· CROSS-CUTTING
GDocP

Good Documentation Practice

ALCOA+ data integrity and record governance.

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WHAT IT GOVERNS

Good Documentation Practice governs how GxP records and data are created, reviewed, corrected, stored, and retained — the ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, plus Complete, Consistent, Enduring, and Available) applied across both paper and electronic systems. It is the data-integrity discipline underneath every other GxP record.

WHY IT MATTERS

Data integrity is the foundation every other control rests on: in a GxP world, if it isn’t documented, it didn’t happen — and if the documentation can’t be trusted, none of the quality claims built on it can be either. Data-integrity failures (backdating, shared logins, deleted results, uncontrolled audit trails) are among the most severe findings a regulator can issue, up to import alerts and consent decrees.

KEY FOCUS AREAS
01

The ALCOA+ principles

Records that are attributable, legible, contemporaneous, original, and accurate — plus complete, consistent, enduring, and available — as the working definition of trustworthy data.

02

Contemporaneous recording & review

Recording at the time of the activity and independent second-person review, so entries are neither reconstructed after the fact nor self-certified.

03

Audit trails & electronic records

Secure, time-stamped audit trails that capture who did what and when, reviewed as part of the record — the electronic equivalent of an uncorrected logbook.

04

Record retention & archival

Controlled retention, protection from alteration or loss, and retrievability for the full required lifetime of the record.

STANDARDS SPEQ DECODES · 3
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MHRA GxP DI (2018)MHRAHIGH INSPECTION RISK
MHRA 'GxP' Data Integrity Guidance and Definitions
PIC/S PI 041-1PIC/SHIGH INSPECTION RISK
Good Practices for Data Management and Integrity in Regulated GMP/GDP Environments
21 CFR Part 1304DEA
Records and Reports of Registrants
WHAT INSPECTORS LOOK AT
  • Audit-trail review — is it enabled, complete, and actually reviewed?
  • Contemporaneousness of entries and how corrections are made and justified
  • Access controls, unique logins, and segregation of duties
  • Data governance policy and the lifecycle of both paper and electronic records
KEY REGULATORY BODIES
MHRAPIC/SDEA

Derived from the 3 standards SPEQ decodes for this discipline.

RELATED DISCIPLINES
CSVComputerised System ValidationGMPGood Manufacturing PracticeQMSQuality Management Systems
THE FRAMEWORK
How SPEQ maps this discipline across the three layers →
FDA QMM
The maturity of the quality system behind this discipline →
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