USP requires water used in the manufacture of parenterals to be water for injection, WFI. Does Q7A conflict with this? 1.60K viewsOctober 10, 2022DrugsPharmaceutical 0 Sam Smith11.38K September 15, 2020 0 Comments Spread the loveSpread the love 1 Answer ActiveVotedNewestOldest 0 Blogolu28.38K Posted September 15, 2020 0 Comments Spread the loveNo. If you go back to the scope of Q7A, it clearly states that the sterilization and aseptic processing of sterile APIs are not covered by this guidance Spread the love You are viewing 1 out of 1 answers, click here to view all answers. Login
