The Pharmaceutical Manufacturing Standards Project has now moved to the ‘validation’ stage, which means final draft qualifications and units of competency are available for your validation and comment.
Validation means checking and confirming that the final drafts are logical and factually accurate. They have been re-written to incorporate the skills required to apply Good Manufacturing Practice (GMP) principles and procedures. We are seeking your views on whether the qualifications and units reflect the current skills standards and practices of industry, and whether job functions are accurately described. These final drafts will be available for validation and feedback until 1 February 2018. Please click the button below to be taken to the project webpage.
A summary of the feedback that was received during the consultation period (between 31 October – 7 December 2017) and a description of its consideration and application in these final drafts can be downloaded from the webpage.