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Will begin shipping
on March 31, 2009.

The update includes
sections on the new
provisions of the 2008
Standard update and
continues to remain the
audio-visual component
of the ACPE-accredited,
VALITEQ Aseptic
Technique Verification
Program.

 

Your complete, closed-loop,
Quality Management System for
Compounded Sterile Products

Proper use of the VALITEQ®, ChemoTEQ™, and
SteriTEQ™ compounding validation systems assures
quality management of your CSP programs in
accordance with the USP Standard <797>. Our
pharmacy-friendly systems will produce outcomes
which are necessary to demonstrate Continuous
Quality Improvement (CQI) and quality assurance
of your pharmacy and non-pharmacy CSP programs
and activities. In addition, this standardization of
your CSP activities will improve the morale of CSP
operatives and simplify your routine quality data
acquisition tasks.

Learn about the verification procedure.
Get the straight talk about pharmacy validations.

Step 1

 

Where Do
I Begin?

Learn how to:
Design a Verification Program
Design a CSP Facility
Implement USP <797>
and much more.

Get Started

NIOSH Compliance

 

How Can I
Achieve NIOSH Compliance?

Help is available:

Safe Compounding of
Hazardous Drugs Manual

ChemoTEQ™ Hazardous Compounding Verification Kit

Design Consultation
for a Three-Cell Clean
Compounding Space

ChemoVallet

ChemoValet Ventilated Storage with Refrigeration