received product quality complaints, adverse events and medical enquiries to the relevant person in quality
received product quality complaints, adverse events and medical enquiries to the relevant person in quality
relevant parties of Serious Adverse Events or Events of Medical Importance as per protocol requirements.
relevant parties of Serious Adverse Events or Events of Medical Importance as per protocol requirements. Quality
relevant parties of Serious Adverse Events or Events of Medical Importance as per protocol requirements. Quality
going to work events, no PrDP required) Previous work experience within an Emergency Medical Services environment
workshops, partnering with the Event Specialist of the Region, Medical Affairs and local sales teams to
workshops, partnering with the Event Specialist of the Region, Medical Affairs and local sales teams to