ISO 14155 training for CRAs
European Centre for Clinical Research Training (ECCRT)
Archive
22.05.2014 Brussels, Belgium
Course Content
You are a monitor who needs to understand the counterpart of ICH-GCP for medical device trials. You want to know the rules and responsibilities outlined in ISO14155 and get some practical advice and hints and tips on improving your monitoring skills? This course is made for you and your colleagues!
You are a monitor who needs to understand the counterpart of ICH-GCP for medical device trials. You want to know the rules and responsibilities outlined in ISO14155 and get some practical advice and hints and tips on improving your monitoring skills? This course is made for you and your colleagues!
Learning objectives, training objectives
To understand the role of clinical studies in the development of devices
To be familiar with the basic requirements on how clinical trials are carried out
To appreciate the device-specific study elements as compared to drugs studies
To understand the role of clinical studies in the development of devices
To be familiar with the basic requirements on how clinical trials are carried out
To appreciate the device-specific study elements as compared to drugs studies
Target Audience
Recently started CRAs or Investigators and study co-ordinators.
Recently started CRAs or Investigators and study co-ordinators.
Certifications
ISO 9001:2008 / Q-for
ISO 9001:2008 / Q-for
Local Organizer
European Centre for Clinical Research Training
European Centre for Clinical Research Training
Enquiries and Registration:
Ms. Sunita Kelecom
Clinical Research
Organizer contact info
Marcel Broodthaers plein 8b5
1060 Brussels
Belgium
Marcel Broodthaers plein 8b5
1060 Brussels
Belgium
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