[Code of Federal Regulations]

[Title 21, Volume 1]

[Revised as of April 1, 2007]

From the U.S. Government Printing Office via GPO Access

[CITE: 21CFR50.50]

[Page 288]

TITLE 21--FOOD AND DRUGS

CHAPTER I--FOOD AND DRUG ADMINISTRATION,

DEPARTMENT OF HEALTH AND HUMAN SERVICES

PART 50_PROTECTION OF HUMAN SUBJECTS--Table of Contents

Subpart D_Additional Safeguards for Children in Clinical Investigations

Sec. 50.50 IRB duties.

Source: 66 FR 20598, Apr. 24, 2001, unless otherwise noted.

In addition to other responsibilities assigned to IRBs under this

part and part 56 of this chapter, each IRB must review clinical

investigations involving children as subjects covered by this subpart D

and approve only those clinical investigations that satisfy the criteria

described in Sec. 50.51, Sec. 50.52, or Sec. 50.53 and the conditions

of all other applicable sections of this subpart D.

http://a257.g.akamaitech.net/7/257/2422/26mar20071500/edocket.access.

gpo.gov/cfr_2007/aprqtr/21cfr50.50.htm

Testing on little innocent children is absolutely allowable. Just like any privacy policy or modern day contract, all rules will be followed by us to the letter, until we feel like changing them without notice to go ahead and do whatever we want in the name of research to benefit the future of mankind. Rabid monkey ebola? No problem, we'll do that too. Hey, it's science man. Shut up.

Say, got any kids you don't want?