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Health & care: 21 CFR Part 11 - Compliance for Electronic Records and Signatures

Electronic Records and Signatures,21 CFR Part 11,Health & care,Data science


NetZealous LLC

Summary

Price
£140 inc VAT
Or £46.67/mo. for 3 months...
Study method
Online
Duration
1 hour · Self-paced
Access to content
6 months
Qualification
No formal qualification
Certificates
  • Certificate of completion - Free
Additional info
  • Tutor is available to students

Overview

This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA regulated companies and how conformance to Part 11 differs from just having good IT security.

Procedures for controlling electronic signatures and electronic records as described in the FDA Guidance will be explained.

FDA regulated companies want to transition to electronic records for economy and efficiency. FDA, because of its concern for patient safety, wants to prevent electronic records from being compromised with possible resulting harm to the patient. FDA has set up regulations that address both data security and patient safety. We will show how 21 CFR part 11 considers both.

Certificates

Certificate of completion

Digital certificate - Included

Description

Why you should Attend:

Companies want to transition to electronic records but are afraid of compromising their quality system and receiving 483's at their next inspection. Part of this fear originates from confusion. FDA originally published a rather severe 21 CFR Part 11. After industry complaints the FDA acknowledged that the regulation, as written, would result in nobody attempting to convert to electronic records. But, instead of rewriting the regulation, FDA said it would "selectively enforce" sections of the regulation.

This webinar will explain what all this means. A 21CFR checklist and a Test protocol form will be given as handouts .

Areas Covered in the Session:

  • Origin of the regulation and changes in Interpretation
  • Electronic Records
  • Electronic Signatures
  • Data Security
  • Open, closed and hybrid Systems
  • Validation Methods
  • Risk Analysis

Who is this course for?

  • Engineering Personnel
  • QA
  • IT
  • Management

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FAQs

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