Drug Safety Enhancement Act of 2011

[AI summary unavailable — showing source text] Drug Safety Enhancement Act of 2011 - Amends the Federal Food, Drug, and Cosmetic Act (FFDCA) to expand drug establishment registration requirements to include foreign drug establishments and establishments manufacturing, preparing, propagating, compounding, or processing excipients of drugs (i.e., inactive drug additives). Requires the Secretary of Health and Human Services (HHS) to collect registration fees. Requires drug manufacturers to: (1) implement an effective quality system that requires compliance with current good manufacturing practices and timely communication of product quality issues; (2) establish risk management procedures that ensure effective risk assessment, control, and communication; and (3) establish procedures that ensure the safety, identity, quality, strength, purity, and security of all drugs and other materials used by the manufacturer. Requires drug establishments to maintain records on the supply chain of the drug, ingredients, and raw materials. Establishes the frequency of inspections of drug establishments. Prohibits delaying or limiting an inspection. Gives the Secretary authority to order the recall of, detain, destroy, and seize drugs as necessar…