Validation – SiQuest – Contamination Control Specialist

Articles & News

Understanding Biofilm Lifecycle and Remediation Procedures

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

09
Nov

Articles & News

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

Webinar

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

Webinar

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

Webinar

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

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

Understanding Biofilm Lifecycle and Remediation Procedures

Factors to Consider for a Cleaning and Disinfection Program

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

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

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

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

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