For the new year i have been asked to put in place a schedule of GMP audits. Well, that's not strictly true, the management team have been asked and they have politely tried to slide it over onto my desk
( I am an external technical support, I do Internal audits, Hygiene/fabrication/equipment audits monthly and generally keep the documentation around BRC certification up to date and in control).
Now, I believe that GMP audits are a tool for showing personnel on site the things that appear day-to-day in a facility, and are not just for the purpose of generating long lists of non-conformances, which I do anyway on a monthly basis.
Can you guys give me some pointers on how you deal with GMP audits, frequency, format, and scope. I have a meeting on Monday and I hope to have some cool ideas to pour forth!
Thanks and HAPPY NEW YEAR to all here and all the IFSQN Team