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{ "item_title" : "Making Agile Native to Design Control", "item_author" : [" Devin Mack "], "item_description" : "Medical device and SaMD teams face a persistent conflict: Agile moves fast, but FDA design controls and EU MDR requirements demand documented, traceable, audit-ready evidence at every step. Most organizations resolve this tension by retrofitting compliance after each sprint - creating a hidden tax of rework, audit scrambles, and release delays that adds 20-40% to total development effort.Making Agile Native to Design Control eliminates the retrofit entirely. Drawing on 25+ years of design quality engineering experience across FDA inspections, EU MDR submissions, and SaMD development programs, author Devin Mack presents the Regulated Sprint Framework - a proven methodology that embeds ISO 14971 risk management, IEC 62304 software lifecycle requirements, and FDA 21 CFR 820/QMSR design controls directly into sprint ceremonies, Definition of Done criteria, and team workflows.This is a working reference for quality engineers, regulatory affairs professionals, software teams building SaMD, and consultants who need compliance to be a natural output of development - not a last-minute deliverable.Inside you'll find: The Regulated Sprint Framework mapped to FDA QMSR, EU MDR, and ISO 13485Sprint-level integration of ISO 14971 risk files, SOUP management, and design traceabilityPCCP (Predetermined Change Control Plan) planning for AI/ML SaMDPractical RACI matrices, SOPs, and design control templates ready for inspectionEU MDR GSPR compliance crosswalks and PRRC accountability structuresReal-world 483 patterns and how sprint-native design control prevents themWhether you are preparing for an FDA inspection, navigating EU MDR technical documentation, or building a quality management system that actually scales with Agile velocity, this book gives you the framework, the tools, and the regulatory rationale to make it work.", "item_img_path" : "https://covers1.booksamillion.com/covers/bam/9/79/899/478/9798994787700_b.jpg", "price_data" : { "retail_price" : "83.00", "online_price" : "83.00", "our_price" : "83.00", "club_price" : "83.00", "savings_pct" : "0", "savings_amt" : "0.00", "club_savings_pct" : "0", "club_savings_amt" : "0.00", "discount_pct" : "10", "store_price" : "" } }
Making Agile Native to Design Control|Devin Mack

Making Agile Native to Design Control : The Regulated Sprint Framework for FDA and EU MDR Compliance

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Overview

Medical device and SaMD teams face a persistent conflict: Agile moves fast, but FDA design controls and EU MDR requirements demand documented, traceable, audit-ready evidence at every step. Most organizations resolve this tension by retrofitting compliance after each sprint - creating a hidden tax of rework, audit scrambles, and release delays that adds 20-40% to total development effort.

Making Agile Native to Design Control eliminates the retrofit entirely. Drawing on 25+ years of design quality engineering experience across FDA inspections, EU MDR submissions, and SaMD development programs, author Devin Mack presents the Regulated Sprint Framework - a proven methodology that embeds ISO 14971 risk management, IEC 62304 software lifecycle requirements, and FDA 21 CFR 820/QMSR design controls directly into sprint ceremonies, Definition of Done criteria, and team workflows.

This is a working reference for quality engineers, regulatory affairs professionals, software teams building SaMD, and consultants who need compliance to be a natural output of development - not a last-minute deliverable.

Inside you'll find:

  • The Regulated Sprint Framework mapped to FDA QMSR, EU MDR, and ISO 13485
  • Sprint-level integration of ISO 14971 risk files, SOUP management, and design traceability
  • PCCP (Predetermined Change Control Plan) planning for AI/ML SaMD
  • Practical RACI matrices, SOPs, and design control templates ready for inspection
  • EU MDR GSPR compliance crosswalks and PRRC accountability structures
  • Real-world 483 patterns and how sprint-native design control prevents them

Whether you are preparing for an FDA inspection, navigating EU MDR technical documentation, or building a quality management system that actually scales with Agile velocity, this book gives you the framework, the tools, and the regulatory rationale to make it work.

This item is Non-Returnable

Details

  • ISBN-13: 9798994787700
  • ISBN-10: 9798994787700
  • Publisher: Enqual LLC
  • Publish Date: March 2026
  • Dimensions: 9 x 6 x 0.83 inches
  • Shipping Weight: 1.19 pounds
  • Page Count: 404

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