Clinical Research Monitoring Visits and Common Issues Explained

[@maryamzarei8274]

Thank you Dan🎉

[@aprilchen8042]

very useful, Thanks Dan

[@dansfera]

thanks!

[@BucurEST1989]

Thank you

[@Christyle09]

Very helpful, Dan! Thank you. I’m taking notes.

[@dansfera]

thanks, good luck at your new job!

[@odwarotobias706]

What is the minimum for a site to be activated?

[@dansfera]

Irb approval and all docs. One week.

[@gadeboye2001]

How do you conduct a typical " Protocol Training" is there a format given by the Sponsor

[@dansfera]

Sometimes but usually is just a training however the cra sees fit and documented as per sponsor or cro sop

[@umairamin1229]

@@dansfera Can you elaborate on this, please? I'm thinking, "how do you conduct protocl training in 30 minutes?" Thanks.

[@HeyyyItsEdgar]

@@umairamin1229protocol overview, primary endpoints, safety training, device management and set up, documentation could be covered in that time

[@reyyajacob1049]

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]

Usually yes

[@zouhairallali6414]

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