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Education Track Sessions

  • Sterile Compounding
  • Wednesday  |  
  • 3/27/2024  |  
  • 10:15 AM – 
  • 11:15 AM
  •   |  Room: Austin Conv Ctr 18 CD

Cleanroom Design: Where to Start

This presentation will cover the basis for where to begin planning when deciding to create a new cleanroom or redesign an existing cleanroom location to better meet the USP and cGMP requirements. Listeners will leave the presentation with an understanding of a stick model of what to consider in order to ensure compliance with all standards.
This presentation will cover the basis for where to begin planning when deciding to create a new cleanroom or redesign an existing cleanroom location to better meet the USP and cGMP requirements. Listeners will leave the presentation with an understanding of a stick model of what to consider in order to ensure compliance with all standards.

Learning Objectives

  • Conduct gap analysis focusing on new construction and existing construction.
  • List the basic requirements for designing a cleanroom space and which list sources to use to assist with understanding the requirements.
  • Describe the thought process for design decisions using a stick diagram.

    • Speaker(s)

    Kathleen Kane PharmD; BCSCP
    Assistant Director of Pharmacy; Compounding Integrity and Compounding Regulatory Compliance
    University of Chicago Medical Center

    Jessica Hawkins PharmD, BCPS, BCSCP
    Pharmacy program manager- sterile compounding
    Lexington VA Health Care System

    Speaker
    Kathleen Kane PharmD; BCSCP
    Assistant Director of Pharmacy; Compounding Integrity and Compounding Regulatory Compliance
    University of Chicago Medical Center
    Speaker
    Jessica Hawkins PharmD, BCPS, BCSCP
    Pharmacy program manager- sterile compounding
    Lexington VA Health Care System

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    Registration for the Sterile Compounding Clinic Required