RE: ECRw4 Aug 2022 15:44
I was VP of R&D in a major Pharma company before I retired. Requirements may be different in mining assay labs but it certainly wasn't simple or particularly quick to train and expand personnel and space to operate to what is called "Good Laboratory Practice" in our labs. It sounds very bland , I mean why wouldn't you operated to Good Practice as a matter of course? Well the devil is in the detail, detail running to thousands of pages, as required initially by the US FDA and then most regulatory authorities around the world. It requires everything from staff training records on every procedure they run, every detail about equipment usage eg equipment servicing, calibration, who did it when, which tests using it were run, by whom at what time and date etc and I could go on for ever. Absolutely everything has to be recorded as it happens, signed off as checked every day by the most senior scientist in the lab and records of everything done be simply auditable by the regulatory authorities. Bringing new people into that environment and training them in everything they need to know about compliance with the whole system beyond the actual hands on procedures they do day to day is not trivial.
But thats Phama, mining may be different but I suspect detailed procedures such as core sample traceability, systems security and record keeping will be JORC requirements.