FDA GMP 111 Dietary Supplements

Hi Everyone,

I need your help about the interpretation of the following points about the GMP parte 111 on dietary supplements:

1. Sec. 111.70 c (1) : does the company has to demonstrate through a validation the in-process specification?
2. Sec. 111.80: does the company need to collect and hold all the lot code of the dietary ingredients, packaging and label. Do I need to verify each incoming of dietary ingredients?

Thanks you very much for your collaboration in advance,

Best regards