ISO14155 E-learning training
if you would like to be MDR compliant!
This training is especially important for any party involved in clinical investigations with medical devices, who are looking for answers on how to practically implement the Good Clinical Practice into their daily practice.395 - 695
4 Punten
E-learning
Prijzen
Variabel € 395 - 695
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Doelen
Upon completion of this training, you will be able to correctly and successfully:
Comprehend and apply the requirements of the ISO 14155 as a GCP guidance specifically for medical device clinical investigations from start to finish
Understand how risk management is applied to all aspects of medical device clinical investigations
Comprehend the different types of clinical investigation study designs and how ISO 14155’s requirements apply
Adapt your procedures to the new requirements compared to the ISO14155:2011 version
Omschrijving
In this e-learning you will get valuable, state-of-the-art information on the interpretation and implementation of the Good Clinical Practice in your clinical investigations with medical devices.
You learn how to:
• add credibility to your clinical data
• protect your subject’s rights & safety
• worldwide acceptance of your data
• no more findings during inspections
• avoid unnecessary risk for patients
• avoid unnecessary regulatory delay
• implement the regulation
• including practical solutions
Rianne Tooten
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