Industry

We help drug manufacturers bring the best possible product to market, in full and demonstrable compliance with the latest GxP standards.
We tailor our offerings to meet the distinct requirements of each client, by offering a comprehensive suite of consulting and advisory services, including quality management systems, mock inspections, equipment qualification and computerized system validation.

We provide integral support for all stages of product and software lifecycle, including in-vitro diagnostic products and medical device software (MDSW) in Europe and USA. With us, you can rest assured that your medical device (MD) regulatory compliance needs are taken care of, allowing you to focus on your core business objectives.