| 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 : | EC2411 | |||||||||||||||||||||||
| Submitter : | Mrs. Valerie Porter | Date & Time: | 12/01/2006 08:12:45 | |||||||||||||||||||||
| Organization : | Mrs. Valerie Porter | |||||||||||||||||||||||
| Category : | Drug Industry | |||||||||||||||||||||||
| Issue Areas/Comments | ||||||||||||||||||||||||
| GENERAL | ||||||||||||||||||||||||
| GENERAL | ||||||||||||||||||||||||
| There are a number of cell lines which have originated from ethical and completely non-controversial sources for the development of vaccines. I support the FDA recommending that pharmaceutical companies use these cells from non-controversial sources instead of cells derived from aborted children.
| ||||||||||||||||||||||||