For companies who export food or drug related products to the USA, CSE are able to offer US Food and Drug Administration (FDA) Code of Federal Regulations Title 21 CFR Part 11 (21 CFR Part 11) compliant IT based solutions.

Firstly published in 1977, the regulations state that the Food and Drug Administration (FDA) accepts electronic signatures and records provided they comply with 21 CFR Part 11 compliant.

Combining CSE's expertise in providing turnkey solutions for the process industry, with our knowledge and experience in implementing applications required to be 21 CFR Part 11 compliant, our customers can feel safe in the knowledge that their project is being coordinated from one professional customer focused engineering team.

Our Project Engineers will work closely with you to understand the issues that affect your day-to-day business with the objective of providing a solution that is tailored to your specific requirements. CSE believe that the best way to understand is to listen. We listen to our customers, understand their particular concerns, anticipate their needs and design the most cost effective business solution for them, using the most up to date technology.

For further information, please contact sales@cse-globaluk.com.