Phase 1 (Pre-Visit)

A guided walkthrough on preparatory work required by the pharmacy, including consolidating and preparing all documents to be evaluated (e.g., Policies & Procedures, Master Formulation Records), completion of a questionnaire to better understand the pharmacy's specific practice, providing cleaning and compounding schedules so the consultant can work around the pharmacy schedule, and preparation for the Garbing and Gloved Fingertip and Thumb Sampling and Media-Fill Test to assess aseptic technique.

Phase 2 (Visit)

Pharmacy-tailored, onsite visit with the consultant for an a-z appraisal of the sterile compounding supervisors theoretical and practical competencies based on NAPRA Model Standards implemented as per provincial/territorial regulatory authorities, including their ability to apply and oversee aseptic technique compounding and cleaning & disinfecting personnel training programs, written policies & procedures, facility engineering and environmental control management program, risk management protocols, MFR and CR database, among more.

Phase 3 (Post-Visit)

A comprehensive written sterile compounding supervisor's third-party evaluation, including findings and observations on conformance, competency, and compliance in their roles and responsibilities to meet NAPRA requirements for non-HD and HD sterile compounding supervision as implemented by NAPRA.

Consultant travel and accommodations not included.