The Compounding Quality Act (CQA) amends the U.S. Food, Drug & Cosmetic Act (Act) to create a new, voluntary category of compounders called "outsourcing facilities" (OF). Compounded drugs are those mixed by a pharmacist that differ from commercially available drugs according to individual needs. If a pharmacy chooses to register as an OF, it will be exempt from the new drug application, labeling, and track and trace requirements imposed on pharmaceutical manufacturers. In addition, the OF will be permitted to dispense drugs without an individual patient prescription.
In order to register as an OF, the facility must do the following:
- Compound by or under the direct supervision of a licensed pharmacist;
- Pay a $15,000 annual fee (small business fee TBD);
- Register annually with FDA;
- Report to FDA every June and December:
- what drugs have been compounded in the facility in the prior 6 months
- adverse events;
- Allow FDA inspections
- on a risk-based frequency schedule, depending on prior safety performance
- additional fees to be assessed if reinspection is necessary.
OFs are prohibited from:
- Compounding from any bulk substance that does not appear on a list of APIs deemed permissible by FDA;
- Compounding any drugs that appear on a list of drugs deemed by FDA to be demonstrably difficult to compound;
- Reselling a compounded drug;
- Intentionally falsifying a prescription for a compounded drug.
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