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Analysis of contamination in pharmaceutical products

The need to understand contamination of pharmaceutical materials is extremely important. At best, the contamination may only be cosmetic, perhaps leading to returned product. At worst, the consequences of contamination can be fatal.

Contamination can occur at any stage of product manufacture and can arise from the raw materials, cleaning materials, chemicals or equipment used in production and packaging or from degradation during storage. It can be inorganic or organic in nature and in solid or liquid form.

In many cases, the contamination is due to visible or sub-visible particulate matter, and we are able to identify and count such particles.

There are many other forms of contamination however. Other examples include:

  • Degradation of API or excipients
  • Matter coming out of solution
  • Change of polymorphic form or presence of other polymorphic forms
  • Residual solvents
  • Discoloration of tablets
  • Discoloration or films on production equipment.

 

 

We have many years experience in solving contamination problems for the pharmaceutical industry, and have a wide range of analytical techniques at our disposal to help in the identification of contaminants.

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For further information, contact us:

Email: pharmaInfo@lgc.co.uk 

LGC, The Heath Business Park, Runcorn, Cheshire WA7 4QX, UK

Tel: +44 (0)1928 515163

Fax: +44 (0)1928 500125

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