"ISO 14971 Risk Management System","price":599.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0709\/8361\/4658\/files\/Firefly_GeminiFlash_Createasquarepremiumproductthumbnailfor_ISO14971RiskManagementSystem_.Sho74305.png?v=1773431141"},{"product_id":"free-dhf-audit-checklist-and-index-template","title":"Free DHF Audit Checklist \u0026 Index Template","description":"\u003cp\u003eDesign teams often need a fast way to see whether their DHF is even structurally complete before they buy a larger system. This free checklist-and-index combo captures design-control intent and feeds naturally into the paid DHF essentials and full design-controls system. It is positioned as a practical first step that gives buyers immediate value without forcing them into a full rebuild on day one.\u003c\/p\u003e\u003ch3\u003eWhat's included\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eDesign Control Audit Checklist.pdf\u003c\/li\u003e\n\u003cli\u003eDHF Index Template.xlsx\u003c\/li\u003e\n\u003cli\u003eQuick-Start Guide.pdf\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eBest suited to:\u003c\/strong\u003e Startup manufacturer, R\u0026amp;D team, Consultant, and Quality manager.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eUseful in audit situations where you need to:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eShow a structured DHF structure and design-document review process during ISO 13485 certification, surveillance, supplier, or internal audits.\u003c\/li\u003e\n\u003cli\u003eSupport FDA inspections with controlled records, traceability, and process evidence related to DHF structure and design-document review.\u003c\/li\u003e\n\u003cli\u003eSupport EU MDR technical documentation or quality-system reviews where DHF structure and design-document review records need to be complete, controlled, and consistent.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eDownload it, put it to work immediately, and use it as the entry point into the full paid system when you need deeper control, stronger records, and a broader implementation framework.\u003c\/p\u003e","brand":"ISO Cloud Consulting","offers":[{"title":"Default Title","offer_id":47258391019714,"sku":"Free DHF Audit Checklist \u0026 Index Template","price":0.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0709\/8361\/4658\/files\/Firefly_GeminiFlash_Createasquarepremiumproductthumbnailfor_FreeDHFAuditChecklist_IndexTempl74305.png?v=1773430236"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0709\/8361\/4658\/collections\/Firefly_Gemini_Flash_Create_a_high-trust_website_banner_for_a_Design_Controls_and_DHF_collection_aligned_t_417843.png?v=1773406343","url":"https:\/\/isocloudconsulting.com\/collections\/design-controls-dhf-clause-7-3.oembed","provider":"ISO Cloud Consulting","version":"1.0","type":"link"}