StacksVerified U.S. regulatory reference

Part 606 — Current Good Manufacturing Practice for Blood and Blood Components

Subpart A — General Provisions

Subpart B — Organization and Personnel

Subpart C — Plant and Facilities

Subpart D — Equipment

Subpart F — Production and Process Controls

Subpart G — Additional Labeling Standards for Blood and Blood Components

Subpart H — Laboratory Controls

Subpart I — Records and Reports