Mastering DHF, DMR & DHR Training Course: Essential FDA Documentation for Medical Devices (ONLINE EVENT) - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Mastering DHF, DMR & DHR - Essential FDA Documentation for Medical Devices (February 3, 2026)" training has been added to ResearchAndMarkets.com's offering.

Medical device manufacturing is not an easy process. If anything goes wrong, the entire batch of products is at stake. Is there any solution to it? DHF, DMR, and DHR are the three Ds of medical device that needs to be managed carefully.

Even though these files serve different purposes, it is essential to understand how they are mutually inclusive for effective technical documentation. This seminar offers a deeper insight into the documentation part of medical device manufacturing. Moreover, the seminar will cover the latest requirements proposed by FDA and European Union.

Let's dive deeper into the topics covered!

Course Overview

Breaking down each of these terms for a better understanding of freshers into medical device manufacturing:

• Design History File (DHF): Includes an entire history of the device's design, which justifies the currently approved design.
• Device Master Record (DMR): Associated with device production and highlights the requirements like material, equipment, and surroundings.
• Device History Record (DHR): Contains production-related documents which consist of dates, quantity, and labels of final products.

It is essential to have proper knowledge of technical documentation because these are submitted to the FDA. Additionally, these play an important role in pre-market approval of the device. It is crucial for regulatory compliance and this course focuses on future trends and the typical table of contents.

The core purpose of this seminar is to highlight the general safety and performance requirements. Moreover, the coach pays special attention to the file auditing process by FDA and notified the body to make the execution of the concept easier for professionals.

This live training seminar includes the following for each registered attendee:

• A copy of the presentation slides by download
• A certificate of attendance can be downloaded from the WCS Learning Portal following the event
• Q/A Session with the Faculty
• Free Handouts on Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR)

How to Attend

All live training programs audio and visuals are delivered via Go to Webinar with a basic system requirement of a computer with internet access. You do not require a Go to Webinar account to join live training courses, participants receive an email invitation that provides the access you need to join the meeting.

Who Should Attend:

• Quality and Research Analysts: Learn to verify regulatory compliance efficiently and maintain accurate documentation in accordance with FDA and ISO standards.
• R&D Professionals: Understand how to incorporate Design History Files (DHF) and Device Master Records (DMR) when making innovative changes to devices.
• Engineering Teams: Gain insights into device design and mechanisms to ensure proper documentation and regulatory alignment.
• Production / Manufacturing Professionals: Learn to estimate project timelines and align the manufacturing process with Device History Records (DHR) requirements.
• Marketing Professionals: Acquire a clear understanding of the product's development and compliance processes, enabling effective marketing strategies grounded in accurate device knowledge.

Key Topics Covered:

Session 1

• Introduction
• Design Control Under 21 CFR 820.30
• Design and Development Planning under ISO 13485:2016 7.3
• The U.S. FDA's DHF
• The EU MDR's D&DPF
• MDR's "General Safety and Performance Requirements"
• Device Classification - U.S. FDA vs. EU MDD
• Design Files' "Typical" Contents
• The DMR and DHR / Lot / Batch Record TD Expected Contents

Session 2

• Risk Management / File Under ISO 14971
• Narrative
• Hazzard Analysis
• FTA
• D-, P-, and U-FMECA's
• Report

Session 3

• Human Factors / Use Engineering Under IEC 62366-1:2015
• The User Interface
• The 9 Stages
• The HF / UE File

Session 4

• Putting It All Together
• Design Control
• The Team
• Concurrent Compilation of the Three Files
• Derivative Documents Development
• Completion
• FDA and NB Audit Focus
• Final Q&A

Speakers:

John E Lincoln
Principal
J. E. Lincoln and Associates LLC

John E. Lincoln is Principal of J. E. Lincoln and Associates LLC, a consulting company, with over 32 years experience in U.S. FDA-regulated industries, 18 of which as a full time independent FDA-regulated industry consultant. Mr. Lincoln has worked with companies from start-up to Fortune 100, in the U.S., Mexico, Canada, France, Germany, Sweden, China and Taiwan. He specializes in quality assurance, regulatory affairs, QMS / CGMP audits and problem remediation and FDA responses, new / changed product 510(k)s, process / product / equipment including QMS and software validations, ISO 14971 product risk management files / reports, Design Control / Design History Files, Technical Files. He's held positions in Manufacturing Engineering, QA, QAE, Regulatory Affairs, to the level of Director and VP (R&D).

In addition, he has prior experience in military, government, electronics, and aerospace. He has published numerous articles in peer reviewed journals, conducted workshops and webinars worldwide on CAPA, 510(k)s, risk analysis / management, FDA / GMP audits, validation, root cause analysis, and others. He is a graduate of UCLA.

For more information about this training visit https://www.researchandmarkets.com/r/1w4qtl

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