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USP Chapter <795> focuses on nonsterile compounding, with updates aimed at improving quality, safety, and consistency. These voluntary standards provide clear guidelines on personnel, equipment, training, and documentation, ensuring that patients receive medications that are safe and free from contaminants.
The following blog is written by Epicur Pharma’s Advisory Council member Jan Woods, a veterinary hospital consultant, and national speaker with expertise in DEA compliance, state and federal regulations, and clinic and hospital practice management. If so, did you document it? Mistakes happen – bottles spill or break.
Some of the biggest changes that GFI #256 brings include: Increased documentation for patient-specific prescriptions Limitations to available 503A office-stock drugs Although veterinary professionals were aware of the impending changes with GFI for months, many have been left scrambling since it went into effect in April. Read our blog!
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