Increasing Safety and Minimising Risk
Medical devices and IVD’s success in the market are reliant on the function and safety of the product. Detailing each process, creating traceability, solving problems and building a robust QMS in ISO:13485 is integral to the ongoing success of any company. Quality Assurance teams have evolved over the last 10-15 years as standards have evolved and notified bodies are now able to conduct unannounced audits.
Vado Med Tech have exceptional knowledge of this key function and typically have opportunities in the following areas: