Sterile Compounding Supervisor Third-Party Evaluation
A comprehensive one-on-one consultation package assisting you in meeting NAPRA's model standards for a sterile compounding supervisor third-party evaluations as adopted by provincial/territorial regulatory authorities.
"The sterile compounding supervisor must be evaluated For knowledge And abilities, at the same frequency As compounding personnel, by a third party (an evaluator With expertise In sterile preparation compounding, at arm's length from the facility/pharmacy and free of any real or perceived conflict with the individual being evaluated)."
NAPRA Model Standards for Pharmacy Compounding of Non-Hazardous and Hazardous Sterile Preparations
Segmented into 3 phases that allow a comprehensive and pharmacy-tailored approach.
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.
Content is currently not available in French. French version will be available soon.