(*good laboratory practice)
In many laboratories, the need for stringent documentation of quality control and assurance becomes more and more relevant. We estimate that at least 10% of all samples tested in the pharmaceutical industry must be run according to GLP. Furthermore, GLP compliance is a prerequisite for many accreditation efforts.
TSE Systems can assist your GLP compliance by providing the following:
Speak to your local representative for further details or use the contact form.