2006D-0383 | Characterization and Qualification of Cell Substrates and Other Biological Starting Materials Used in the Production of Viral Vaccines for the Prevention and Treatment of Infectious Diseases | |||||||||||||||||||||||
FDA Comment Number : | EC3342 | |||||||||||||||||||||||
Submitter : | Mrs. Tricia Harrod | Date & Time: | 12/15/2006 08:12:48 | |||||||||||||||||||||
Organization : | Mrs. Tricia Harrod | |||||||||||||||||||||||
Category : | Health Professional | |||||||||||||||||||||||
Issue Areas/Comments | ||||||||||||||||||||||||
GENERAL | ||||||||||||||||||||||||
GENERAL | ||||||||||||||||||||||||
I am writing to ask you to issue guidelines to pharmacceutical companies that when manufacturing vaccines they restrict their use of stem cells to those lines established from sources other than fetal tissue obtained from aborted babies.
It only makes sense to utilize non-objectionable cell lines in vaccine production so that all people can benefit from them without compromising their moral beliefs and pro-life convictions. This is especially true since there is an abundance of ethical sources. Sincerely, Tricia K Harrod Aberdeen, SD | ||||||||||||||||||||||||