Newnan, Georgia
Individuals attending the course in place of the registered individual will be honored as long as the request is made in advance of the registration deadline, which is 14 days prior to the start of the live component. Transfer participants must still complete the required pre-requisite self-study by the required cut-off date.
Refund requests are subject to a $200.00 cancellation fee and must be received 30 days prior to the start of the live component. All registration cancellations must be submitted in writing or by e-mail to the Continuing Education Department at the following address.
Continuing Education
Email: ce@SCCP.sc.edu
- Operating System: Windows XP SP2 or later, Windows Vista, Windows 7, Mac OS X 10.5 or later
- Internet Browser (Mac &/ Windows): Internet Explorer 7 or later, Firefox 3.5 or later, Safari 4
- Broadband Internet connection: Cable, High-speed DSL & any other medium that is internet accessible
- Peripherals: Computer speakers or headphones
- Monitor Screen Resolution: 320 x 480 or higher
- Media Viewing Requirements: For some components, the most up-to-date version of Adobe Flash may be required. To obtain the free Flash plug-in, go to http://get.adobe.com/flashplayer/.
Date: Oct 3, 2014 08:00 AM - Oct 4, 2014 05:15 PM
Fee
CE Hours
CE Units
Registration closes on Sep 18, 2014 11:59 PM
Activity Type
- Application
Target Audience(s)
- Pharmacists
- Pharmacy Technicians
Accreditation(s)
The University of South Carolina College of Pharmacy is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.
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Support/Credits
Time
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Session
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Format
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8:00-8:15am
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Registration, welcome, introductions
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8:15-10:15am
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Introduction to Sterile Compounding
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Lecture
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Overview of USP<797>
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Lecture
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10:15-10:30am
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Break
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10:30-noon
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Primary and Secondary Engineering Controls
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Lecture
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Particle Counter and Smoke Testing
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Lab/Demo
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12:00-12:45
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Lunch
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12:45-3:15pm
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Overview of supplies and equipment necessary for sterile compounding
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Lecture/Demo
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Hand hygiene, PPE, Garbing, Cleaning/Disinfecting hoods
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Lab
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3:15-3:30pm
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Break
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3:30-5:00pm
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Review of Relevant Calculations for Sterile Compounded Products
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Lecture/Lab
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5:00-5:30pm
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Review, discussion, observations
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Time
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Session
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Format
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8:00-10:15am
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Discussion of Low/Medium risk sterile compounding and aseptic technique
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Lecture
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Vial pressures, Labels and Compatibility/Stability
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Lecture/Demo/Lab
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10:15-10:30am
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Break
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10:30-11:45am
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Hands on training of Low/Medium risk sterile compounding and aseptic technique
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Lab
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11:45a-12:30p
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Lunch
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12:30-2:30pm
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Assessments of Student Skills in Low/Medium Risk Sterile Compounding and Aseptic Technique
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Lab
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2:30-2:45pm
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Break
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2:45-4:45pm
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Contamination, QA/QC for CSP
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Lecture
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Special Topics
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Lecture
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4:45-5:15pm
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Wrap up, Q&A, Remediation
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- Define parenteral preparations and the role of safety, accuracy and attitude in risk prevention
- Discuss United States Pharmacopeia chapters applicable to pharmaceutical compounding of sterile products
- Define the role of the pharmacist and the responsibilities pertaining to sterile compounding
- Describe supplies and equipment used in sterile compounding and the safety considerations
- Summarize the microbiological considerations in sterile compounding and the responsibilities of personnel in preventing contamination
- Classify sterile preparations as low-, medium- or high risks and determine appropriate BUDs
- Differentiate between primary and secondary engineering controls and the role they play in maintenance of sterile environment for sterile compounding
- Describe the critical steps in proper aseptic technique and compounding manipulations
- Distinguish between quality control and quality assurance for sterile compounding
- Identify the key areas for monitoring for environment, personnel and end-product testing for a sterile compounding program
- Define parenteral preparations and the role of safety, accuracy and attitude in risk prevention
- Discuss United States Pharmacopeia chapters applicable to pharmaceutical compounding of sterile products
- Define the role of the pharmacy technician and the responsibilities pertaining to sterile compounding
- Describe supplies and equipment used in sterile compounding and the safety considerations
- Summarize the microbiological considerations in sterile compounding and the responsibilities of personnel in preventing contamination
- Classify sterile preparations as low-, medium- or high risks preparation based on their ISO class
- Differentiate between primary and secondary engineering controls and the role they play in sterile compounding
- Describe the critical steps in proper aseptic technique and compounding manipulations
- Distinguish between quality control and quality assurance for sterile compounding
- Identify the key area for monitoring for environment, personnel and end-product testing for a sterile compounding program
- Chapter 1: Pages 1-15 and complete review questions on page 14-15
- Chapter 2: Pages 17-62 and complete review questions and case studies on page 62
- Chapter 4: Pages 107-135 and completer review questions and case study on pages 135-137.
- Chapter 5: Pages 141-171 and complete review questions and case study on pages 171-172. View required video for Chapter 5:
- on Page 148: Cleaning the HLFW (Video length 3:58)
- Chapter 6: Pages 175-220 and complete review questions and case studies on pages 220-222. View required videos for Chapter 6:
- Page 177: Hand Washing (Video length TBD)
- Page 181: Personal Protective Equipment -Garbing(Video length 0:44)
- Page 181: Personal Protective Equipment-Sterile Gloves (Video Length 1:16)
- Page 189: Attach Needle to Syringe and Remove Cap of Needle (Video Length 0:43)
- Page 190: Enter Vial (Video length 1:02)
- Page 192: Withdraw Contents-equal pressure Milking (Video length 0:53)
- Page 192: Withdraw Contents Reverse Milking(Video length 0:36)
- Page 197: Removal of Air Bubbles (Video length 0:54)
- Page 199: Ampule Breaking (Video length 0:59)
- Page 199: Using A filter needle (1:28)
- Page 199: Using a filter straw (1:31)
- Page 206: Reconstituting Medications for Parenteral Administration (Video length 2:15)
- Page 208: Uncapping and Recapping Needles (Video length 0:38)
- Page 209: Capping a Syringe (Video length 0:51)
- Page 210: Priming an Infusion Set (Video length TBD)
- Page 211: Positive Pressure (Video length 1:12)
- Page 212: Negative Pressure (Video length 0:50)
- Page 218: Workflow Process (Video length 2:12)
- Page 361: Gloved Fingertip Test (Video length 1:06)
Registration closes on Sep 18, 2014
at 11:59 PM
Registration Closed
Activity Number
0062-0000-14-094-H04-P/T
CE Hours
Registration Closed
Speaker(s)/Author(s)
Carole Small Russell, RPh, MHSA
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Kathy Quarles-Moore, B.S.Pharm, RPh, CDM
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Nancy Roberts, PharmD, MS
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Michaela Almgren, PharmD, MS
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