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Validation method
references for Alconox detergents
A cleaning validation involves testing for acceptable residues on pharmaceutical manufacturing or medical device surfaces. The validation involves residue identification, residue detection method selection, sampling method selection, setting residue acceptance criteria, methods validation and recovery studies, and finally writing a procedure and training operators. This procedure is used to document acceptable residues 3 or more times and then a rational monitoring program to maintain a validated state is put in place. If you are changing any part of your procedure or cleaner, first clean the new way, collect data and then clean the old way before using any equipment while you are in the process of validating the new procedure.
Click
here to read detailed descriptions of each step!
Optimizing
critical cleaning products for quality assurance, safety, and
reproducibility of results starts with good science. With over
50 years of experience in the critical cleaning field, Alconox
can help you meet validation guidelines. We will help
you find the best cleaners and procedures for your applications.
This
information is presented to help communicate our understanding
of how validation has been carried out in
pharmaceutical and medical device processing. The information
given here is made without any representation or warrantee, as
it is presented for your own investigation and verification.
Request a technical bulletin for a chemical description of the
ingredients in each Alconox, Inc. detergent.
To
speak to a technical representative about validation,
call 914-948-4040 for Malcolm McLaughlin (x160) mmclaughlin@alconox.com
or Phyllis Horata (x151) phorata@alconox.com.
To request a free sample
pack of Alconox detergents you can call (914) 948-4040 or
use the detergent
selection system and sample request form on our site.
To place an order for our
cleaning products follow this link:
Buy
Alconox Products
or call your laboratory,
healthcare, or industrial supply company.
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