Cleaning Validation Virtual Summit | Feb 10 & Feb 11 2021| ONLINE

Join our experts at the upcoming virtual Cleaning Validation Summit hosted by PharmaEd Resources Inc.

03
Feb
Solutions for Protecting Gloves in Cleanrooms and Critical Environments

Personnel are typically the primary source of contamination in cleanrooms. This is true at pharmaceutical,

03
Feb
PDA Australia Chapter: Validation and Cycle Requirements for GMP Autoclaves | 09 Feb 2021, 8.00 AM – 9.30 AM (GMT +08) | Online

The PDA Australia Chapter are delighted to invite you to join our first event for

02
Feb
Understanding Biofilm Lifecycle and Remediation Procedures

Biofilm formation in process equipment presents challenges and may lead to serious consequences in GMP

09
Nov
Factors to Consider for a Cleaning and Disinfection Program

An effective cleaning and disinfection program is critical to controlling the bioburden in a cleanroom.

02
Nov
Cleaning Validation – Sterile Environments Regulatory Trends | 10 Nov 2020, 8 – 9.30PM | Online Session

The FDA conducted approximately 17,671 inspections in Fiscal Year 2018, amounting to roughly 1400 inspections/month

01
Nov
Steam Sterilization & Autoclave Performance Qualification 20 Oct 2020, 8-9.30pm | Online Session

This workshop will provide an overview of microbiology principles in steam sterilization and application, as well as autoclave Performance Qualification, regulatory

10
Oct
Points to Consider for Disinfectant Efficacy Studies 8 Sep 2020, 5 – 6.30pm | Online Session

This presentation will focus on the current regulations, guidelines, method and standards available for disinfectant

30
Aug