Applicant,Filling,In,Company,Application,Form,Document,Applying,For,Job,

Good Documentation Practices

Overview

Course Description

The objective of this course is to provide the student with a good understanding and the best practices for medical device documents, documentation, and record keeping known as Good Documentation Practices through hands-on experiences.

Participants will also acquire knowledge about essential principles related to Good Documentation Practices (GDPs) for data record elements and standards for maintaining quality documentation.

At The End Of The Course You Will Be Able To

  • Develop general understanding of what Good Documentation Practices (GDPs) are and why they are relevant for the Medical Devices Industry to ensure compliance to the quality system.
  • Learn about key concepts of GMPs for data records elements such as:
    • Data Accuracy
    • Data Integrity
    • Precision
    • Time
    • Legibility
    • Identifiability
  • Learn about Good Documentation Standards and the best practices for:
    • Creation
    • Approval
    • Signatures
    • Handwritten Entries
    • Document modification, corrections and review.
  • Apply GDP requirements and gain knowledge to solve multiple real case situations through out the class.

Course Content

  1. What are Good Documentation Practices.
  2. Data Record Elements:
    • Data Accuracy
    • Data Integrity / Validation
    • Time
    • Legibility
    • Identifiable
  3. Good Documentation Standards
    • Creation
    • Approval
    • Signatures
    • Handwritten Entries
    • Corrections
    • Review

Description

Learn about the key elements of Good Documentation Practices for the medical device industry and their application in managing documentation and records.

Duration: 4 hours

CEUs: 0.5 hours

Modality: Group

Participant limit: 15

Download Course Technical Information

There are no reviews yet.

Only logged in customers who have purchased this product may leave a review.

Course Features

Learn about the key elements of Good Documentation Practices for the medical device industry and their application in managing documentation and records.

Duration: 4 hours

CEUs: 0.5 hours

Modality: Group

Participant limit: 15

Download Course Technical Information

Ask for help

info@smdlearning.com

The Students Also Bought

Introduction to Statistics is a practical course that provides students with a hands-on understanding of basic statistical tools.

Duration: 4 hours

CEUs: 0.5

Modality: Group

Participant limit: 15

Download Course Technical Information

Learn the key concepts and fundamentals associated with the process validation cycle, such as VMP, EQ, TMV, OQ and PQ, and the correlation with regulations and standards.

Duration: 4 hours

CEUs: 0.5 hours

Modality: Group

Participant limit: 15

Download Course Technical Information

Learn about of the Code of Federal Regulations Title 21, Part 820, Understanding FDA Quality System Regulation and process to develop, manufacture and control a medical device product.

Duration: 6 hours

CEUs: 0.7 hours

Modality: Group

Participant limit: 15

Download Course Technical Information

Learn an overview of medical device industry facts, types of medical device products, regulations and product market process submission.

Duration: 4 hours

CEUs: 0.5 hours

Modality: Group

Participant limit: 15

Download Course Technical Information