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Clinical Research Monitoring Visits and Common Issues Explained 

Dan Sfera
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Clinical Research Monitoring Visits and Common Issues Explained
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2 окт 2024

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Комментарии : 15   
@aprilchen8042
@aprilchen8042 6 лет назад
very useful, Thanks Dan
@dansfera
@dansfera 6 лет назад
thanks!
@Christyle09
@Christyle09 6 лет назад
Very helpful, Dan! Thank you. I’m taking notes.
@dansfera
@dansfera 6 лет назад
thanks, good luck at your new job!
@odwarotobias706
@odwarotobias706 10 месяцев назад
What is the minimum for a site to be activated?
@dansfera
@dansfera 10 месяцев назад
Irb approval and all docs. One week.
@maryamzarei8274
@maryamzarei8274 9 месяцев назад
Thank you Dan🎉
@BucurEST1989
@BucurEST1989 Год назад
Thank you
@reyyajacob1049
@reyyajacob1049 5 лет назад
Hi, I am a pharmacy graduate from India and have more than a year's experience as a CRC. Do I need to study an international course to work abroad in the field of clinical research?
@dansfera
@dansfera 5 лет назад
Usually yes
@zouhairallali6414
@zouhairallali6414 3 года назад
there is no such international course for CR because each country has its own laws and regulations so you have to decide which country you want to work for and then take a CR course in that particular country
@gadeboye2001
@gadeboye2001 5 лет назад
How do you conduct a typical " Protocol Training" is there a format given by the Sponsor
@dansfera
@dansfera 5 лет назад
Sometimes but usually is just a training however the cra sees fit and documented as per sponsor or cro sop
@umairamin1229
@umairamin1229 3 года назад
@@dansfera Can you elaborate on this, please? I'm thinking, "how do you conduct protocl training in 30 minutes?" Thanks.
@HeyyyItsEdgar
@HeyyyItsEdgar 23 дня назад
@@umairamin1229protocol overview, primary endpoints, safety training, device management and set up, documentation could be covered in that time
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