Computer Systems Validation

  • Subscribe to our RSS feed.
  • Twitter
  • StumbleUpon
  • Reddit
  • Facebook
  • Digg

Monday, 9 January 2012

Definition of Raw Data

Posted on 12:30 by Unknown
Within EU Chapter 4 – Documentation there is a clear definition of Raw Data and the requirements to retain the raw data.

Records: Provide evidence of various actions taken to demonstrate compliance with instructions, e.g. activities, events, investigations, and in the case of manufactured batches a history of each batch of product, including its distribution. Records include the raw data which
Read More
Posted in 21 CFR Part 11, Electronic Records | No comments
Newer Posts Older Posts Home
Subscribe to: Comments (Atom)

Popular Posts

  • Applying Computer System Security (GAMP)
    It is a regulatory requirement that access to computerised systems is limited to authorised users. This not only limited to systems that con...
  • Deleting Electronic Data
    Hybrid Systems (Deleting Electronic Data) In Hybrid systems the computerised system is used to generate a record which is printed and hand s...
  • CSV FDA Warning Letter : Periodic Review
    Date: 21 May 2010 Link: FDA Warning Letter (New Window) Observation6. Your firm failed to check the accuracy of the input to and output from...
  • FDA Announce Part 21 CFR 11 Inspections
    Image via WikipediaAs detailed within the post 21 CFR Part 11 Warning Letters the FDA are planning to start conducting part 11 inspections s...
  • Spreadsheet Validation
    Spreadsheets have become commonly used within a wide range of applications within the pharmaceutical and biotechnology industries. These ran...
  • Software Validation
    The validation of computer software within the Pharmaceutical Industry is providing documented evidence that the software and computer syste...
  • CSV Periodic Review
    Regulatory requirement Both the FDA and EU GMP’s detail the requirement for demonstrating that a computer system remains in a validated stat...
  • CSV FDA Warning Letters : Laboratory Systems Security
    Date: 20 April 2010 Link: FDA Warning Letter (New Window) ObservationThis is a follow up letter from an inspection in 2009 where the securit...
  • Risk Management – A Continuous Process
    Introduction As discussed in previous posts the regulatory expectation is that risk management will be applied to all lifecycle phases of a ...
  • FDA Warning Letter - Alarm Management
    Date: 25 May 11 Link FDA 483 (PDF - New Window) Observation b. During routine operations, if there is an alarm event (e.g., time out, high a...

Categories

  • 21 CFR Part 11
  • ASTM-2500
  • Electronic Records
  • EU Annex 11
  • FDA News
  • FDA Warning Letters
  • GAMP 5
  • MHRA
  • Quality Assurance
  • Quality Risk Management
  • Spreadsheets
  • Supplier Audit
  • Testing
  • Validation

Blog Archive

  • ▼  2012 (6)
    • ►  November (1)
    • ►  August (1)
    • ►  July (1)
    • ►  April (1)
    • ►  February (1)
    • ▼  January (1)
      • Definition of Raw Data
  • ►  2011 (14)
    • ►  December (2)
    • ►  September (1)
    • ►  May (1)
    • ►  April (3)
    • ►  March (3)
    • ►  February (4)
  • ►  2010 (26)
    • ►  December (2)
    • ►  August (1)
    • ►  July (2)
    • ►  June (7)
    • ►  May (14)
Powered by Blogger.

About Me

Unknown
View my complete profile