Recording Online Training: Full-day pre-course session Audit Trail Review - Im Auftrag der ECA Academy

Recording Online Training: Full-day pre-course session Audit Trail Review - Im Auftrag der ECA Academy

Kosten

ECA-Member*: EUR 790,--
Regular Fee*: EUR 890,--
EU/GMP Inspectorates*: EUR 445,--
APIC Member Discount*: EUR 840,--

Alle Preise zzgl. MwSt.

* auch unkompliziert per Kreditkarte bezahlbar American Express Visa Mastercard

Rückfragen unter:
Tel.: 06221 / 84 44 0 E-Mail: info@concept-heidelberg.de

Sprecher

Bob McDowall, R.D. McDowall Ltd.
Yves Samson, Kereon

Zielsetzung

  • You will learn the current regulatory requirements and regulatory expectations for an audit trail (review)
  • All GMP-relevant data (changes and deletions) should be audit trailed – you will learn how to identify GMP-relevant data
  • Event and audit logs: you will understand the differences between and what the regulators expect
  • How should an audit trail review be performed? You will get familiar with the content and the frequency of an audit trail review

Hintergrund

Audit Trail Reviews are required by international regulations like US 21 CFR Part 11 and EU GMP Guide Annex 11. Clause 9 requests:
“Consideration should be given, based on a risk assessment, to building into the system the creation of a record of all GMP-relevant changes and deletions (a system generated “audit trail”). For change or deletion of GMP-relevant data the reason should be documented. Audit trails need to be available and convertible to a generally intelligible form and regularly reviewed”.

Regulators focus on the (creation), modification and deletion of (GMP-relevant) data while many IT systems are not able to generate audit trails at all or they are not able to generate audit trails for GMP-relevant data.

Therefore, this Online Training is designed to support you to identify GMP-relevant data and how to perform and document an Audit Trail review as part of a second person Review.

Zielgruppe

This Online Training is designed for managers and staff from health care industries as well for auditors who are responsible for the organisation and execution of audit trail (reviews) in their companies.<

Technical Details

To participate in an on demand training course or webinar, you do not need any software. The recordings are made available via a streaming server. In general, the recording is provided in MP4 format, which any PC (Microsoft Windows, Apple IOS) or tablet can easily display.
 

Timing and Duration:

When you register for the on demand Training course or webinar you can decide at what date you want to follow the training course online. For a 1-day training course you will have 2 days in which the stream is available (for 2-day training course 3 days and for a 3-day training course 4 days). Within in this timeframe you can start & stop the stream according to your needs.

In time before the scheduled date (your desired date) you will receive an e-mail from us with a link for direct participation as well as your log-in data.

Training Course Documentation and Certificate:

The presentations will be made available as PDF files via download shortly before the online training course. After the event, you will automatically receive your certificate of participation.

Programm

Why Is An Audit Trail and Its Review Important? 
  • Part 11 and Annex 11 / Chapter 4 requirements for audit trail
  • Regulatory requirements for audit trail review
  • Guidance documents for audit trail review
  • Do I really need an audit trail?
Audit Trail vs. System Log
  • Audit trail content
  • Log files
  • What and when should I review?
  • Meaningful audit trails for a meaningful review
Case Study / Faciliated Discussion: Which Audit Trail to Review?
Attendees will be presented with an overview of the audit trails within an application and the content of each one .  Which audit trails should be reviewed and when?
 
What are GMP-relevant Data?
Annex 11 requires that audit trails monitor GMP-relevant data – what are GMP-relevant data?

Case Study / Faciliated Discussion: Identifying GMP Relevant Data 
Attendees will be presented with a list of records to identify if they are GMP records and how critical they are to help focus the second person review of audit trail data.Examples from production, laboratory and QA examples of GMP relevant data will be provided

Review of Audit Trail Entries
  • Guidance for frequent is “frequent review” of audit trails
  • Process versus system: avoiding missing data integrity issues when only focussing on a per system review
  • What are we looking for in an audit review?
  • Suspected data integrity violation - What do we need to do?
Case Study / Faciliated Discussion: Reviewing Audit Trail Entries
Attendees will be provided with the output of an audit trail to review and see if any potential issues are identified for further Investigation.
 
Technical Controls to Aid Second Person Review of Audit Trails
  • Technical considerations for audit trail review e.g.
  • Identifying data that has been changed or modified – how the system can help
  • Documenting the audit trail review has occurred
  • Review by exception – how technical controls can help
  • Have you specified and validated these functions?

Recording from 31.08.2021
Duration of the recording: 5 h 17 min

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