Client Interview – Shaundra Biggs – Aroa Biosurgery
Last month we had the pleasure of sitting down with Shaundra Biggs, Director of Enterprise Business Systems at Aroa...
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.
Last month we had the pleasure of sitting down with Shaundra Biggs, Director of Enterprise Business Systems at Aroa...
Key highlights: Kettering Professional Services will be acquired by Atturra a leading Australian owned,...
The very lucky staff who worked for Kettering in 2008 had this phone as our standard issue. It was pretty amazing...