Records as per Section 7.1,d - What records is section 7.1d talking about?
I got asked this question - What records is section 7.1d talking about?
I said that it meant "records the company requires to be generated in the product realisation chain" which are in addition to those records which the standard requires us to keep.
That is right isn’t it?
If the placebo effect is so effective why is it not used as a legitimate treatment?