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


Trident Regional
9330 Medical Plaza, Cafe B                
Charleston, SC  29406
 
Date:           April 6, 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 6, 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. 
 
 
 

 

Wed, Apr 06, 2016
 

Compounding 2016: What's New, What's Not
   

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: 04/06/16
Time: 04:00 PM - 06:00 PM

CE Hours

2.00