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PDA Missouri Valley Chapter Webinar: A Risk Based Cleaning and Disinfection Program

May 26, 2020
Online,

  • Virtual
  • Chapter
  • Online

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Overview

You are invited to join the PDA Missouri Valley Chapter for it's inaugural free morning webinar talk on leading design techniques for a Risk Based Cleaning and Disinfection Program. Attendees will learn the latest advances in cleaning application tools and disinfectants and sporicides in the industry.

This webinar will cover designing a risk-based cleaning and disinfection program during the COVID-19 pandemic. The presentation will bring clarity to the cleaning and disinfection process by covering current industry trends, global regulatory expectations, and essential elements needed to keep the cleanroom in a state of control. There will be an in-depth discussion on current regulations, disinfectant and sterilant technologies, operator safety, and applications of these products. Videos will be shown to cover the usage and application techniques with these products. Current industry trends in disinfectant rotation, sterility, application techniques, and rinsing will be discussed. Regulatory expectations of FDA, MHRA, ANVISA, ANMAT, HPRA, EMA, and ANSM inspectors will be addressed. The current draft Annex I, USP 43 <1072>, PDA Technical Report #70, and other industry guidance documents will be covered. The attendees will gain a more robust understanding of current industry trends regarding cleaning and disinfection best practices and how to design an effective risk-based program. Current industry FDA Warning Letters and FDA 483s will be covered as teaching tools.

Agenda

    • Current Regulations, Guidance Documents (Annex I) related to cleaning and disinfection
    • Latest technologies, application frequencies and methods for disinfectants
    • Best practices in writing effective SOP’s
    • Disinfectant rotation and rinsing strategies.

Highlighted Speakers

Jim N. Polarine
Jim N. Polarine
STERIS Corporation

Additional Information

  • Learning Objectives

    Learning Objectives

    More information coming soon.

  • Who Should Attend

    Who Should Attend

    This webinar is intended for professionals who are involved in the development and assessment of sterilization processes used in sterile drug manufacturing.

    Departments
    • Quality Systems
    • Engineering
    • Manufacturing
    • Quality Assurance Operations
    • Technical Operations
    • Validation

    Roles
    • Cleanroom Managers
    • Lean Managers
    • Operations Managers
    • Production Managers
    • Quality Assurance Managers
    • Quality Control Managers
    • Quality Systems Managers
    • Regulatory Affairs Managers
    • Validation Managers

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Travel

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Virtual Meeting


Online,

How to Get Here

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By Car

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Other Options

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Directions

Registration Fees

Regular Price
Registration Type Price
Member FREE
Non-Member FREE

* For this member type or discounted rate, online registration is not available and must be faxed in.

† You must be a member to receive this rate.

All rates in US dollars. To receive the prevailing rate, PDA must receive your registration(s) by 5:00 p.m. ET on or before the date noted.

Group Registration Discount

Register 3 people from the same organization as a group (at the same time) for the Conference or Workshop and receive the 4th registration free. Other discounts cannot be applied.

Special Dietary Requirements

If you require special accommodations and/or have special dietary requirements, please state them in the appropriate field when you register for the event(s).

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REFUND: If a refund request is sent 30 days before the event, a full refund will be given minus a $200 fee. After this period, no refunds will be given. Refund requests must either be faxed to + (301) 986-1093 or emailed to [email protected]. Phone messages are not accepted.

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