Kom med på holdet
27. November 2018 til 28. November 2018

Kursus: GMP requirements for Computer Systems & Data Integrity

A review of FDA and EU requirements and interpretations relating to computer systems (CS)

Course objective

The aim of the course is to increase participants’ knowledge of:

  • Existing GMP and EU requirements and interpretations relevant to CS
  • Validation of various types of CS, using a risk-based approach
  • Requirements and actual interpretations relating to Electronic Records and Electronic Signatures, based on 21 CFR, Part 11
  • Warning Letters issued in the area of Data Integrity and CS Validation
  • Data Integrity and IT Security


Course description / Who should attend

This course focuses on GMP requirements as they relate to CS, as well as interpretations of and compliance with these requirements. The course is aimed at QA staff and anyone else involved in qualifying/validating CS. The course is also suitable for support staff with a need to familiarize themselves with the IT-specific GMP requirements.

Participation prerequisites

  • Basic training/knowledge in GMP / Quality systems.
  • You should have at least 6-12 months experience from working in GMP regulated industry.

If you are uncertain about your level of basic GMP knowledge, you can buy and take an online testhere »

Course content

Day 1 – THEME: General requirements/CS validation
  • Background for CS validation
  • Relevant GMP requirements, FDA
  • Relevant GMP requirements, EU
  • The “life-cycle model”, risk and CS testing
  • Off-the-shelf software
  • Presentation of validation information for the FDA and the EU
Day 2 – THEME: Part 11 – Electronic Records/Electronic Signatures (ER/ES)
  • Part 11 – Background and Scope
  • Archiving and copying of ER and ES
  • User Access – User Rights
  • Audit Trail, Operational checks and Device checks
  • ES
Day 2 – THEME: Data integrity
  • Background: Definition of Data Integrity (ALCOA)
  • IT Security
  • Protect your data!
  • Electronic Records or hardcopy?
  • IT behaviour
  • Examples of Data-Integrity Warning Letters
  • Wrap-up

Both course days also include a review of relevant warning letters.

Genau Talks

Anna Lundén, training director and part owner, Key2Compliance® and Henrik Johanning, CEO Genau & More, discuss tendencies and developments to be found in observations and warning letters.


Peter Nyborg




27. November 2018 til 28. November 2018



Tietgensgade 65

1704 København V

Kontakt os

For further information please contact Peter Nyborg

Skræddersyede kurser til din virksomhed

Vi tilbyder tilpassede kurser, som tager udgangspunkt i jeres behov og udstyr.

Vores undervisere har mange års erfaring fra pharmaindustrien og har alle deltaget både i inspektioner og interne audits.

Hør mere om mulighederne for netop jer.

Kontakt os

Forespørg på kursus

For at vi kan give dig den mest optimale tilbagemelding, vil det være en hjælp for os, hvis du angiver:

* Skal udfyldes