Components of the checklist:
These checklists are a composite of bullet points from (1) regulations, (2) guidance documents, and (3) apheresis device manufacturer directions/specifications that have been a useful reference to the minimum requirements that should be contained in apheresis submissions. The checklists are living documents that undergo regular revision as the source materials change. They do not constitute current or future review policy. Note that the device manufacturer directions/specifications are also subject to change at any time and the latest versions from the manufacturer should always be consulted.
- Apheresis RBC Review Checklist: General represents bullet points from "Guidance for Industry: Recommendations for Collecting Red Blood Cells by Automated Apheresis Methods", February 2001.
- Leukocyte Reduction Review Checklist: General represents bullet points from "Recommendations and Licensure Requirements for Leukocyte-Reduced Blood Products", May 29, 1996.
- Platelet Pheresis Review Checklist: General represents bullet points from "Revised Guideline for the Collection of Platelets, Pheresis", October 7, 1988.
- Infrequent Plasma Donors Checklist: General represents bullet points from "Revision of FDA Memoradum of August 27, 1982: Requirements for Infrequent Plasma Donors", May 10, 1995.
- SOPs and Labeling: represents bullet points for required documents to submit
- QC sheets: represents regulatory requirements for records and documentation
- As of the date of the document, each device manufacturers directions/specifications for:
- Baxter ALYX
- Haemonetics MCS Plus LN 8150
- Haemonetics MCS Plus LN 9000
- Trima Version 5.1 (should also apply to version 4 and above except where noted)
- Amicus (Baxter)