Cleaning Validation for Pharmaceutical Manufacturing

Cleaning Validation for Pharmaceutical Manufacturing

Image Credit: Jordi Labs

In pharmaceutical manufacturing, cleaning validation is an essential stage of verifying that the manufacturing process is suitable.

As an integral stage of the cleaning validation program, analytical testing of residue after the cleaning procedure offers scientific evidence to prove that the residue has been decreased to an acceptable level.

This whitepaper outlines the main aspects and overall steps for a chemical cleaning validation.

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About Jordi Labs

Jordi Labs provides the highest quality contract analytical services and polymer HPLC columns to some of the world’s leading consumer products, polymers, pharmaceutical and medical device manufacturers. Our team of PhD analytical chemists specialize in chemical identification. One of core competencies is Extractables & Leachables testing.

We are also worldwide leaders in;

  • Particulates & residue analysis
  • Good-bad comparisons
  • Method development/validation
  • Polymer analysis
  • Polymer failure

We also help companies from Fortune 500s to innovative startups with method development, preparative HPLC, training seminars, depositions and consulting. As a family company, we take pride in the production of all of our products and analytical service offerings. It is our goal to help our customers overcome their analytical challenges by providing excellent products and personal assistance from our highly-trained staff of PhD chemists.


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Last updated: Oct 1, 2020 at 5:09 AM

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