Are you a disruptive medical device technology innovator searching for reliable quality or regulatory support?
I break down the complexity of the applicable medical device regulations and standards and deliver tailor-made solutions that work for you (considering your timescale, resources and available budget). In a nutshell, I do the work, so you don’t have to. My aim is to reduce your workload, remove stress, and to provide clarity and confidence concerning your organisation’s quality and regulatory obligations. My services ensure that your organisation is consistently audit-ready and that the safety and performance of your medical device is assured.
What I Do
Quality Management Systems
Supplier and Internal Auditing
Strategy development and execution
How Can I Help Your Project?
If you are a medical device innovator who demands excellence, then contact Neasa Greene Consulting today for an initial consultation.