Webinar

Disinfectant Validation and Efficacy Testing

  • Date: Wednesday November 25, 2026
  • Time: 12:00 pm – 1:30 pm (NY Time)
  • Instructor(s): Jim Polarine
  • Webinar ID#: ECC-751
Webinar Details:

This presentation covers current debates and challenges in the industry regarding disinfectant coupon testing and disinfectant field trials. Annex I (2022), PDA Technical Report No. 70, IEST RP 018.6, and current USP <1072> will be covered in relation to current industry disinfectant efficacy testing and disinfectant field trials. Recent FDA Warning Letters and 483s will be covered that highlight regulator expectations in disinfectant efficacy testing. Data will be presented covering the importance of disinfectant efficacy testing with specific bacterial spores which can be more difficult to kill than ATCC strains. Both sides of the debate on disinfectant validation will be covered in detail with an emphasis on current FDA, MHRA, ANVISA, ANSM, CFDA, and HPRA regulatory expectations and reducing the costs for testing. The recent USP current <1072>, PDA Technical Report No. 70 recommendations on DET (Disinfectant Efficacy Testing) will be discussed.

Who Should Attend the Webinar:

  • Validation Managers
  • Quality Control Managers
  • Quality Assurance Managers
  • Lean Managers
  • Operations Managers
  • Cleanroom Managers
  • Regulatory Affairs Managers
  • Production Managers
  • Quality Systems Managers
  • Sustainability Managers
  • Continuous Improvement Managers

Fee:
$385 for one person
$700 2-5 people
$999 6-10 people

Register for ECC-751