Changes to the USP: Are you Ready?

Use the contract laboratory prepared for USP changes. Celsis.

The harmonization of USP chapters has resulted in many changes affecting manufacturers of pharmaceutical products and ingredients. The complexity involved in meeting each new procedure costs your company time and money. At Celsis, we're prepared, so you can rest assured.

USP <61> Microbial Enumeration - Revisions effective 1 May 2009 and
USP <62> Absence of Specified Organisms - New chapter effective 1 May 2009

We are already helping customers validate and qualify their materials for these requirements. How can we help you prepare?

Educational resources:

• Media Alert: Celsis Outlines 12 Key Steps to address USP Chapters <61> and <62> Changes (PDF 53.5KB)
• FAQs for submitting suitability samples
• White Paper Concerning Changes to USP <61> and
  USP <62> (PDF 27.5K)
• View our Dec 10th, 2008 webcast on demand
• View slides from our Dec 10th, 2008 webcast (PDF 6.6MB)
• View Q&A from our Dec 10th, 2008 webcast (PDF 72KB)

USP <467> Residual Solvents - Revisions effective 1 July 2008

We have implemented compliant testing procedures and meet all system suitability requirements.

Educational resources:

•  White Paper Concerning Changes to USP <467>  (PDF 22.7KB)
• PowerPoint slides from the 22 April 2008 webcast <467>  (PDF 1.76MB)
• Celsis USP <467> Media Alert (PDF 39.1KB) 

Are your products meeting the new USP requirements? We're prepared to help. Contact Celsis Analytical Services today.