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    • Home
    • Engineering
      • Services Overview
      • CAD Drafting Services
      • Computer-Aided-Design
      • Prototyping
      • Machine/System Design
      • Controls / Electrical
      • Pneumatics
    • 3D Printing
    • Machining
    • Quality & Regulatory
      • User Requirement Spec.
      • Functional Design Spec.
      • Metrology
    • Automation & Assembly
      • Low Volume Manufacturing
      • Manual Assembly
      • Extrusion Frames & Assys
    • Industries
      • Med Device & Life Science
    • Contact
Adaptive Industries
  • Home
  • Engineering
    • Services Overview
    • CAD Drafting Services
    • Computer-Aided-Design
    • Prototyping
    • Machine/System Design
    • Controls / Electrical
    • Pneumatics
  • 3D Printing
  • Machining
  • Quality & Regulatory
    • User Requirement Spec.
    • Functional Design Spec.
    • Metrology
  • Automation & Assembly
    • Low Volume Manufacturing
    • Manual Assembly
    • Extrusion Frames & Assys
  • Industries
    • Med Device & Life Science
  • Contact

User Requirement Specification (URS)

Clear, Compliant, and Actionable: User Requirement Specification (URS) Writing Services
Turn Project Goals into Engineering-Ready Requirements

A well-written User Requirement Specification (URS) is the foundation of any successful project—bridging the gap between stakeholder expectations and technical execution.

Find out more

Why Our URS Services Stand Out

Our Speciality

We specialize in writing accurate, audit-ready URS documents that define what your system must do—before design or development begins. Whether you're sourcing equipment, validating software, or implementing new processes, our URS services help ensure you get exactly what you need—on time, on budget, and in full compliance.

Structured, Precise, and Traceable

  • Clearly defined functional, operational, and regulatory requirements
  • Easy-to-audit format aligned with GxP, FDA, ISO, or internal quality standards

Stakeholder-Driven, Engineer-Ready

  • We translate business goals into actionable, testable requirements
  • Ensure alignment between users, engineering teams, and vendors

Experienced in Regulated & Technical Environments

  • Biotech
  • Medical devices
  • Manufacturing automation
  • Custom equipment

Integrated with Your Validation Lifecycle

  • URS documents ready for design qualification (DQ), FAT/SAT, and validation protocols
  • Reduce rework, scope creep, and miscommunication with clear documentation up front

When You Need a URS

Procuring new equipment or systems

Upgrading legacy systems under compliance

Developing custom machinery or software

Developing custom machinery or software

Upgrading legacy systems under compliance

Developing custom machinery or software

Upgrading legacy systems under compliance

Upgrading legacy systems under compliance

Upgrading legacy systems under compliance

Kicking off a GxP-validated project

Upgrading legacy systems under compliance

Upgrading legacy systems under compliance

Don’t leave your project open to interpretation. Start with a URS that sets clear expectations—and builds a path to success.

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