Medical Device Design History File (DHF)

Device Design History File (DHF), mandated by the Safe Medical Devices Act, is a critical document that outlines the design history of a finished medical device. Freyr offers expertise in DHF preparation and remediation, ensuring compliance with Regulatory requirements.

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Medical Device Design History File (DHF) Overview

A Design History File (DHF) is a document that describes the design history of a finished Medical Device. The Medical Device Design History File (DHF) is a part of regulation introduced in 1990, when the U.S. Congress passed the Safe Medical Devices Act, which established new standards for Medical Devices that can cause or contribute to the death, serious illness, or injury of a patient. It is necessary to focus on two aspects of the definition:

  • Defining which records comprise the DHF
  • Focus on the Start and End Points of DHF

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Most of the Regulatory agencies have not specifically provided the exact document content requirements, but following are the high-level contents of a Design History File (DHF) for Medical Devices , which are generally accepted by the agency reviewers or auditors along with other required elements:

  • Design plan
  • User needs
  • Design inputs
  • Design outputs
  • Risk analysis, including hazard identification
  • Human factors analysis
  • Design verification, with acceptance criteria
  • Design validation, with acceptance criteria
  • Design changes
  • Software validation—if applicable
  • Design reviews
  • Design transfer

Freyr makes it easier to compile your Medical Device Design History File (DHF)  or carry out DHF remediation, as per the requirements of target health agencies, like, the US FDA (21 CFR Part 820) or ISO certified notified bodies. The DHF regulations allow Medical Device companies to present their DHF as a document that references the product development documentation for your Medical Device.

Key Interpretations of the DHF Guidance Include:

  • A Medical Device Design History File (DHF) must be maintained for each type of device manufactured by the company. If there are similar versions of the same device with similar design, its recommended to include all the data in a single DHF
  • A DHF is critical to demonstrate that the device was developed in accordance with both the design plan and the requirements. In the whole process, design plan must reflect compliance and it is an important part of the DHF. It must either contain or refer to the necessary documents from where the information is sourced. This means that you could either create a folder that contains the required documents or create a document that acts as a reference sheet for the required materials.

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Medical Device Design History File

  • End-to-end solution for your needs Regulatory needs regarding DHF for medical devices
  • Regulatory support during design and development phase as well as in the lifecycle stage of the product
  • Preparation of all DHF documentation including support for Design Plan, Risk Analysis and Human Factor Analysis
  • Support through complete design landscape covering DHF of medical devices, Design Master Record and Design History Record based on the level of support desired from client
  • Expert resources in DHF preparation and remediation with focused capabilities in specific device categories
  • End-to-end solution on device design aspects starting from gap analysis, development and implementation of remediation plan
  • Dedicated support for design related Regulatory support throughout lifecycle

For end-to-end regulatory support on DHF, reach out to Freyr