Life Sciences and Healthcare
Fulfil certification regulations
Both Pharmaceutical and Biotech industries are tightly regulated industries and as with all aspects of drug manufacturing,
all actions preformed within software testing and QA must conform to current Good Manufacturing Practices.
This is enforced by pharmaceutical regulators within particular countries, for example the US Food and Drug Administration
(FDA) and the UK's Medicines and Healthcare products Regulatory Agency (MHRA).
Software is a central element in
almost all technical production processes. When developing software for use in the manufacture of pharmaceuticals, medical
technology and diagnostics, these particularly strict safety requirements apply.
SQS has specialist knowledge of these
requirements and regulation and can therefore help in authenticating and validating all software for pharma-engineering
processes or for medical technology products in accordance with the relevant standards. Through systematic and automated
test procedures, SQS can guarantee that your software fulfils all tasks reliably and to the required quality standard.
