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Compounding 2016: What's New, What's Not (Summerville Regional)


Summerville Regional
295 Midland Pkwy, Cafeteria Classrooms
Summerville, SC  29485
 
Date:        April 14, 2016
Time:      4:00pm-6:00pm
 
Target Audience: This training is intended for pharmacists and pharmacy technicians who work with sterile products and hazardous medication compounding.
 
Learning objectives for the the pharmacist and pharmacy technician:
* List requirements of current USP Chapter <797>, the newly published Chapter <800>, and sections of USP
Chapter <795> relevant to institutional practice.
* Review implementation timelines from regulatory agencies for enforcement of new or proposed requirements
from USP or FDA.
* Review hazardous drug handling, storage, administration and disposal laws and best practices from USP <800.
* Compare current state and federal law vs current guidelines vs best practice regarding sterile, non-sterile, and
hazardous compounding.
* Describe tools and methods to drive compliance with safety and legal requirements in sterile, non-sterile and
hazardous compounding
* Discuss examples of sterile compounding errors or contamination

 

Date: Apr 14, 2016 04:00 PM - 06:00 PM

Fee

$35.00

CE Hours

2.00

CE Units

0.200

Activity Type

  • Knowledge

Target Audience(s)

  • Pharmacists
  • Pharmacy Technicians

Accreditation(s)

Accreditation Council for Pharmacy Education
The University of South Carolina College of Pharmacy is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.

Requirements for CE Credit

Participants must sign in at the beginning of the program, attend the entire session, successfully complete the post-test, and complete the on-line evaluation within 30 days of the live event. Participants must update their NABP e-profile to allow reporting to the CPE monitor. No partial credit will be awarded. 
 
 
 

 

 

 

   

At the completion of this activity, the participant will be able to:
* List requirements of current USP Chapter <797>, the newly published Chapter <800>, and sections of USP
Chapter <795> relevant to institutional practice.
* Review implementation timelines from regulatory agencies for enforcement of new or proposed requirements
from USP or FDA.
* Review hazardous drug handling, storage, administration and disposal laws and best practices from USP <800.
* Compare current state and federal law vs current guidelines vs best practice regarding sterile, non-sterile, and
hazardous compounding.
* Describe tools and methods to drive compliance with safety and legal requirements in sterile, non-sterile and
hazardous compounding
* Discuss examples of sterile compounding errors or contamination

Speaker(s)/Author(s)

Carole Small Russell, RPh, MHSA
Compounding Pharmacist, MUSC

Activity Number

0062-9999-16-067-L03-P/T
Date: 04/14/16
Time: 04:00 PM - 06:00 PM

CE Hours

2.00