SECTIONS & SUB-SECTIONS TITLE RATIONALE TIMELINES COMPLETED

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2 Model Standards for Pharmacy Compounding of Non-Hazardous Sterile Preparations Schedule of Implementation (Note: New Sterile Compounding Sites are expected to be compliant immediately with all Model Standards requirements) SECTIONS & SUB-SECTIONS TITLE RATIONALE TIMELINES COMPLETED INTRODUCTION OBJECTIVES REGULATORY FRAMEWORK Needs to become familiar with the framework 4 ABBREVIATIONS 5 CORE REQUIREMENTS FOR A STERILE COMPOUNDING SERVICE Personnel needs to understand their role and responsibilities 5.1 Personnel Roles and responsibilities Pharmacy manager or pharmacy department head Sterile compounding supervisor Compounding personnel Training and assessment All personnel Conditions Initial training and assessment program Competency assessment program Management of the competency assessment program involved will have received training 5.2 POLICIES AND PROCEDURES Policies and procedures need to be prepared and made available to all personnel for training Within 6 months for the establishment of the competency program Within 6 months full implementation Model Standards for Pharmacy Compounding of Non-Hazardous Sterile Preparations Schedule of Implementation New Brunswick College of Pharmacists 1

3 5.3 FACILITIES AND EQUIPMENT Developmental and planning begin immediately. Longer period for allowing acquisition of equipment. and if there are changes/upgrades required an action plan must be prepared to show a full implementation within a 2-year frame Useful references To become familiar immediately with references ISO Standard To become familiar immediately with references Facilities reserved for the compounding of non-hazardous sterile preparations Developmental and planning begin immediately. Longer period for Dimensions Lighting Heating, ventilation and air conditioning systems for controlled rooms (clean room and anteroom) allowing acquisition Windows and openings of equipment Compounding areas Shared facilities All other facilities Materials and finishes Accessories Work surfaces and furniture Signage Facility Maintenance Equipment Required for sterile compounding Primary Engineering Control Required for sterile compounding and if there are changes/upgrades required an action plan must be prepared to show a full implementation within a 2-year frame Model Standards for Pharmacy Compounding of Non-Hazardous Sterile Preparations Schedule of Implementation New Brunswick College of Pharmacists 2

4 Other devices, instruments or accessories related to the compounding of non- Required for sterile hazardous sterile preparations compounding Personal protective equipment and clothing Personnel needs to be appropriately garbed and gloved Cleaning and disinfecting in areas reserved for the compounding of non-hazardous Cleaning and sterile preparations disinfection need to General be appropriately Disinfectant performed Equipment used for cleaning and disinfection and its storage Garbing of cleaning and disinfecting personnel (housekeeping personnel) Cleaning frequency 5.4 GENERAL MAINTENANCE LOG 6 PRODUCT AND PREPARATION REQUIREMENTS BUD established in accordance with Model Standards requirements 6.1 Beyond-use date and dating methods Beyond-use date for preparations Beyond-use dates for commercially available products according to type of container (single-dose vial or multiple-dose container) Single-dose vial Open ampoule Multi-dose container (ex. Vials) Beyond-use date according to risk of microbial contamination Beyond-use dates for immediate-use preparations Beyond-use dates of 12 hours or less for preparations compounded in segregated 6.2 Compounded sterile preparation protocols Documentation needs to be in line with Model Standards requirements 6.3 Compounded sterile preparation log Documentation Compounded sterile preparation log for one patient (individual preparations) Compounded sterile preparation log for preparations prepared in batches needs to be in line with Model Standards Full implementation within 6 months and if there are changes/upgrades required an action plan must be prepared to show a full implementation within a 2-year frame Within 6 months Within 6 months Model Standards for Pharmacy Compounding of Non-Hazardous Sterile Preparations Schedule of Implementation New Brunswick College of Pharmacists 3

5 requirements 6.4 Patient file 6.5 Conduct of personnel in areas reserved for the compounding of sterile preparations Personnel will have appropriate Conditions that may affect preparation quality conduct Conduct before entering the anteroom Conduct in controlled areas (clean room and anteroom) 6.6 Aseptic compounding of non-hazardous sterile preparations Adherence to General Hand and forearm hygiene and garbing Hand and forearm hygiene Garbing Introducing products and equipment into the clean room Cleaning and disinfecting the primary engineering control (PEC) Aseptic technique for compounding sterile preparations Verification of final compounded sterile preparations Role of personnel in verification Process for verification Verification by image capture or live camera Verification not required Second verification Labelling of final compounded sterile preparations General Label and insert aseptic technique is essential 6.7 Packaging Within 6 months Packaging process Packaging procedure 6.8 Storage Within 6 months 6.9 Transport and delivery of compounded sterile preparations Within 6 months 6.10 Recall of sterile products or final compounded sterile preparation Within 6 months 6.11 Incident and accident management Within 6 months Model Standards for Pharmacy Compounding of Non-Hazardous Sterile Preparations Schedule of Implementation New Brunswick College of Pharmacists 4

6 6.12 Waste management Within 6 months 7 QUALITY ASSURANCE PROGRAM A longer period with 7.1 Program content may be required to full implementation 7.2 Results and action levels develop and in a 2-year period 7.3 Verification of equipment and facilities implement appropriate Verification of equipment supporting compounding activities program Certification Temperature readings Verification of controlled rooms and the primary engineering control (PEC) Certification Certificate provided by manufacturer (in factory) Environmental verification 7.4 Quality assurance of personnel involved in aseptic compounding Gloved fingertip sampling (GFS) Media fill test 7.5 Quality assurance of compounded sterile preparations Within 6 months 7.6 Documentation of quality control activities Within 6 months 8 SOURCE FOR ADDITIONAL INFORMATION 9 GLOSSARY 10 LIST OF TABLES 11 APPENDICES POLICIES AND PROCEDURES FOR THE COMPOUNDING OF NON-HAZARDOUS 1 2 STERILE PREPARATIONS MANDATORY AND SUPPLEMENTAL REFERENCES Model Standards for Pharmacy Compounding of Non-Hazardous Sterile Preparations Schedule of Implementation New Brunswick College of Pharmacists 5

7 3 TRAINING OF COMPOUNDING PERSONNEL AND CLEANING AND DISINFECTING PERSONNEL PROCEDURE TEMPLATE 4 MINIMUM INDICATORS FOR CERTIFICATION OF CONTROLLED AREAS AND 5 PRIMARY ENGINEERING CONTROL CERTIFICATION OF CONTROLLED AREAS, LAMINAR AIRFLOW WORKBENCHES AND 6 BIOLOGICAL SAFETY CABINETS TEMPLATE FOR THE DRAFTING OF COMPOUNDING PROTOCOLS TO BE 7 COMPLETED FOR EACH DRUG EXAMPLES OF STERILE PREPARATIONS THAT MUST BE VERIFIED AT EACH STAGE OF 8 COMPOUNDING EXAMPLES OF STERILE PREPARATIONS THAT DO NOT REQUIRE VERIFICATION 9 DURING THE COMPOUNDING PROCESS TEMPERATURES FOR DIFFERENT TYPES OF STORAGE 10 INCIDENT/ACCIDENT REPORTING AND FOLLOW-UP FORM 11 COMPONENTS OF A QUALITY ASSURANCE PROGRAM BIBLIOGRAPHY Model Standards for Pharmacy Compounding of Non-Hazardous Sterile Preparations Schedule of Implementation New Brunswick College of Pharmacists 6

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