Pharmacy · Regulatory Affairs
In the context of regulatory submissions, 'Type III' of a Drug Master File (DMF) provides information about which of the following?
- 1Excipients, colorants, flavors, essences, or materials used in their preparation
- 2Packaging materials✓
- 3Facilities, personnel, operating procedures, and drug product manufacturing
- 4Drug substances, drug substance intermediates, and materials used in their preparation
Correct answer
Packaging materials
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