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Re: Buffalobob2199 post# 8085

Friday, 12/29/2017 11:55:23 AM

Friday, December 29, 2017 11:55:23 AM

Post# of 10354
GMP - good manufacturing practice

The drug mfr (sub contractor co selected by ARTH) has to submit all details to fda to certify the mfg and processes to mfr the product.

CEB was typo - it is CE mark application in Europe

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