1. 21 CFR, 5. FDA organization. Code of Federal Registrar.
2. 21CFR 211.65. Equipment construction. Code of Federal Registrar.
3. 21CFR 310.305. Records and reports concerning adverse drug experiences on marketed prescription drugs for human use without approved new drug applications. Code of Federal Registrar.
4. 21CFR 312.32. IND safety reports. Code of Federal Registrar.
5. 21CFR 314.80. Post marketing reporting of adverse drug experiences. Code of Federal Registrar.