Rob Cheesman featured in The CEO Magazine
Read below in The CEO Magazine about how Rob Cheesman our General Manager discovered an invaluable community of...
There are thousands of medical devices and pharmaceutical companies in the region. With a significant focus on improving health and an ageing population, the industry has never looked stronger.
With challenges ranging from innovation, product quality and patient safety, a tightening regulatory environment, increasing cost pressures and supply chain complexities, having partners who can guide you is critical.
QAD provides a comprehensive yet flexible solution. Cloud based, FDA-qualified environments reduce the effort required for software validation and 21 CFR Part 11 and Annex 11 compliance. They also support traceability, ISO 13485, FDA QSR and EU MDR requirements.
Kettering’s industry experience, especially our knowledge of the process to validate your software to satisfy FDA and TGA helps you remain relevant in this ever-changing world.
Read below in The CEO Magazine about how Rob Cheesman our General Manager discovered an invaluable community of...
Key highlights: Atturra expands QAD sales and service operations in Australia More than 20 additional QAD...
Kettering Professional Services has joined ASX-listed, leading advisory and technology solutions provider Atturra...