PaperControlling Quality in Advanced Optics Manufacturing

Controlling Quality in Advanced Optics Manufacturing

This FAQ paper is a follow up to the webinar Controlling Quality in Advanced Optics Manufacturing. During this webinar there were many good questions about monitoring contamination in clean optics manufacturing environments. Many of these questions were answered during the webinar and a few were submitted later. Please read below to see all the webinar questions, or submit your additional questions directly to us.

PaperCleanroom Validation and Qualification

Data Management Series 3 – FMS PC-based Logic Versus Industrial Automation Design

The scope of this document is to describe the difference between PC-based logic and industrial automation design.

PaperParticle Monitoring Frequency: Frequent or Continuous (Series Part 2 of 4)

How to Test Particle Transportation in Tubing for Particle Counters

Papercleanroom sample locations

Are Your Particle Monitoring Sample Points Optimized?

The Particle Measuring Systems (PMS) environmental system designers are often asked how to choose clean room sampling points, whether it be performed in a pharmaceutical cleanroom or clean device (RABS, isolator, etc.).

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