Clinical Research Monitoring Visits and Common Issues Explained

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Dan Sfera

Dan Sfera

5 жыл бұрын

Clinical Research Monitoring Visits and Common Issues Explained
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Пікірлер: 14
@maryamzarei8274
@maryamzarei8274 6 ай бұрын
Thank you Dan🎉
@aprilchen8042
@aprilchen8042 5 жыл бұрын
very useful, Thanks Dan
@dansfera
@dansfera 5 жыл бұрын
thanks!
@BucurEST1989
@BucurEST1989 11 ай бұрын
Thank you
@Christyle09
@Christyle09 5 жыл бұрын
Very helpful, Dan! Thank you. I’m taking notes.
@dansfera
@dansfera 5 жыл бұрын
thanks, good luck at your new job!
@gadeboye2001
@gadeboye2001 5 жыл бұрын
How do you conduct a typical " Protocol Training" is there a format given by the Sponsor
@dansfera
@dansfera 5 жыл бұрын
Sometimes but usually is just a training however the cra sees fit and documented as per sponsor or cro sop
@umairamin1229
@umairamin1229 3 жыл бұрын
@@dansfera Can you elaborate on this, please? I'm thinking, "how do you conduct protocl training in 30 minutes?" Thanks.
@reyyajacob1049
@reyyajacob1049 4 жыл бұрын
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 4 жыл бұрын
Usually yes
@zouhairallali6414
@zouhairallali6414 3 жыл бұрын
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
@odwarotobias706
@odwarotobias706 8 ай бұрын
What is the minimum for a site to be activated?
@dansfera
@dansfera 8 ай бұрын
Irb approval and all docs. One week.
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