21 CFR § 600.15 Biological Products: General

§ 600.15 Temperatures during shipment.

Current through Sep 8, 2026 · Read all of Part 600

⚠ 2 pending changes to Part 600

The following products shall be maintained during shipment at the specified temperatures:

(a) Products.

ProductTemperature
Cryoprecipitated AHF−18 °C or colder.
Measles and Rubella Virus Vaccine Live10 °C or colder.
Measles Live and Smallpox VaccineDo.
Measles, Mumps, and Rubella Virus Vaccine LiveDo.
Measles and Mumps Virus Vaccine LiveDo.
Measles Virus Vaccine LiveDo.
Mumps Virus Vaccine LiveDo.
Fresh Frozen Plasma−18 °C or colder.
Liquid Plasma1 to 10 °C.
Plasma−18 °C or colder.
Platelet Rich PlasmaBetween 1 and 10 °C if the label indicates storage between 1 and 6 °C, or all reasonable methods to maintain the temperature as close as possible to a range between 20 and 24 °C, if the label indicates storage between 20 and 24 °C.
PlateletsBetween 1 and 10 °C if the label indicates storage between 1 and 6 °C, or all reasonable methods to maintain the temperature as close as possible to a range between 20 to 24 °C, if the label indicates storage between 20 and 24 °C.
Poliovirus Vaccine Live Oral Trivalent0 °C or colder.
Poliovirus Vaccine Live Oral Type IDo.
Poliovirus Vaccine Live Oral Type IIDo.
Poliovirus Vaccine Live Oral Type IIIDo.
Red Blood Cells (liquid product)Between 1 and 10 °C.
Red Blood Cells Frozen−65 °C or colder.
Rubella and Mumps Virus Vaccine Live10 °C or colder.
Rubella Virus Vaccine LiveDo.
Smallpox Vaccine (Liquid Product)0 °C or colder.
Source Plasma−5 °C or colder.
Source Plasma Liquid10 °C or colder.
Whole BloodBlood that is transported from the collecting facility to the processing facility shall be transported in an environment capable of continuously cooling the blood toward a temperature range of 1 to 10 °C, or at a temperature as close as possible to 20 to 24 °C for a period not to exceed 6 hours. Blood transported from the storage facility shall be placed in an appropriate environment to maintain a temperature range between 1 to 10 °C during shipment.
Yellow Fever Vaccine0 °C or colder.

(b) Exemptions. Exemptions or modifications shall be made only upon written approval, in the form of a supplement to the biologics license application, approved by the Director, Center for Biologics Evaluation and Research.

[39 FR 39872, Nov. 12, 1974, as amended at 49 FR 23833, June 8, 1984; 50 FR 4133, Jan. 29, 1985; 50 FR 9000, Mar. 6, 1985; 55 FR 11013, Mar. 26, 1990; 59 FR 49351, Sept. 28, 1994; 64 FR 56449, Oct. 20, 1999]

← § 600.14 Reporting of biological product deviations by licensed manufacturers.§ 600.20 Inspectors. →