Clean Room 10 Offer

10% Offer

Thank you for your interest in environmental monitoring for your Clean Room, Compounding Pharmacy, or Clean Manufacturing application. From now until the end of the year request a quote for your monitoring needs and receive that offer with 10% off Hardware and Services list price. The offer is exclusive of hosting, support, software, and/or travel expenses. This offer is in effect until December 31st, 2019 and quotes are valid for 30 days.

Contact us now by clicking here and requesting a quote.  Be sure to include “Clean Offer 10” in the comments.

Clean Rooms & Regulated Manufacturing

Pharmaceutical Manufacture & Storage • Medical Devices • Semiconductor & Delicate Instruments

One system continuously monitors the environment in cleanrooms as well as the condition of the supporting infrastructure. SmartScan can be used to implement a Clean Room Monitoring System that is fully cGMP-Compliant including Temperature and Humidity Monitoring, Differential Pressure Monitoring, and Airborne Particle Monitoring. The system meets ISO 14644 requirements and conforms to the data integrity stipulations specified in FDA 21 CFR Part 11.

ISO 9001/2015 Certificate                  ISO 17025/2017 Certificate

Perry Johnson Laboratory Accreditation, Inc. Logo

• Mobile & Web-Based User Interface:
A simple web browser is all that you need to interface with SmartScan.
• Use Existing Network Infrastructure
Significantly reduce the installation cost and minimizes the disruption to current operations.
• Requires Minimum IT Involvement
Your company already supports the IT infrastructure and we’ll support the SmartScan application. You can host the system or we also offer a Cloud hosted option.
• Data Loss Prevention
No measurement data is ever lost due to network interruptions because of the SmartScan system’s fault tolerant design.
• Meets Regulatory Requirements
Meet all the requirements contained in FDA 21 CFR Part 11, EU Annex 11, and ISO 14644. In addition, a variety of standard reports quickly give auditors what they need.
• Easily Validated
Our inexpensive but solid validation methodology can be easily and completely validated in days, not weeks.
• Enterprise-Wide
Monitor a cleanroom in New Jersey, a laboratory in the UK, and an organization doing clinical trials in South Carolina, all with the same system. Access is easily restricted to individuals on a “need to know” basis.

Suggested Monitoring Points

Looking for guidance? Let us help you get started.

System Features

Downloads

Cleanroom Monitoring Brochure

Cleanroom Components Selection Guide

or to download

Learn More about Applications for Cleanrooms and Regulated Manufacturing

How to Obtain Particles per Cubic Meter Measurements in a Timely Manner

Cleanrooms for R&D and Manufacturing

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