IV Sterile Compounding Risks and Safety

Speaker

Instructor: Scarlett Eckert
Product ID: 706464

Location
  • Duration: 90 Min
This webinar will discuss the risks in IV sterile compounding and how to mitigate those risks. We will review the safety requirements in USP <797> and USP <800>, to ensure the safe compounding of CSPs and protection of the patient and compounding staff.
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Why Should You Attend:

  • Do you know the key risk factors when compounding sterile CSPs?
  • Do you know the main source of contaminates entering the cleanroom?
  • Do you understand regulatory requirements for safe compounding of sterile CSPs?
  • Do you know how to protect yourself and your staff from hazardous drug exposure?
  • Do you know how to protect the general public from hazardous drug exposure?

This webinar will explain the proper handling of NIOSH listed drugs from receiving to disposal and all handling processes in between: storage, dispensing, compounding.

Learning Objectives:

  • Review the severity of IV compounding errors.
  • Review the New ‘proposed’ USP <797> requirements addressing IV compounding safety.
  • Review the USP <800> personnel, environment and patient safety requirements.
  • Describe the components of IV compounding errors.
  • Identify which risk factors and safety issues can be mitigated.
  • Discuss how to mitigate risk factors and improve safety of your cleanroom practices and compounded sterile products.

Who Will Benefit:

  • Pharmacist, Pharmacy Technician, Physician, Nurse, Health Clinic Staff, Retail Pharmacy Staff, Physician Office Staff

Free Materials:

  • Copy of Power Point Slides
Instructor Profile:
Scarlett Eckert

Scarlett Eckert
Independent Consultant, Eckert Healthcare Consulting

Dr. Eckert received her Doctor of Pharmacy degree from the University of the Pacific, in Stockton, California. Scarlett is currently working as an independent consultant pharmacist.

She is an expert on pharmacy regulatory requirements including USP Chapter <797> Pharmaceutical Compounding – Sterile Preparations, current and proposed revision and USP <800> Hazardous Drugs – Handling In Healthcare Settings. She has completed certification in Aseptic Process and Compliance Tools for USP <797> and USP <800> Safe Handling and Preparation of Cytotoxic and Other Hazardous Drugs from the Baxa Star Center, Parker, Colorado, and Best Practices for Handling Hazardous Drugs (USP 800) from the Clinical Point Training Center, Totowa, NJ. She participated on the ISMP IV Safety Summit in 2011.

Dr. Eckert specializes in working with individual hospitals, large health systems, specialty compounding centers in understanding and how to implement USP Chapters regulations and develop safe sterile compounding practices in the Unites States and Canada.

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