Code of Federal Regulations · Subpart

Subpart B — Procedures For Domestic Blood Product Establishments

21 C.F.R. pt. 607, subpt. B

• § 607.20 Who Must Register And Submit A Blood Product List
• § 607.21 Times For Establishment Registration And Blood Product Listing
• § 607.22 How To Register Establishments And List Blood Products
• § 607.25 Information Required For Establishment Registration And Blood Product Listing
• § 607.26 Amendments To Establishment Registration
• § 607.30 Updating Blood Product Listing Information
• § 607.31 Additional Blood Product Listing Information
• § 607.35 Blood Product Establishment Registration Number
• § 607.37 Public Disclosure Of Establishment Registration And Blood Product Listing Information
• § 607.39 Misbranding By Reference To Establishment Registration, Validation Of Registration, Or To Registration Number