Elemental Impurity Analysis in Pharmaceuticals.free download from Butterworth labs

Posted on

New Drug Approvals

Contract Analytical Chemistry Services and Quality Control Testing logo

Elemental Impurity Analysis in Pharmaceuticals

A method to identify the presence of heavy metals in pharmaceuticals was introduced in the United States Pharmacopeia more than 100 years ago.

Pharmaceutical companies are still using essentially the same method, known as the USP Heavy Metals Limit Test.

This paper will provide an overview of current method limitations, considerations for the new methodology and risk-based assessments being carried out by manufacturers.

Available Downloads

  • Elemental Impurity Analysis in Pharmaceuticals 
    Download

View original post

Advertisements

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s