3 hours ago · The FDA defines drug compounding as a practice in which a licensed pharmacist, physician or individual under the supervision of a licensed pharmacist modifies the ingredients of a drug to create
Human Medications, Human Drugs, Animal Medications, Animal Drugs, Pharmacy law, Pharmaceutical law, Compounding law, Sterile and Non Sterile Compounding 797 Compliance, Veterinary law, Veterinary Compounding Law; Health Care; Awareness of all Types of Compounding Issues; Pharmacy Benefit Managers (PBMs), Outsourcing Facilities Food and Drug Administration and Compliance Issues
Tuesday, April 24, 2018
| 04/18/2018 | Phase 4 Pharmaceutical LLC | Dallas District Office | CGMP/Finished Pharmaceuticals/Adulterated | Not Issued * |
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