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Regulatory guidelines by Medicines and Healthcare products Regulatory Agency- UK MHRA including GMP - Orange Guide, Good Manufacturing Practice Updates.Good Documentation Practices. Documentation Requirements For Regulated Environments There was no awareness that the records for good practice. This document provides guidance for the interpretation of the principles and guidelines of good manufacturing practice (GMP) for medicinal products as laid The Medicines and Healthcare products Regulatory Agency (MHRA) carries out inspections to check if manufacturing and distribution sites comply with GMP or GDP. Good Documentation Practices, commonly referred to as GDPs, are the guidelines that one follows in recording raw data entries in a legible, traceable and In the context of these guidelines, good documentation practices are those measures that collectively and individually ensure documentation, whether paper or