What should pharmacy technicians refer to when selecting repackaging materials?

When selecting repackaging materials, referring to USP standards is essential because these standards provide guidance on the quality and safety of handling and repackaging pharmaceutical products. The United States Pharmacopeia (USP) sets forth specifications for the integrity, stability, and sterility of repackaged medications, ensuring that the materials used do not compromise the efficacy or safety of the drugs.

USP standards outline the criteria for various aspects, such as the type of containers and closures that should be used, the labeling requirements, and best practices for preventing contamination during the repackaging process. This ensures that pharmacy technicians adhere to the highest quality control measures and regulatory expectations.

While pharmaceutical regulations, manufacturer guidelines, and store policies are also important, they may not always provide the specific, technical detail needed for selecting materials in the context of repackaging. The USP standards encompass widely accepted practices that are crucial for maintaining the integrity of the medication being repackaged, which is why they are the most pertinent source in this situation.