SUBPART D—Records and Reports (§310.303 to §310.305) - Title 21 - Food and Drugs CFR - USA Laws Searching

CFR > Title 21 - Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER D—DRUGS FOR HUMAN USE (parts 300 to 370) > PART 310—NEW DRUGS > SUBPART D—Records and Reports (§310.303 to §310.305)

SUBPART D—Records and Reports (§310.303 to §310.305)

310.303—Continuation of long-term studies, records, and reports on certain drugs for which new drug applications have been approved.
310.305—Records and reports concerning adverse drug experiences on marketed prescription drugs for human use without approved new drug applications.