What minimum requirements must be included in the policy and procedure manual for sterile product quality assurance under Ohio law?

In Ohio, the regulations surrounding the compounding of sterile products necessitate specific elements to be included in the policy and procedure manual that ensures quality assurance. Choosing an option that recognizes the inclusion of two critical components reflects an understanding of these requirements.

One essential aspect is the need for a quality assurance program tailored for both personnel and product monitoring. This component ensures that the staff involved in compounding sterile products is adequately trained and that products are consistently evaluated for quality and safety, which are fundamental in maintaining compliance with practice standards.

Additionally, having a current manual available for inspection is crucial in fostering transparency and accountability. This allows for oversight by regulatory bodies and ensures that all procedures are documented and accessible for review. It demonstrates the pharmacy's commitment to adhering to established guidelines and facilitates compliance with state and federal regulations.

By selecting the option that signifies the importance of including these elements in the policy and procedure manual, the answer highlights a balanced approach to quality assurance encompassing personnel training and procedural availability for scrutiny, both of which are pivotal in the realm of sterile product compounding in Ohio.