Feb 16, 2024

Saving Energy in a Pharmaceutical Cleanroom

Jan 31, 2024

Continuous Microbial Monitoring

Jan 18, 2024

21 CFR Part 11 – Electronic Records Signature

Dec 19, 2023

Cleanroom Design Considerations from a NASA Engineer

Dec 19, 2023

EU GMP Annex 1 Continuous Viable Monitoring

Dec 19, 2023

Pharma 4.0: Revolutionizing the Aseptic Manufacturing Process

Oct 25, 2023

Understanding ISO TR 14644-21

Jul 26, 2023

Cleanroom Behavior According to ISO 14644

Jun 15, 2023

Fill in the GAP Good Application Practices – How to classify cleanrooms?

May 11, 2023

USP Overview with guest USP speakers: Rebecca Cambronero and Desmond Hunt Part 2

Apr 26, 2023

USP Overview with guest USP speakers: Rebecca Cambronero and Desmond Hunt – Part 1

Mar 30, 2023

How To Prepare A Contamination Control Strategy Document as Per New GMP Annex 1

Jan 26, 2023

How Do Compounding Pharmacies Utilize Environmental Monitoring.

Nov 23, 2022

Microbiology & Bio contamination Control in Cleanrooms From EN ISO 14698 to a new EN 17141

Nov 7, 2022

Overview of GMP Annex 1 and its impact on Environmental Monitoring

Sep 22, 2022

Cleanroom Validation from URS to PQ; ISPE GAMP5 2022 Edition & V Scheme Application for Cleanroom Monitoring Systems

Aug 26, 2022

Using Real Time Monitoring Systems in the Semiconductor Industry to Increase Product Yield

Jul 27, 2022

Cleanroom Monitoring Explained ; How, when, and why do we do the monitoring in cleanrooms?

Jun 30, 2022

What is 21CFR11 and why is it so important in maintaining Data Integrity?

May 18, 2022

Fill the “GAP” Good Application Practice “How to Test HEPA Filters ”

Apr 28, 2022

What is GAMP and why is it so important in Cleanroom Manufacturing?

Mar 23, 2022

Good Application Practice: How to Perform Proper Cleanroom Classification

Feb 23, 2022

Understanding and Applying USP 788 Best Practices

Dec 21, 2021

Digitalize Your Environmental Monitoring Contamination Control Strategy

Dec 15, 2021

How to Effectively Implement an Environmental Monitoring System Part 2: The Validation and Handover Process

Nov 24, 2021

How to Effectively Implement an Environmental Monitoring System Part 1: The Installation Process

Nov 3, 2021

Particle Counting Fundamentals

Oct 27, 2021

Microbiology & Bio contamination Control in Cleanrooms

Sep 27, 2021

Active Air Sampling Technology & ISO 14698

Sep 22, 2021

How to validate your Cleanroom. HVAC Performance Qualification Basics.

Sep 8, 2021

ISO 14644-1:2015 and ISO 14644:2-2015 Review

Jun 29, 2021

Using a Risk Assessment to Build a Monitoring System Focusing on Data Integrity

Jun 23, 2021

EN17141 “Bio contamination Control” and Microbiology in Cleanrooms & Controlled Environments

Jun 16, 2021

Let’s Prepare an ISO 14644-1 and GMP Annex 1 Cleanroom Classification Report Together

Jun 16, 2021

Fill in the “GAP”; Good Application Practices – “How to Test HEPA Filters?”

May 26, 2021

Preventing Downtime With Liquid Particle Counting Technology

May 13, 2021

GMP Annex 1 2020 Draft: Effects on cleanroom classification and monitoring

Apr 22, 2021

Your Key to Success: Building a Contamination Control Strategy

Apr 15, 2021

Particle Monitoring- How To Go Paperless in The Cleanroom

Mar 17, 2021

How to Prepare a Risk Based Cleanroom Monitoring Plan as per ISO 14644-2:2015

Feb 17, 2021

Understanding Particle Counter Calibration in Less Than 45 Minutes

Feb 5, 2021

ISO 14644-3:2019 Cleanrooms and Associated Controlled Environments-Test Methods

Jan 22, 2021

GMP Annex1 2020 Draft and its Effect on Cleanroom Classification and Monitoring

Aug 26, 2020

Prevent Failure by Designing Your Cleanroom Monitoring System to Meet cGMP

Jul 22, 2020

Performance Qualification of Environmental Monitoring Systems

Apr 15, 2020

Particle Monitoring – Going Paperless in the Cleanroom

Jul 17, 2019

ISO 14644:2-2015 Creating, Implementing, and Maintaining a Monitoring Plan