Question

According to Company Policy, which items are required

to be kept in the pharmacy's Nonsterile Compounding
Binder?

Answer 1

In the pharmacy's Nonsterile Compounding Binder, the required items include glass slides, laboratory metric rulers, Kimwipes, sterile swabs, sterile wood applicator sticks, and a stock of laboratory supplies.

Step-by-step explanation:

The items that are required to be kept in the pharmacy's Nonsterile Compounding Binder, according to Company Policy, include glass slides, clear plastic flexible laboratory metric rulers, Kimwipes and/or lens paper, sterile 10 ml glass pipettes, sterile swabs, sterile wood applicator sticks, and a maintained stock of laboratory supplies. These items are necessary for nonsterile compounding procedures in the pharmacy.

Answer 2

According to company policy, the Nonsterile Compounding Binder should contain all necessary documentation and procedures related to the preparation and handling of nonsterile compounded medications. The specific items that should be included in the binder may vary depending on the policies of the individual pharmacy and the regulatory requirements in the jurisdiction in which the pharmacy is located.

In general, the Nonsterile Compounding Binder should contain the following items:

Standard Operating Procedures (SOPs) for the preparation and handling of nonsterile compounded medications, including guidelines for handling hazardous materials and ensuring the safety of patients and staff.

Documentation of training and competency assessments for pharmacy staff who are involved in the compounding of nonsterile medications.

A log of all nonsterile compounded medications prepared, including the date, time, and quantity of each preparation.

Quality control records for nonsterile compounded medications, including documentation of testing and stability studies.

Written policies and procedures for the storage, handling, and disposal of nonsterile compounded medications.

Any relevant regulatory documents, such as pharmacy licenses and accreditation documents.

Any other documentation or procedures that are required by company policy or regulatory agencies.