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USP <800>: Understanding, Preparing, Implementing

Due to the overwhelming interest in this webinar on September 12th*, this webinar is being repeated:   

Tuesday, October 3, 2017, 2:00pm - 3:00pm CT
(3:00pm ET/1:00pm MT/12:00pm PT)

Register to attend ►

 

Description

With the implementation date of USP Chapter <800> fast approaching, pharmacies have little time left to ensure they become compliant with these newest regulations. This educational activity will help pharmacists and pharmacy technicians understand and prepare for these new standards. An overview of the risks of working with hazardous drugs and how ensuring compliance with USP <800> will mitigate these risks will be reviewed. This activity will also discuss strategies on how to implement and maintain compliance with USP <800>.

Learning Objectives

At the completion of this webinar, the participant will be able to:

  • Outline the hazardous drug regulatory standards of practice, including NIOSH, OSHA, State Boards of Pharmacy and USP <800>
  • Review containment engineering controls and their application
  • Describe facility design plans for non-sterile and sterile hazardous drug handling
  • Discuss supplemental engineering controls (i.e., closed system transfer devices)

Faculty

Fred Massoomi, Pharm.D., FASHP
Senior Director of Health-system & Hospital Services
Visante, Inc.
Omaha, Nebraska

Andrew Szkiladz, PharmD, BCPS, BCOP
Regional Oncology Pharmacy Manager
Baystate Health
Springfield, Massachusetts

Accreditation

*Note: If you attended this webinar on September 12, 2017 and received CE credit (i.e. a pharmacist or pharmacy technician CE statement of credit with ACPE UAN 0221-0000-17-378-L05-P/T), you will not be eligible to receive CE credit for the October 3 webinar.

Pharmacists and Pharmacy Technicians

ACPE LogoProCE, Inc. is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. ACPE Universal Activity Number 0221-0000-17-378-L05-P/T has been assigned to this live knowledge-based activity (initial release date September 12, 2017). This activity is approved for 1.0 contact hour (0.1 CEU) in states that recognize ACPE providers. The activity is provided at no cost to participants. Participants must complete the online post-test and activity evaluation to receive pharmacy CE credit. No partial credit will be given. Statements of completion will be issued online at www.ProCE.com, and proof of completion will be posted in NABP CPE Monitor profiles.

Disclosure

It is the policy of ProCE, Inc. to ensure balance, independence, objectivity and scientific rigor in all of its continuing education activities. Faculty must disclose to participants any significant financial interest or affiliation with companies that manufacture or market products discussed in this activity. Faculty disclosures will be announced at the beginning of the CE activity.

Please note: The information and views presented in this activity are those of the faculty through clinical practice and knowledge of the professional literature. Portions of this activity may include the use of drugs and/or devices for unlabeled indications, which should be considered experimental. Participants are advised to consult manufacturer product information and the professional literature, and use professional judgment in applying the presented information in patient-care activities.

Funding

This activity is supported by an educational grant from ICU Medical.

 

Equipment Requirements
-Computer with broadband Internet access
-Soundcard and speakers or headphones for your computer (or dial-in via telephone for audio)
Click here for detailed software requirements.

After registering you will receive a confirmation email containing information about joining the Webinar.

The material presented in this CE activity does not reflect the views of ProCE, Inc. or the commercial sponsor. These materials may discuss uses and dosages for therapeutic products, processes, procedures and inferred diagnoses that have not been approved by the United States Food and Drug Administration. A qualified health care professional should be consulted before using any therapeutic product discussed. All readers and continuing education participants should verify all information and data before treating patients or employing any therapies described in this continuing education activity.